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<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[以AQ膜中沉积铂的玻碳电极为基底的葡萄糖传感器]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930519]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[纪学锋,章咏华]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930519]]></guid><cfi:id>84</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[红细胞膜骨架蛋白的制备及其形态学观察]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930520]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[方芳,潘华珍,潘延]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930520]]></guid><cfi:id>83</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[高效液相色谱分析生物膜磷脂]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930521]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[汤习锋,康格非,曾成鸣]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930521]]></guid><cfi:id>82</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[微量Lowry法测定蛋白质含量]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930522]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[李红兵,李宗让,王志玲,孙连云]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930522]]></guid><cfi:id>81</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种通用高效的聚合酶链反应产物克隆方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930421]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[王亚新,陆佩华,周光炎]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930421]]></guid><cfi:id>80</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[尿蛋白快速SDS-PAGE测定及临床应用]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930422]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[唐志毅,许维桂,杨振华,黄一明,毛利民,吴华]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930422]]></guid><cfi:id>79</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[自旋捕集短寿命自由基的低温保存]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930423]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[丛建波,孙存普,莫简]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930423]]></guid><cfi:id>78</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[应用二次 PCR 技术提高体外基因扩增的效率]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930322]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[余伍忠,周常文,郝小军,魏静,李厚钧]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930322]]></guid><cfi:id>77</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种构建 cDNA 文库时 Sepharose CL-4B 筛分 cDNA 的简化方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930323]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[汪洛,张迺蘅]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930323]]></guid><cfi:id>76</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[用4,4′-二羧酸-2,2′-二喹啉测定红细胞膜蛋白]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930225]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[汪洪亮]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930225]]></guid><cfi:id>75</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[乙醇对超氧化物歧化酶活性邻联〔二〕茴香胺染色法的影响]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930226]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[张爱群,沈文梅]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930226]]></guid><cfi:id>74</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[关于提高 PCR 产物克隆效率的一些问题]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930227]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[王志珍]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930227]]></guid><cfi:id>73</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[电泳图谱的袖珍计算机描绘方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930123]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[黄亚军,徐媛]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930123]]></guid><cfi:id>72</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[自身红细胞制备凝血活酶测定凝血酶原时间]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930124]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[朱世银,王红英,于建华,李锡贵]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930124]]></guid><cfi:id>71</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种简便的凝胶干燥法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930125]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[叶淑金,陈小红]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930125]]></guid><cfi:id>70</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[反相高效液相色谱荧光法测定血清中过氧化脂质]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930126]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[李克,胡心宝]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19930126]]></guid><cfi:id>69</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[提高PCR产物克隆效率的几种途径]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940526]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[从提高PCR产物纯度，增加产物特异性入手，较详细地分析了影响PCR产物克隆效率的四个主要因素，并就每种影响因素给出了较为详尽的提高克隆效率的途径．]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[史艳红,赵世民,孙勇如]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940526]]></guid><cfi:id>68</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[肝素的定量法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940423]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[根据核糖核酸酶水解核糖核酸时，在300nm波长处光吸收值下降的速率被肝素抑制之特点，用已知量肝素对抑制程度进行定量，制得标准检量线，从而测得未知量的肝素含量．此法简捷方便，一次能测定多个样品．]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[张昌敬,黎义和,李贤柏]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940423]]></guid><cfi:id>67</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[极谱氧电极法测定超氧化物歧化酶活性的改进]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940424]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[对SOD的极谱氧电极测定法做了如下修改:a.室温测定,b.酶活性用标准SOD标定,c.反应在磷酸缓冲液中进行,d.增大邻苯三酚的用量.改进后克服了易在电极薄膜表面产生气泡等问题,测定灵敏度及线性范围增大.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[张继全,陈幼春,邹岳奇,阎静辉]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940424]]></guid><cfi:id>66</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种快速检测β－半乳糖苷酶活性的试纸方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940324]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[建立了一种检测β-半乳糖苷酶活性的5-溴-4-氯-3-吲哚-β-半乳糖苷(X-gal)试纸方法,其原理在于酶色原底物X-gal在β-半乳糖苷酶作用下产生蓝色5-溴-4-氯-吲哚.此方法X-gal用量少、操作简便、省时.适用于基因克隆的检定.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[袁素莉,付立,张其玖]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940324]]></guid><cfi:id>65</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[AST同工酶的琼脂糖凝胶电泳NBT显色法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940325]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[分布于细胞内线粒体及细胞质中的天门冬氨酸氨基转移酶(AST·EC·2·6·1·1)是人血清中含有的两种同工酶,分别称为AST-m和AST-c同工酶.AST-c电泳迁移率介于血清α-球蛋白与β-球蛋白之间.AST-m电泳迁移率相似于γ-球蛋白,琼脂糖凝胶电泳固蓝B染色法对m-AST检出率较低.用NBT显色法则可得到较好效果.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[石玉玲,陈彦红,刘讯]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940325]]></guid><cfi:id>64</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[用Fura－2双波长荧光法测定神经细胞内游离钙]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940326]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[采用新型Ca<sup>2+</sup>荧光指示剂Fura-2建立双波长荧光法测定分离的大鼠神经细胞内游离钙浓度([Ca<sup>2+</sup>]<sub>i</sub>).结果显示,在静息状态下,其[Ca<sup>2+</sup>]<sub>i</sub>为109±12nmol/L.30mmol/L KCl可显著增加[Ca<sup>2+</sup>]<sub>i</sub>,并且KCl的这种效应呈一定的剂量依赖关系,提示该法灵敏、可靠.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[卢步峰,黄诒森,鲁友明]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940326]]></guid><cfi:id>63</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[聚焦色谱法测定肌型肌酸激酶亚型]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940123]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[报道了测定CK-MM亚型的聚焦色谱法，此法简单，快速，结果可靠，线性范围宽，最低检测限（8U／L）较正常参考值低，比国外报道的类似方法高6倍以上，分离度亦有改进.测定了20例健康人血清亚型分布，与文献报道结果相近.该法自动化程度高，已在急性心梗的诊断中实际应用.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[孔庆银,杨振华,杨树德,唐志毅]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19940123]]></guid><cfi:id>62</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[从cDNA文库中筛选分析阳性克隆的简便方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950623]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[cDNA文库中阳性克隆的传统筛选分析法既费时又费力.利用微波炉加热的方法,简化了原位杂交中噬菌斑裂解、DNA变性与固定的程序;进一步运用PCR扩增技术,特异扩增克隆载体中插入的cDNA片段,加快了阳性克隆分析的进程.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[周兆斓,朱祯,刘春明,肖桂芳,李向辉]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950623]]></guid><cfi:id>61</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[PCR－SSCP分析实践]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950523]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[介绍了一种在一般实验室都能使用的适用于SSCP分析电泳的改良方法．并对如何设计引物、选择PCR条件和分析结果进行了讨论．]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[蔡辉国,陈佩贞,张立冬,彭琼,纪新军,马双]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950523]]></guid><cfi:id>60</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[PCR－SSCP检测肺癌细胞p53基因点突变]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950524]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[应用溴化乙锭(EB)染色的PCR-SSCP技术对10例非小细胞性肺癌组织标本p53基因外显子5～8进行分析,其中1例在外显子5～6;1例在外显子7;2例在外显子8发现异常电泳带.对1例经SSCP检测异常的p53基因进行核酸序列分析,发现第280位密码子由AGA变成ACA,其编码的氨基酸由丝氨酸变成半胱氨酸.结果证实:非小细胞性肺癌与p53基因突变有关;EB法PCR-SSCP技术是一种简便、可靠的点突变检测法.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[毕向军,彭朝晖,李金翰,杨光彩,徐湘民,王红]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950524]]></guid><cfi:id>59</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[细胞内RT－PCR扩增免疫球蛋白重链可变区基因]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950424]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[通常,逆转录PCR(RT-PCR)需要高质量的mRNA,操作过程复杂,效率低且易受到RNase的破坏,为了简化操作,提高效率,用10%甲醛盐溶液固定杂交瘤细胞,以Np-40渗透化处理细胞后做RT-PCR,获得了大约350bp的特异性免疫球蛋白重链可变区基因片段,与用同一对引物得到的常规RT-PCR扩增产物一致.这项技术可用于获得特定结构基因片段,连结并扩增嵌合蛋白基因及构建多克隆免疫球蛋白文库等.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[李昌龙,赵满仓,王抒,蒋雷,李健斋]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950424]]></guid><cfi:id>58</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种转移非特异性蛋白带的染色方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950425]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[考马斯亮蓝是常用的聚丙烯酰胺凝胶蛋白电泳的染料,利用硝酸纤维素膜(NCF)对染料的吸附作用,将低浓度的考马斯亮蓝(0.025%)染色液直接对NCF上的转移蛋白带进行染色,经实验反复验证.它是一种较好的NCF上转移非特异性蛋白带的染色方法.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[夏另朝,李金照,陈燕]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950425]]></guid><cfi:id>57</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[人肝脏特异的F抗原分离纯化及其抗血清制备]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950223]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[取新鲜的人肝脏，充分洗涤，制备匀浆，上清液经Sephadex-G200、DE52层析，聚丙烯酰胺凝胶电泳，得到电泳纯Ｆ抗原，并免疫制备抗血清.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[汪俊军,赵仲农,庄一义,邱廷刚,陆炜]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950223]]></guid><cfi:id>56</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种简单、快速、经济的mRNA分离方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950224]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[对oligo(dT)纤维素纯化poly(A)RNA的方法进行了改良.缩小了层析柱床的体积,使填料用量仅为常规量的1/50-1/100,即在移液器尖嘴中进行层析.与常规方法相比,它具有实验时间短、洗脱的mRNA可直接合成cDNA和得率较高等优点.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[王易伦,戴建新,郭瀛军,陆德如]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19950224]]></guid><cfi:id>55</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[考马斯亮蓝显色液组分对蛋白质测定的影响]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960622]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[考马斯亮蓝（CBB）显色法测定蛋白质含量的主要缺点之一是线性关系差．通过研究显色液组分对线性关系的影响，发现显色液H<sup>+</sup>浓度是影响线性关系的主要因素，并提出了一个新的显色液配方来改善考马斯亮蓝蛋白质测定法的线性关系．]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[郭敏亮,姜涌明]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960622]]></guid><cfi:id>54</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[鼠肝抽提液中磷酸酶活性终止方法的改进]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960623]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[改进了一种分析磷酸酶活性的终止酶反应方法.该方法通过在酶反应进行到一定程度时，在反应混合物中加入酶反应终止液(1mol/L NaOH-0.2mol/L EDTA)，从而使测定更简捷、精确.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[梁智群,李相萍,杨胜远]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960623]]></guid><cfi:id>53</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[高效液相色谱法测定超滤后血浆中的谷氨酰胺]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960522]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[用高效液相色谱法测定超滤后血浆中的谷氨酰胺, 平均回收率为96.75%, 在130～1300μmol/L范围内呈线性关系(<i>r</i>=0.9906), 健康人正常值男性为(694.97±102.31)μmol/L, 女性为(623.79±99.27)μmol/L, 男女间值有显著差别(<i>P</i>＜0.05)该分析方法简单、迅速, 可用于外科肠道内营养的监测和对肠粘膜结构与功能的研究.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[刘放南,盛学勤,陈永明]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960522]]></guid><cfi:id>52</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种构建重组杆状病毒的简易方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960523]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[对传统构建重组杆状病毒的方法作了如下改进：先用磷酸钙共沉淀法单独将质粒DNA转进昆虫Sf细胞中，其中重组质粒采用聚乙二醇沉淀法纯化，12～24h后再用低剂量的病毒攻击细胞．改进后的方法简便、省时、经济、重组率高，适于一般实验室使用．]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[李迎秋,施先宗,吴文言,龙綮新,王珣章]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960523]]></guid><cfi:id>51</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[基因组YAC文库构建方法的几点改进]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960426]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[以pJS97、pJS98为载体, 对中国人基因组YAC文库的构建进行了尝试.建立了一种对小片段DNA“原位电泳筛除”的方案, 采用多胺溶液处理以减少大片段DNA的降解, 使整个建库工作更加简便、有效. 此外, 改进了转化子的挑取和保存的方法, 既简化了操作, 又减少了杂菌污染和交叉污染. 这些改进的方案, 可以推广到其他高等生物基因组YAC文库的构建和应用工作.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[杨智勇,匡达人,黎伶俐,陆劭,宋明浩,戴和平,龙志高,潘乾,李麓芸,夏家辉]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960426]]></guid><cfi:id>50</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[快速检查寡聚DNA片段序列的方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960324]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[以质粒为模板，用待测寡聚DNA片段和通用测序引物进行PCR（聚合酶链式反应），PCR片段经纯化后插入到pUC－18或pUC－19的多克隆位点中，然后用通用测序引物测定重组质粒上待测寡聚DNA片段，即可清晰、正确地知道它的序列．]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[朱榴琴,吴宇杰]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960324]]></guid><cfi:id>49</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种简便经济的凝胶电泳同工酶特异染色方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960223]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[介绍一种简单、经济的同工酶染色方法：用熔化的0．4％琼脂糖处理滤纸备用，染色前将滤纸浸于同工酶染色液中，染色时将滤纸盖在聚丙烯酸胺胶上，然后将胶放在有盖塑料盒中保温染色，染色时间要比普通方法略长。染色后将胶和滤纸移入固定液中用镊子除去滤纸．]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[杨凯,尚忠林]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960223]]></guid><cfi:id>48</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[比色法测定Fenton反应产生的羟自由基]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960224]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Fenton反应产生的羟自由基能与水杨酸生成羟基化产物2，3－二羟基苯甲酸，用比色法测定其含量能间接测定羟自由基的生成量．通过对测定条件的研究，得到最佳的测定方案．可作为一种简便的筛选羟自由基清除剂的方法]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[贾之慎,邬建敏,唐孟成]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960224]]></guid><cfi:id>47</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[PCR扩增TCRVδ2－Dδ3片段的临床价值]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960125]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[以巢式PCR扩增急性淋巴细胞白血病细胞中TCRVδ2－Dδ3重排片段，同时将生物素掺入初诊期骨髓标本扩增产物中，标记成患者克隆特异性探针，通过点杂交法检测缓解期患者体内残留的白血病细胞．结果提示该法对于临床病情监测有一定的价值．]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[李昕权,郑敏,李昕跃]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960125]]></guid><cfi:id>46</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种鉴定过氧化氢酶活性的铁染色法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960126]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[采用聚丙烯酰胺凝胶电泳(PAGE)技术，建立了一种新的鉴定过氧化氢酶活性的方法──铁染色法．结果表明，细菌过氧化氢酶及牛肝过氧化氢酶显示单一的酶活性带．该方法操作简单、快速、灵敏度高、专一性强.是一种切实可行的鉴定过氧化氢酶活性染色法.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[董泗建,刘昌玲]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19960126]]></guid><cfi:id>45</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[核酸探针与酶免疫反应板定向结合的方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19970423]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[为了制备一种可供寡核苷酸探针定向结合的酶免疫反应板, 利用部分水解的尼龙包被酶免疫反应板,通过尼龙所含的氨基基团与寡核苷酸探针所含的5′磷酸基团,在水溶性碳二亚胺的催化下,与酶免疫反应板发生5′端特异性定向共价结合, 并对肺炎支原体的PCR扩增产物进行了重复检测,结果重复性好,方法稳定.利用该方法制备的酶免疫反应板可用于核酸探针的临床检测.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[刘吉荣,吴婉芳,秦雨春,张玉,马官福]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19970423]]></guid><cfi:id>44</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[改善大分子质粒DNA重组效率的新方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19970322]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[采用两次连接法对一个质粒载体为7.65 kb，插入子为1.47 kb的片段进行重组连接，使连接效率大大提高.此方法对于大分子的质粒DNA重组是非常有效的.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[谭德勇,邓双胜,孟玲,昝瑞光]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19970322]]></guid><cfi:id>43</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[PSⅡ反应中心D1蛋白的小肽抗体的制备和鉴定]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19970323]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[用人工合成的PSⅡ反应中心D1蛋白中(229～240)的12肽,与牛血清白蛋白偶联后做为抗原免疫家兔, 获得抗菠菜D1蛋白抗体. 免疫双扩散法测得其具较高的效价，蛋白印迹检测结果显示该抗体仅与D1蛋白有免疫亲和反应. 表明此抗体可作为检测D1蛋白及其光抑制时降解产物的探针.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[李晓鹏,杜林方,梁厚果,吴宛荪]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19970323]]></guid><cfi:id>42</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[激活淋巴细胞cDNA单链库的构建]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19970121]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[介绍一种激活淋巴细胞cDNA单链库构建方法,此库具有良好的模板活性. 用PCR法从此库中克隆了多种中国人源性的细胞因子.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[范灵芝,刘彦仿,杨新科,候云德]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19970121]]></guid><cfi:id>41</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[利用SADF法进行家蚕基因组DNA多态性分析]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19980621]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[从家蚕品种C108和大造后部丝腺提取的基因组DNA，用<i>Pst</i>Ⅰ酶解后与自己设计的人工接头相连，并用与人工接头序列相匹配的选择性引物进行选择性PCR扩增(selective amplification).扩增产物经琼脂糖电泳检测显示，用SADF法在两品种中能检测到稳定的DNA多态性片段.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[何宁佳,鲁成,周泽扬,向仲怀]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19980621]]></guid><cfi:id>40</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[甲肝病毒减毒株(H<sub>2</sub>)RNA的全长RT-PCR扩增]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19980521]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[通过RT-PCR技术扩增了甲肝病毒减毒株(H<sub>2</sub>)全长RNA,并对长片段RT-PCR扩增进行了方法学上的探讨.采用抗血清特异沉淀病毒;盐酸胍-酸性酚、氯仿一步法分离纯化病毒RNA,可得到高质量的RNA样品;以此RNA为模板,在无RNA酶的逆转录酶作用下,合成单链cDNA;继续以此cDNA为模板,利用32 mer寡核苷酸引物, 在Taq和Deep Vent DNA多聚酶的作用下进行PCR扩增,得到7.4 kb的扩增产物.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[周翔,谭德勇,赖建华,昝瑞光]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19980521]]></guid><cfi:id>39</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[用低浓度硫氰酸胍提取高质量植物RNA]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19980423]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[目前分离RNA的方法很多, 但大多是基于动物材料建立的方法, 而针对植物材料的方法并不多见. 建立了一种从植物材料中分离高质量RNA的硫氰酸胍/氯化锂/热酚法. 与其他硫氰酸胍的方法相比, 该方法所用硫氰酸胍的浓度仅为现有方法的1/40 (0.1 mol/L),降低了实验成本, 且所得RNA质量令人满意. 用该方法分离的RNA在琼脂糖凝胶电泳上可清晰分出4条核糖体RNA (rRNA)带; 用此RNA进行RNA印迹或分离mRNA进行体外翻译试验, 均获得很好效果.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[何军贤,梁厚果]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19980423]]></guid><cfi:id>38</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种改进的融合蛋白亲和层析纯化方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19980324]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[用马铃薯淀粉柱可以直接分离麦芽糖结合蛋白-乳酸脱氢酶辅酶结合结构域融合蛋白，并得到满意的结果.它提纯的程度和吸附量都和商品交联直链淀粉亲和层析柱相比拟，但是成本却要低很多，而且从市场上买来的马铃薯淀粉就可以应用.它可以成为大规模生产的一种工艺路线.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[廉德君,许根俊]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19980324]]></guid><cfi:id>37</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[噬菌体DNA的快速抽提]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19980225]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[介绍一种噬菌体DNA的快速抽提方法.用聚乙二醇沉淀噬菌体颗粒，然后经DEAE纤维素纯化处理和酚抽提.与传统的噬菌体DNA纯化方法相比，改进后的方法方便、快速、经济，可获得高纯度的噬菌体DNA.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[覃文新,万大方,赵新泰,蒋惠秋,顾健人]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19980225]]></guid><cfi:id>36</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种抑制pGEX载体系统本底表达的方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19980123]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[用pGEX载体系统体外构建了一种人精子膜蛋白片段（HSDⅡ）的重组表达质粒.未经IPTG诱导，该质粒表达的融合蛋白在DH5α中即有较高的本底表达量.若将带有LacⅠ基因的pREP4质粒与重组表达质粒共转化DH5α菌，则可有效抑制融合蛋白的本底表达.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[黄蓬,缪时英,王琳芳]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19980123]]></guid><cfi:id>35</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[共价连接的多肽酶联免疫测定法的研究]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990627]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[采用紫外线照射及戊二醛活化处理聚苯乙烯酶标板后再包被八肽胆囊收缩素（CCK-8），以此为基础进行酶联免疫吸附试验（ELISA），通过不同的洗涤过程对CCK-8与酶标板相互作用的性质进行研究.结果表明，该包被方法可使CCK-8通过共价交联的方式稳定地结合于固相载体上，该方法适用于不同来源的酶标板，处理后的酶标板性质稳定，可储存使用，测定的批内及批间变异系数分别为4.75%和7.80%，方法稳定可靠，重复性好，便于推广应用.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[何涛,陈曼玲]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990627]]></guid><cfi:id>34</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[胰蛋白酶的高压灭菌]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990430]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[胰蛋白酶在酸性条件下经过高压灭菌，仍有活力.在细胞培养中，以这种方法对胰蛋白酶消毒比常规的过滤除菌更加简便，经济，安全可靠.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[何元政,刘定干]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990430]]></guid><cfi:id>33</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[英特网上生物信息资源的利用]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990330]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[充分利用英特网上完善的生物信息资源是十分有益且必要的.介绍了利用网上生物资源的几种主要方式和一些重要的站点和生物信息搜索引擎.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[李勇,倪福太,贺福初]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990330]]></guid><cfi:id>32</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[温度梯度凝胶电泳技术及应用]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990331]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[温度梯度凝胶电泳（TGGE）是一种用于检测核酸序列变异和点突变的电泳方法.该法利用不同构象的核酸分子具有不同的变性温度（<i>T</i><sub>m</sub>)来进行分离.TGGE方法具有分辨能力高、重复性好和节省时间的特点，可广泛应用于分子生物学研究领域.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[陈汉奎,冯忻]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990331]]></guid><cfi:id>31</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种用分光光度计检测氧自由基的新方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990225]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[报告检测过硫酸铵／N, N,N′,N′-四甲基乙二胺体系所产生的氧自由基的新方法.O<sup><sup>-</sup><sub>·</sub></sup><sub>2</sub>与羟胺溶液反应生成NO<sup>-</sup><sub>2</sub>，NO<sup>-</sup><sub>2</sub>经对氨基苯磺酸和α-萘胺显色在波长530 nm处有专一吸收峰，其颜色深浅与产生的O<sup><sup>-</sup><sub>·</sub></sup><sub>2</sub>呈量效关系.氧自由基清除剂抗坏血酸对O<sup><sup>-</sup><sub>·</sub></sup><sub>2</sub>的清除作用也呈明显的量效关系.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[萧华山,何文锦,傅文庆,曹红云,范子南]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990225]]></guid><cfi:id>30</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[山羊小腔卵泡DNA含量的荧光分析]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990226]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[用显微手术法剥离山羊3 mm以下完整小腔卵泡,用胶原酶和Triton X-100进行处理,选用荧光试剂4,6-二脒基-2-苯吲哚(4,6-diamidino-2-phenylindol-2HCl,DAPI),对其DNA含量进行分析.结果表明,山羊3 mm以下卵泡的DNA含量与卵泡直径相关性极显著(<i>r</i>=0.9824＞0.7800=<i>r</i><sub>0.01</sub>,<i>n</i>=12).该法可测定5 ng的DNA.提示该法在卵泡生长发育的研究中具有重要应用价值.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[李键,康靖全,周乐,王建辰]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990226]]></guid><cfi:id>29</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[液泡膜H<sup>+</sup>-ATPase质子泵活性的荧光测定]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990227]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[使用荧光猝灭法测定植物液泡膜H<sup>+</sup>-ATPase质子转运活性. 比较了两种常用荧光染料吖啶橙和喹亚因在不同浓度的测定灵敏度. 探讨了不同蛋白量和缓冲系统对测定结果的影响. 得到了用5 μmol/L吖啶橙，200～250 μg蛋白质含量，Hepes-Tris(pH 7.0)为缓冲介质，ATP-Na为底物的最适体系.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[王欢,祝雄伟,王延枝]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990227]]></guid><cfi:id>28</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种PCR产物克隆的新方法——T-A克隆法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990228]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[介绍一种PCR产物克隆的新方法——T-A克隆法. 用改良碱裂解法抽提pBluescript SK(+)质粒，用<i>Eco</i>RⅤ将pBluescript SK(+)质粒切成平端，利用Taq DNA聚合酶及dTTP制备pBluescript SK(+) T-A载体. 将β-actin cDNA片段克隆入自制的pBluescript SK(+) T-A载体，经<i>Eco</i>RⅠ及<i>Hin</i>dⅢ双酶切得到与设定长度一致的β-actin cDNA片段.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[李新波,赵小松,田德志,朱依纯,姚泰]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990228]]></guid><cfi:id>27</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[细胞色素P450 2D6酶缺陷等位基因的分析]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990126]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[细胞色素P450 2D6(CYP2D6)第1 795位胸腺嘧啶核苷缺失造成CYP2D6酶活性缺陷，该等位基因被称为CYP2D6T.对该等位基因的测定有助于准确预测CYP2D6表现型.利用等位基因特异扩增法的基本原理，建立了测定CYP2D6T的方法.经396例测定，证明比利用PCR扩增后再酶切的方法更为快捷、更少污染，为该项测定应用于临床奠定基础.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[陈枢青,孙红颖,赵鲁杭,P.J.WEDLUND]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/19990126]]></guid><cfi:id>26</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[应用T/A策略克隆乙肝病毒pC/C及C基因]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000623]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[以克隆乙型肝炎病毒pC/C及C基因为例，报道了在DNA重组中，当目的基因与载体末端不匹配时可采取的一新方法.用内切酶切取的基因片段为平端时，可在含dATP的反应体系中，用Taq酶的末端转移酶活性在其3′末端加上单个碱基(dA)的突出尾；基因片段为3′凹端时，可在含4种dNTP的体系中，利用Taq酶的聚合酶活性先将其末端补平，再经末端转移酶活性在其3′末端加dA尾；末端经此修饰的基因片段可亚克隆至T载体中，再克隆于其他表达载体中.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[刘定燮,骆抗先]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000623]]></guid><cfi:id>25</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种简便的考马斯亮蓝G250蛋白质染色方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000529]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[介绍一种快速、简便、几乎无背景的考马斯亮蓝G250(CBB G250)染色方法.该方法所用试剂仅为稀盐酸和CBB G250, CBB G250的工作浓度为0.0015%，灵敏度达0.02 μg/带, 染色2 h达70%,4 h以上或染色过夜即可充分染色.与以往的考马斯亮蓝染色方法相比，该方法有经济方便、灵敏度高、几乎无背景等优点，便于推广应用.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[江南,吴开力,黄强,潘苏华]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000529]]></guid><cfi:id>24</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种改进的乳酸脱氢酶同工酶染色法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000430]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[以N-甲基吩嗪甲基硫酸盐（PMS）为介体，使乳酸脱氢酶（LDH）同工酶催化反应产生的NADH将铁氰化钾还原为亚铁氰化钾，利用亚铁氰化钾与三氯化铁反应生成普鲁士蓝的性质，实现对乳酸脱氢酶同工酶进行染色的目的.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[赵赣,张守全,黄肖武,詹福建,何安行]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000430]]></guid><cfi:id>23</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[转移缓冲液对蛋白质印迹的影响]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000328]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[利用三种转移缓冲液，分别以半干和湿转法，检测癌基因产物Bcl-2, 并获得不同强度的印迹结果.不含SDS的转移缓冲液转移效果明显优于含SDS的转移缓冲液，且SDS含量越高印迹带越弱；此外，半干转移与湿转相比，可大大缩短转移时间，但转移效果不及湿转理想且稳定性较差.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[周建,王小行,高小平]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000328]]></guid><cfi:id>22</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[PCR产物末端性质的分析研究]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000228]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[利用PCR、UT-PCR、克隆及测序等技术，对强直性肌营养不良基因（MT-PK）3′-非翻译区分别用Taq，Taq＋Pwo DNA聚合酶进行了扩增、克隆和测序，研究了PCR产物末端组成情况，并比较了上述两种DNA聚合酶对PCR产物末端的影响.结果在用Taq DNA聚合酶扩增的PCR产物主要得到3′端突出1个A（占67.3％，35/52）；在Taq＋Pwo DNA聚合酶扩增的PCR产物末端中得到3′端+A的仅占17.4％，而－1的占34.8％，与前者显著不同.表明PCR扩增产物的末端是复杂多样的.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[夏庆杰,张思仲,武辉,肖翠英]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000228]]></guid><cfi:id>21</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[T细胞亚群CD4测定方法的研究]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000229]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[为比较外周血T淋巴细胞亚群CD4不同测定方法的差别，以流式细胞术为定量手段，测定了猴外周血中三种不同方法处理后CD4的表达.结果表明：先标后溶法——先用异硫氰荧光素标记的单克隆抗体（FITC-CD4 McAb）标记后，再加入红细胞溶解液溶掉红细胞的处理方法，结果基本等同于传统的淋巴细胞分离法，但样本用量仅为传统方法的1/5，且操作简单.激光共焦显微术的形态学研究也证实：先标后溶法与淋巴细胞分离法相似，其细胞膜表面荧光标记清晰，优于先溶后标法.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[韩梅,吕平,何其华,袁兰,马士良,陶家平]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000229]]></guid><cfi:id>20</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[两步PCR快速扩增东亚钳蝎BmKIT3 3′cDNA末端序列]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000125]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[对3′-RACE方法进行了修改，采用一条特异性引物和一条通用Oligo dT引物成功地克隆了东亚钳蝎BmKIT3 3′cDNA末端，与常规3′-RACE方法相比，两步PCR方法具有节约成本、节省时间、增加反应特异性等优点，尤其适用于生物活性肽基因的快速克隆和鉴定.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[朱顺义,李文鑫]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000125]]></guid><cfi:id>19</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种快速简便的CaCl<sub>2</sub>质粒转化方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000126]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[介绍一种质粒DNA快速转化方法.质粒DNA加入感受态细胞，冰浴３～10 min，涂布预热至37℃的平板，即可获得与常规转化方法相当的转化效率.操作步骤由5步减至2步，时间由2 h减至3～10 min.同时探讨了Ca<sup>2+</sup>浓度、4℃保存时间等因素对感受态细胞转化效率的影响.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[肖庚富,齐义鹏,李莉,易巍]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000126]]></guid><cfi:id>18</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种改进的蛋白质超薄凝胶电泳方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000127]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[介绍了一种将聚丙烯酰胺凝胶固定在电泳夹板上的蛋白质电泳方法.通过此方法蛋白质电泳可以在0.4 mm厚的聚丙烯酰胺凝胶上进行.实验证明，经此方法处理的玻板结合凝胶非常牢固，在电泳后的所有处理步骤中都不会发生凝胶脱落现象.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[郭泽坤,张涌]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20000127]]></guid><cfi:id>17</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[活化海绵镉微型柱层析法测定血清中一氧化氮]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010432]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[采用铜离子活化海绵镉微型柱层析法将血清中的硝酸盐(NO<sup>-</sup><sub>3</sub>)还原为亚硝酸盐(NO<sup>-</sup><sub>2</sub>)，再通过Griess反应测定NO<sup>-</sup><sub>3</sub>/NO<sup>-</sup><sub>2</sub>总量以反应体内一氧化氮（NO）水平，从而建立血清NO间接测定新方法. 结果表明，在pH 9.7 时，活化海绵镉还原NO<sup>-</sup><sub>3</sub>能力强、速度快、抗干扰性好，还原率为96.4%～100.0%，检测范围为0～400 μmol·L<sup>-1</sup>，检测限为1.85 μmol·L<sup>-1</sup>，相对标准偏差为2.56%～3.46%，对NO<sup>-</sup><sub>3</sub>的回收率为96.4%～102.2%，对NO<sup>-</sup><sub>2</sub>的回收率为95.2%～101.3%，对混合标准液的回收率为98.7%～104.4%.该方法具有简便快速、灵敏准确、样品和试剂用量小等优点，可在临床推广应用.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[邓健,吕昌银,张建明,袁亚莉]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010432]]></guid><cfi:id>16</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[溶血栓酶活性测定的一种新方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010433]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[根据血栓溶解会引起吸光度下降的特性，在细胞培养板上制作小血栓，利用酶标仪同时检测多个样品的吸光度变化.发现反应初期，血栓吸光度的降低同时间呈线性关系，其回归方程的斜率<i>k</i>与酶活性成正比.因此可用<i>k</i>来表示酶活性.此方法与蛋白凝块溶解时间法(CLT法)相关性很好.该法省时，成本低，是一种较好的、实用的检测溶血栓酶活性的方法.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[谢秋玲,林剑,张玲]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010433]]></guid><cfi:id>15</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[从矿化的骨组织中提取骨细胞的总RNA]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010434]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[描述了两个从以含大量羟基磷灰石（钙）和细胞密度、数量甚低为特点的矿化的成年骨组织（成年大鼠颅骨）提取总RNA的改进方法.紫外分光光度法（<i>A</i><sub>260</sub>、<i>A</i><sub>280</sub>和<i>A</i><sub>230</sub>）和1%甲醛变性琼脂糖凝胶电泳予以鉴定.进而以其逆转录的cDNA为模板扩增出β-actin和BMP-2基因，均表明所得总RNA完整和模板活性俱佳.每克骨组织中总RNA产量为560 μg.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[郭若霖,郭善一,左爱军,梁东春,张镜宇]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010434]]></guid><cfi:id>14</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[固相DNaseⅠ足迹法研究DNA-蛋白质相互作用]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010435]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[传统的DNaseⅠ足迹法程序繁杂，并且要求目的蛋白经过一定程度的纯化.而固相DNaseⅠ足迹法通过结合有模板的磁珠，先富集序列特异的DNA结合蛋白，进行DNaseⅠ酶切，然后用测序胶分离并分析结果.此方法简便易行，重复性好，并减少了对操作者的放射性损害，尤其适用于研究未经纯化的核蛋白粗提物内序列特异蛋白.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[徐冬冬,刘德培,吕湘,徐海明,张伸,梁植权]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010435]]></guid><cfi:id>13</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[用任意引物PCR进行基因多态性分析时最佳反应条件的建立]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010436]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[用任意引物进行基因组指纹分析是检测DNA多态性的一种通用方法，对遗传学图谱绘制、系统发育学和种群生物学都很有用.由于任意引物PCR(AP-PCR)影响因素很多，获得理想的指纹扩增图谱比较困难,有必要寻找一种简单有效的方法建立最佳扩增体系.对Mg<sup>2+</sup>浓度，模板浓度、引物浓度等三个因素进行优化选择AP-PCR扩增反应实验研究.实验结果表明：Ap-PCR反应的最佳反应条件为2 mmol/L MgCl<sub>2</sub>,50 ng的DNA模板及0.3 μmol/L的引物浓度，在上述条件下获得的AP-PCR产物最丰富，条带清晰.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[艾斯卡尔·依米提,哈木拉提·吾甫尔,伊力哈木江·沙比提]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010436]]></guid><cfi:id>12</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[毛细管电泳-激光诱导荧光分析血清多胺的研究]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010335]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[为进一步探讨多胺的生物学作用，建立了毛细管电泳-激光诱导荧光(<i>λ</i><sub>ex</sub>=488 nm,<i>λ</i><sub>em</sub>=513 nm)分析血清多胺方法.在碱性介质中，多胺与荧光素异硫氰酸酯进行衍生化反应，硼酸盐(pH 8.6)作为运行缓冲液，运行电压20 kV，腐胺、精胺、精脒和1，6-己二胺（内标）在8 min内达到基线分离.考察了方法的线性范围、稳定性、检测限和方法的回收率等，方法具有样品处理简单，灵敏度高，速度快等特点.用于正常对照大鼠和肿瘤大鼠血清多胺的测定.结果提示：实验组肿瘤大鼠血清精胺和精脒水平显著高于正常对照大鼠和实验组未出现肿瘤大鼠血清精胺和精脒水平（<i>P</i>＜0.05），正常对照组大鼠和实验组未出现肿瘤大鼠血清精胺和精脒水平间无显著性差异（<i>P</i>＞0.05），各组间血清腐胺水平均无显著性差异（<i>P</i>＞0.05）.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[张振中,吴逸明,程维明,吴如金]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010335]]></guid><cfi:id>11</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[基于PC/Linux的核酸序列分析系统的构建及其应用]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010231]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[基于PC机和Linux操作系统, 利用Phred/Phrap/Consed软件和Blast软件, 构建了核酸序列大规模自动分析系统. 该套系统可自动完成从测序峰图向核酸序列的转化、载体序列去除、序列自动拼接、重复序列鉴定以及序列的相似性分析, 可加速对大规模测序数据的分析和利用.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[张成岗,欧阳曙光,张绍文,瞿祥虎,鱼咏涛,周钢桥,吴松锋,贺福初]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010231]]></guid><cfi:id>10</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[固定化镍离子亲和层析胶的制备及其性能鉴定]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010232]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[以Sepharose 6B为原料，在强碱性条件下用环氧氯丙烷活化，再与亚氨基二乙酸（IDA）的钠盐溶液反应，在活化好的胶颗粒表面接上很多手臂IDA；最后与硫酸镍溶液反应，使手臂IDA与Ni<sup>2+</sup>发生螯合反应，即得到固定化Ni<sup>2+</sup>亲和层析胶（Ni<sup>2+</sup>-IDA）.采用原子吸收法及从大肠杆菌表达产物中纯化重组人B淋巴细胞刺激因子（hBLyS）等方法检测制备胶的理化指标和纯化蛋白质的性能.结果表明用此法制得的亲和胶与相应商品胶的性能完全一致，而成本却不到商品胶的十分之一.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[刘平,张双全,闫晓梅,徐进曙]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20010232]]></guid><cfi:id>9</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[丝胶蛋白粉末的制备及其应用于L-天冬酰胺酶的固定化]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20020628]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[蚕丝蛋白经高压高温水脱胶后所得的丝胶溶液，经过纯化、浓缩以及喷雾干燥，制成丝胶蛋白粉末.这种丝胶蛋白分子质量高达200 ku，其粉末呈白色，平均粒度10 μm，为热水溶性蛋白.以这种丝胶蛋白粉末为载体，用戊二醛为交联剂，制成固定化L-天冬酰胺酶.对这种固定化酶活性和动力学性质进行初步研究和分析，结果表明这种固定化酶性能稳定，对热的稳定性有所提高，并具有较好的操作稳定性，抗胰蛋白酶水解能力大大提高.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[陶美林,张雨青,沈卫德,王新波,张海萍,周文林,马燕]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20020628]]></guid><cfi:id>8</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[神经介素U(neuromedin U)研究概况]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20020534]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[郑旭煦,胡应和,欧阳克清,李新平,蔡绍皙]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20020534]]></guid><cfi:id>7</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种简单、快速筛选水稻种胚脂氧合酶-3缺失体的新方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20020533]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[根据水稻种胚脂氧合酶-3（LOX-3）催化产物的氧化特性，结合脂氧合酶的专一性抑制剂——去甲二氢愈创木酸，建立了筛选水稻种胚脂氧合酶-3缺失体的I<sub>2</sub>-KI比色法，并探讨其最佳实验条件.与常用的单克隆抗体筛选技术相比，该方法具有准确、简单且成本低的特点，可以进一步用于耐储藏水稻的育种研究.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[沈文飚,周彤,王益华,俞伟伟,郑天清,翟虎渠,万建民]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20020533]]></guid><cfi:id>6</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种安全制备活化琼脂糖树脂的方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20020234]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[溴化氰是常用载体(树脂)活化剂，但其毒性很强，具有挥发性，活化后树脂带较强的电荷而导致非特异性吸附.羰基二咪唑(1,1′-carboxyl-diimidazole, CDI)近年来被用于树脂的活化，具有毒性低、相对安全、方便、活化效率高、活化后树脂所带电荷相对较少等优点.由于国内同行很少采用CDI活化树脂制备亲和层析柱或固定化酶，在此介绍该方法的一些关键步骤供同行参考.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[伍学勤,吴岑,凌晓红,陈建文,赫荣乔]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20020234]]></guid><cfi:id>5</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[单质粒模式诱导表达载体系统的建立]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20030526]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[在Invitrogen公司T-Rex诱导表达系统的基础上，将目的基因与调控蛋白基因克隆于同一载体上，并在CV1细胞中观察了四环素对该单质粒模式载体报告基因表达的诱导效应.载体在瞬时转染CV1细胞并以四环素诱导24 h后目的基因的表达水平提高了8.9倍，表明单质粒模式载体基因诱导表达的应用具有可行性.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[刘定燮,周晓巍,黄培堂]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20030526]]></guid><cfi:id>4</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[一种经济、简便的双向电泳方法]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20030130]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[双向电泳是蛋白质分析的一门较为精确的技术.对电泳方法进行改良并采用普通垂直薄板等电聚焦技术，不仅大大降低了蛋白质双向电泳的成本，而且操作过程简单，是一种用于初步分析蛋白质的较好方法.在中华卵索线虫(<i>Ovomermis sinensis</i>)雌雄成虫可溶性差异蛋白的分析中获得了较满意的结果.这一改良方法的建立，可望促进双向电泳的广泛应用.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[高原,王国秀,刘中来]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20030130]]></guid><cfi:id>3</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[用改进的重叠PCR引入血管内皮生长因子基因突变]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20040216]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[血管内皮生长因子（vascular endothelial growth factor, VEGF）的PCR产物克隆于T载体上，经转化JM109感受态菌株后,随机挑取8个白斑菌落，混合后制成混合模板.采用3条引物，做两轮重叠PCR反应，获得了VEGF的突变基因，经PCR鉴定，酶切鉴定和测序分析表明所得基因为目的产物.实践证明这种突变方法简单快速，为下一步实验大量引入突变奠定了实验基础.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[白向阳,吕安国,吴文芳,孙静,牛瑞芳]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/20040216]]></guid><cfi:id>2</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[提取高质量人参RNA的方法研究]]></title>
<link><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/2005-0519]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[针对人参组织多酚、多糖类物质含量较高的特点，比较了改良的异硫氰酸胍法、改良的CTAB法和改良的Trizol法等3种不同的RNA提取方法. 3种改良的方法均能从人参组织中提取到总RNA. 其中改良的Trizol法能有效地抑制酚类物质和多糖对总RNA提取的影响，能从成熟的叶片中获得高质量、完整性好的总RNA，每克新鲜组织RNA产量在90～120 μg之间，电泳分析， 28 S rRNA亮度约为18 S rRNA的2倍，A260/A280介于1.8～2.0之间. 用改良的Trizol法分离的RNA，已成功进行了RT-PCR及人参叶cDNA文库构建等研究.]]></description>
<pubDate></pubDate>
<category><![CDATA[经验交流]]></category>
<author><![CDATA[王  昆,王  颖,鲍永利,孟祥颖,乌  垠,李玉新]]></author>
<guid><![CDATA[https://www.pibb.ac.cn/pibbcn/article/abstract/2005-0519]]></guid><cfi:id>1</cfi:id><cfi:read>true</cfi:read></item>
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