heavy chain的例句大全

Study on Detection of Clonal Immunoglobulin Heavy Chain Gene Rearrangement in Paraffin-embedded Tissues from B-cell Lymphomas

石蜡包埋B细胞性恶性淋巴瘤组织克隆性免疫球蛋白重链基因重排检测研究

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Cloning and sequencing the variable gene from the heavy chain of monoclonal

抗HSV糖蛋白单克隆抗体重链可变区DNA的克隆及序列分析

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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。

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In view of the close relationship betweeen skeletal muscle fiber type, body glucose utilization and development of diabetes, we hypothesized that GLP-1 treatment at early development stage may program skeletal muscle fiber type through regulation of myosin heavy chain expression.

鉴于骨骼肌纤维类型与机体葡萄糖利用和糖尿病发生关系密切，我们假设发育早期GLP-1处理会通过改变肌球蛋白重链表达而改变肌纤维类型，从而程序化地改变成年后肌肉代谢类型。

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An improved procedure of Southern hybridization for testing the Ig heavy chain genes rearrangement

用改进的探针杂交法检测免疫球蛋白重链基因重排

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Objective To study the tissue-restricted expression ability and activity of cardial myosin heavy chain ( cMHC) gene promoter, and to construct a cardiovascular tissue-specific gene expression vector for gene therapy.

目的探讨心肌肌凝蛋白重链（cMHC）基因启动子的心血管组织特异性及其表达活性，构建心血管组织靶向性表达的基因载体。

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These results indicated that the solubility of myofibrillar proteins in low ionic strength medium was improved by the Maillard reaction, and the myosin heavy chain was selectively conjugated with lactose.

结果表明，乳糖与鲢鱼肉Mf发生美拉德反应后生成的肌原纤维乳糖蛋白在低离子强度溶液中的溶解性得到了有效提高，乳糖能有选择性地与肌球蛋白重链相结合。

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[ Results] Of 81 cases with B-NHL 83.95% ( 68/ 81) were positive for clonal gene immunoglobulin heavy chain gene rearrangement. All 36 cases with reactive hyperplasia were multiclonal and all non-lymphoma tissues of 12 cases were IgH negative.

[结果]81例B鄄NHL中68例IgH阳性（阳性率为83.95%），36例反应性增生均为多克隆性，12例非淋巴瘤组织样本结果IgH均为阴性。

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Using the DNA extracted from bone marrow smears which have been stored routinely as a template, polymerase chain reaction ( PCR) was utilized to detect clonal immunoglobulin heavy chain ( IgH) gene rearrangements in multiple myeloma ( MM) and reactive plasmacytosis ( RP).

从常规保存的骨髓涂片抽提DNA为模板，应用聚合酶链反应（PCR）技术检测多发性骨髓瘤（MM）与反应性浆细胞增多症（RP）IgH基因重排方式。

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The N-terminal end of the heavy chain is responsible for binding to specific pre-synaptic neuronal cell receptors and the C-terminal end facilitates internalization.

重链N端能够结合特定胆碱能神经末梢质膜受体，C端主要在内化过程中起作用。

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Objective To make an Achilles tenotomy rat model to observe the change in soleus weight and expression of myosin heavy chain ( MHC) isoform mRNA, and to find some clues for elucidating the mechanisms of soleus disuse.

目的建立大鼠跟腱切断模型，观测并比较跟腱切断与尾部悬吊大鼠比目鱼肌重量与肌球蛋白重链（MHC）异构体mRNA表达的变化，为探讨骨骼肌废用性萎缩的机理提供实验线索。

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The altered gene expression of myosin heavy chain in human atrial fibrillation

心房颤动患者心房组织肌球蛋白重链基因表达的变化

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The effect of moderate exercise training on skeletal muscle myosin heavy chain distribution in chronic heart failure

中度运动锻炼对慢性心力衰竭患者骨骼肌肌球蛋白重链分布的影响

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Methods Total RNA in the metastatic lymph nodes from patients with colorectal cancer was extracted routinely, and reverse transcriptase PCR employed to amplify the heavy chain Fd and light chain κ cDNA.

方法取大肠癌病人转移淋巴结，提取淋巴结总RNA，逆转录PCR扩增重链Fd和K轻链cDNA。

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the molecular weight of heavy chain and light chain of pseudosciaena crocea igm were 76?

大黄鱼免疫球蛋白重链的分子量在76kD左右；

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Basic Study on Fibroin Heavy Chain Gene of Silkworm, Bombyx Mori and It's Application

家蚕丝素重链基因应用的相关基础研究

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cdna sequence analysis of serum immunoglobulin m heavy chain gene of tilapia nilotica

罗非鱼免疫球蛋白（IgM）重链基因全长cDNA序列分析

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METHODS: By using human Tac antigen signal peptide and κ chain and γ 1 heavy chain gene fragments of human Ig, we constructed a versatile expression vector for human mouse chimeric antibody and used it to transfect cultured 293T cells.

方法：用人Tac抗原信号肽以及人IgCκ基因和γ1CH基因，构建人鼠嵌合抗体的表达载体，并转染真核细胞293T进行表达。

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Expression and production of both heavy chain and light chain of human IgG were confirmed by Western blotting analysis.

WESTERN BLOTTING显示上清和细胞内均有人IgG重链和轻链的表达。

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Proteomic analysis indicated that IUGR decreased the expression abundances of shear force-related myosin heavy chain and troponin T, and energy metabolism-related pyruvate kinase and phosphoglycerate mutase ( P0.05).

蛋白质组学分析表明，IUGR减少与肌肉剪切力相关的肌球蛋白重链和肌钙蛋白表达量以及与能量代谢相关的丙酮酸激酶和磷酸甘油变位酶表达量（P0.05）。

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