vh

The strain VH was genetically stable and had potential value .

VH遗传性状稳定，是具有潜在应用价值的优良菌株。

The Correct Selection of load in VH Testing

维氏硬度试验负荷的合理选择

The exchange reaction of VH with 001 × 7 was found to be controlled by particle diffusion process .

VH与001×7树脂的交换过程属于粒扩散过程控制。

Construction and expression of the fusion protein consisting of human melanoma specific McAb VH and human TNF

人黑色素瘤单抗VH-TNF融合蛋白基因的构建和表达

Construction and screening of phage display library of VH gene in human anti-Hantaviruses antibody

人源性抗汉坦病毒抗体VH基因噬菌体表面展示文库的构建与筛选

Jejunal mucosal VH and MT in control group were significantly higher than in TPN group .

TPN组空肠粘膜VH、MT明显小于正常组；

But no protein is similar with amino acid sequence encoded by fragment VC and VH .

片段VC、VH未找到与之同源的蛋白质序列。

Then the VH antibodies were selected with PCA using the TP region as the antigen .

以TP区作为抗原，用PCA方法进行VH抗体选择。

When designing the reciprocating vacuum pump , calculating the stroke volume Vh and the max.

一般在设计往复泵时，计算行程容积Vh和最大指示功率Ni时都取相对余隙容积系数λv＝1。

This paper presents a simple basis of Vh for a kind of first order finite element schemes solving three dimensional Navier-Stokes equations .

本文对于一大类数值求解三维k连通区域Ω上的NavierStokes方程（简记为NS方程）边值问题的一阶有限元格式给出零散度空间V~h的一组简单基函数。

The cDNA gene library of VH and VL fragments were amplified by RT-PCR .

设计简并引物，用RT-PCR的方法分别扩增抗体重链和轻链可变区基因cDNA文库。

Conclusion : Results suggest that the method have better stability and easy repetition , and could get higher quantity of VH and VL .

结论：提示该方法具有稳定性好，易于重复，扩增后VH和VL量较高的优点。

RESULTS : The VH and VL genes were homologous with the published gene sequences of mouse antibody variable region .

结果：克隆的基因序列符合小鼠轻、重链可变区基因的特征；

Take the cDNA as a template , the VH and VL gene were amplified by PCR .

以cDNA为模板扩增VH和VL基因片段。

[ Abstract ] Objective To obtain the VH and VL variable region genes of murine McAbs to human CD molecule .

目的获取系列鼠抗人CD分子单抗的轻链及重链可变区基因并进行克隆和测序。

The genes of reshaping anti-CD28 VH that had high antigen binding activity were selected after three round panning selections .

利用PCR产物构建了一个改形抗CD28VH抗体库，经过三轮淘选，获得了具有高结合活性的改形抗体基因。

Biochemistry analysis results showed variation existed between VH and control strain on both zymogram and activity of peroxidase isoenzyme and esterase isoenzyme .

同工酶分析表明：VH过氧化物同工酶，酯酶同工酶谱带数量及酶活性均发生变化；

Methods VH and VL genes of anti-human AFP monoclonal antibody were cloned by RT-PCR from hybridoma .

方法用RT-PCR方法从能分泌特异性抗人AFP单克隆抗体的杂交瘤细胞中分离纯化抗体VH和VL基因。

Cloning and sequencing of the VH / VL genes of anti-CD_4 McAb

抗CD4单克隆抗体可变区基因克隆及测序

In the paper , the homology modelling of Vh and Vl domains of the Fv fragment is reported .

先分别模建了Vh和Vl两个结构域，然后搭建出Fv片段的整体三维结构，并对模建的结构进行了分子力学和动力学优化。

Amplification and Sequencing of Heavy Chain Variable Region ( VH ) Gene of a Human Monoclonal Antibody ( CM-1 ) with Specificity to Breast Cancer

抗乳腺癌人单抗CM-1重链可变区基因的序列测定与分析

The sequence analysis demonstrated that the VL and VH belong to Ig kappa light chain ⅳ subgroup and heavy chain ⅱ subgroup .

序列分析表明所克隆的VL、VH分别属于鼠IgKappa轻链IV亚组和Ig重链亚组。

VH and VL genes of mAb E10 were ligated with human heavy chain CH1 and human CK genes .

将VH基因与人重链恒定区CH1基因连接，VL基因与人CK连接，分别构建了鼠/人嵌合重链FD基因和轻链基因。

The other VH and V κ are functional genes , for they are highly homologous to the variable region genes of murine immunoglobulin .

另一Vκ和VH具备鼠抗体可变区特征，为抗体功能基因。

The antibody contained many protein kinase C phosphorylation sites and casein kinase ⅱ phosphorylation sites in both the VH and VL domains .

VH和VL区均有多个蛋白激酶C磷酸化位点和酪氨酸激酶Ⅱ磷酸化位点。

Our results indicated that the amino acid composition of the FR-1 in heavy chain ( VH ) of antibodies indeed have a great impact on secretion .

可见重链可变区框架Ⅰ区氨基酸的组成对抗体的分泌是有影响的。

Objective To value if the multiple micro-sampling can be used for detecting the ion and element contents in vitreous humor ( VH ) after rabbits died .

目的探讨微量重复取样法对兔玻璃体液样本离子浓度或元素含量检测的可行性。

The critical conditions for the transition between these three penetration modes , i.e. rigid body velocity ( Vr ) and hydrodynamic velocity ( VH ) are determined .

针对这三种状态，确定了临界转化条件即刚体速度（VR）和流体动力学速度（VH）的确定方法。

The VH and VL genes were amplified by RT-PCR , and ScFv was assembled by splicing overlap extension PCR .

RT-PCR扩增出VH和VL基因，经重叠延伸反应组装成单链抗体（ScFv）。

Aim To construct phage display library of VH gene in anti-Hantaviruses ( HV ) antibody and screen humanized anti-HV mAb .

目的构建人抗汉坦病毒（HV）抗体重链可变区（VH）基因噬菌体表面展示文库，筛选人源性抗HV单克隆抗体（mAb）。