印迹

Polymerase chain reaction was performed on lesion scrapings, aspirates, and filter paper impressions.

对病灶进行刮除，抽吸和滤纸印迹并进行聚合酶链反应。

SDS-PAGE and Western blot of culture supernatant showed that hsIL-1RⅠ was secretively expressed. Recptor-ligand binding assays showed that the recombinant hsIL-1RⅠ has receptorligand binding activity.

发酵液经SDS-PAGE和Western blot证实分泌表达了sIL-1RI，经蛋白印迹受体配基结合反应证实分泌表达的sIL-1RI具有配基受体结合的生物学活性。

Tricine-SDS-PAGE and Western Blotting demonstrated that they could express ESAT-6 after heat induction either fused to BCG HSP60 or secretively into the culture filtrate, respectively.

Tricine-SDS-PAGE和免疫印迹证实这两株重组卡介苗经热诱导后分别能融合表达或分泌表达ESAT-6。

Secondly, Northern blot showed that OsBP-73 was weakly expressed in root, leaf and immature seed.

Northern印迹结果表明OsBP-73基因在水稻根，叶片和未成熟种子中均有较低水平的表达，而且在各组织中的表达没有明显的差异。

In addition the absorption and selective recognition ability of Tri-MIPs to trichlorfon was studied and its structure was charicterized.

测定分子印迹聚合物对敌百虫的吸附和选择识别能力，并对其结构进行表征。

The absorption property and selective recognition ability of the imprinted polymer in pure water and additives-water media were studied respectively.

分别考察了印迹柱在纯水以及水中有添加剂存在下的吸附和选择性识别能力。

The extinction of self is salvation; the annihilation of self is the condition of enlightenment; the blotting out of self is Nirvana.

灭绝的自我救赎；的自我毁灭的条件是启蒙；的印迹的自我涅磐。

With western blot analysis and DNA polymerase chain reaction-single strand conformation polymorphism assay,protein product of Rb gene and mutation in exon 5～8 of P_(53) gene were examined in 17 cases of human testicular seminoma.

采用Western印迹和DNA聚合酶链反应－单股构造多态性分析法对17例人睾丸精原细胞瘤组织标本的抗癌基因Rb表达的蛋白产物和P_（53）基因外显子5～8的突变进行检测，发现有3例标本的Rb基因表达的蛋白产物缺失，有4例标本的P_（53）基因有点突变，对照的正常人睾丸组织和视网膜组织均呈Rb基因蛋白产物表达阳性，对照的正常人睾丸组织中未发现P_（53）基因突变。

METHODS: The expression level of HIF-1α and VEGF protein and mRNA were also assayed by western blotting and semiquantitative RT-PCR.

半定量RT-PCR检测HIF-1α、VEGF mRNA的表达，蛋白质印迹法检测HIF-1α和VEGF蛋白的表达。

Western blot was used to measure HSP70 of ischemia and non-ischemia myocardium and the expression of HSP70 was analyzed semiquantitatively.

采用蛋白质免疫印迹法检测各组缺血区和非缺血区心肌组织HSP70含量，并检测血清一氧化氯、丙二醛含量及总超氧化物歧化酶、肌酸激酶活性变化。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。