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lambda轻链
相关语句
  light chain constant region
     Cloning and Sequence Analysis of the Bovine Immunoglobulin Lambda Light Chain Constant Region
     牛免疫球蛋白lambda轻链恒定区序列的克隆与研究
短句来源
     The result indicated that there were at least seven C_λ segments in the bovine immunoglobulin lambda light chain constant region.
     这一结果表明牛免疫球蛋白lambda轻链至少含有7个C_λ区,跨越了轻链大小约40kb的范围。
短句来源
     The focus of the dissertation work is to gain some sequence information about the bovine immunoglobulin lambda light chain constant region.
     本研究的主要目的是获得关于牛免疫球蛋白lambda轻链恒定区的序列,为获得敲除免疫球蛋白基因的转基因牛打下基础。
短句来源
  lambda light chain
     There were 31 cas- es of IgG_1—G_4(68.9%),8 IgA_1—A_2(17.8%),2 IgM(4.4%),1 IgD(2.2%)and 3 light chain disease cases. The IgE type was not found and Kappa or Lambda light chain was de- tected in these cases.
     45例多发性骨髓瘤免疫学分型结果:IgG_1—G_4 31例(68.9%)、IgA_1—A_28例(17.8%)、IgM2例(4.4%)、IgD1例(2.2%)、轻链病3例(6.7%),IgE 未检出,45例中都检出有 Kappa 或 lambda 轻链。
短句来源
     The result indicated that there were at least seven C_λ segments in the bovine immunoglobulin lambda light chain constant region.
     这一结果表明牛免疫球蛋白lambda轻链至少含有7个C_λ区,跨越了轻链大小约40kb的范围。
短句来源
     After the patients'sera and urine were mixed with Kappa and Lambda light chain antiserum,human antiserum and IgG,IgA,IgM,IgD,IgE anti-serum,the samples were measured with immuno-electrophoresis,immunoglobulin-detecting and acetate fibre elec- trophoresis.
     本文应用 Kappa、lambda 轻链抗血清和抗全人血清及 IgG、IgA、IgM、IgE 抗血清与患者血清和尿液标本进行免疫电泳,免疫球蛋白测定,醋纤膜电泳。
短句来源
     STUDY ON THE SERUM CONCENTRATIONS OF NEOPTERIN,ICAM 3,KAPPA,LAMBDA LIGHT CHAIN AND KAPPA/LAMBDA RATIO IN SYSTEMIC LUPUS ERYTHEMATOSUS
     SLE血清新喋呤、细胞间粘附分子-3、Kappa、Lambda轻链和轻链比值的研究
短句来源
     Cloning and Sequence Analysis of the Bovine Immunoglobulin Lambda Light Chain Constant Region
     牛免疫球蛋白lambda轻链恒定区序列的克隆与研究
短句来源
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  “lambda轻链”译为未确定词的双语例句
     2. The BAC clone DNA was digested with eight different restriction enzymes and subjected to Southern Blot analysis by hybridization with a 408bp C_λ probe. Seven positive lanes were presented at the most.
     2、为研究lambda轻链C_λ的数量和Igλ的结构,将得到的BAC阳性克隆用不同限制性内切酶酶切,然后与408bp的C_λ区特异性探针杂交,Southern Blot杂交结果显示有7条阳性条带。
短句来源
     Several positive clones containing the bovine C_λ gene segment were isolated from bovine genomic DNA library. About 15kb germline DNA sequence was sequenced.
     通过筛选牛基因组DNA文库,获得含有牛免疫球蛋白lambda轻链的阳性克隆,进而获得免疫球蛋白lambda轻链C区的序列,主要工作包括:
短句来源
     4. Constant region-specific PCR were conducted to investigate how the positive sequences we got arranged using several different primers. The PCR products indicated that the segments S3, S2 and S4 aligned in the lambda light constant region and span about 15kb distance.
     4、利用获得的五个阳性克隆片段的序列,设计六对不同的引物进行PCR扩增,分析扩增产物彼此间的关系,结果表明阳性片段S3,S2和S4依次相邻,分布在牛lambda轻链上15kb的范围内。
短句来源
     Methods:Twenty one cases of FL and the same number cases of RFH were subjected to DNA image cytometry. And bcl 2 protein,Kappa,Lambda light chains were immunohistochemically detected.
     方法 :对 2 1例FL及 2 1例RFH进行bcl 2蛋白、Kappa、Lambda轻链蛋白免疫组化检测及DNA图像细胞分析。
短句来源
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  lambda light chain
Several biochemical parameters, the most important of which are total IgG, kappa and lambda light chain distribution and thin layer isoelectric focusing, were determined in the cerebrospinal fluid of 36 multiple sclerosis patients.
      
Amyloid fibrils were labelled in six of seven cases: in four cases with anti-transthyretin (TTR) antibodies and in two with anti-lambda light chain antibodies.
      
Protein electrophoresis revealed the IgA lambda paraprotein (40.5?g/l) and she had a Bence Jones (BJ) proteinuria of the lambda light chain type.
      
We studied a 58-year-old woman with severe therapy-refractory hyperlipidemia, xanthomatosis, and multiple myeloma (immunoglobulin A, lambda light chain).
      
Evidence for the genomic organization of human lambda light chain joining (J) region gene segments is presented.
      
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After the patients'sera and urine were mixed with Kappa and Lambda light chain antiserum,human antiserum and IgG,IgA,IgM,IgD,IgE anti-serum,the samples were measured with immuno-electrophoresis,immunoglobulin-detecting and acetate fibre elec- trophoresis.Based on the results measured,45 cases with multiple myeloma in our hospital were divided into 5 types——IgG_1—G_4,IgA_1—A_2,IgM,IgD and IgE type.There were 31 cas- es of IgG_1—G_4(68.9%),8 IgA_1—A_2(17.8%),2 IgM(4.4%),1 IgD(2.2%)and 3 light chain disease cases.The...

After the patients'sera and urine were mixed with Kappa and Lambda light chain antiserum,human antiserum and IgG,IgA,IgM,IgD,IgE anti-serum,the samples were measured with immuno-electrophoresis,immunoglobulin-detecting and acetate fibre elec- trophoresis.Based on the results measured,45 cases with multiple myeloma in our hospital were divided into 5 types——IgG_1—G_4,IgA_1—A_2,IgM,IgD and IgE type.There were 31 cas- es of IgG_1—G_4(68.9%),8 IgA_1—A_2(17.8%),2 IgM(4.4%),1 IgD(2.2%)and 3 light chain disease cases.The IgE type was not found and Kappa or Lambda light chain was de- tected in these cases.It was considered that the immunoelectrophoresis was sensitive,simple and correct to group and detect the multiple myeloma,which is suitable for the clinic.

本文应用 Kappa、lambda 轻链抗血清和抗全人血清及 IgG、IgA、IgM、IgE 抗血清与患者血清和尿液标本进行免疫电泳,免疫球蛋白测定,醋纤膜电泳。把多发性骨髓瘤分为:IgG_1—G_1、IgA_1—A_2、IgM、IgD、IgE 型。45例多发性骨髓瘤免疫学分型结果:IgG_1—G_4 31例(68.9%)、IgA_1—A_28例(17.8%)、IgM2例(4.4%)、IgD1例(2.2%)、轻链病3例(6.7%),IgE 未检出,45例中都检出有 Kappa 或 lambda 轻链。免疫电泳对多发性骨髓瘤的检测及分型,具有敏感、准确、简便,适用于临床的优点。

PURPOSE Studies of β- trace have been limited partly by the inability to purify it in sufficient quantities.The main difficulty in purification of β- trace protein is that separated β- trace is always mixed with Kappa andLambda light chain of IgG. This paper describes a procedur of purification of very pure β - trace.MEthODS The procedure mainly consists of two successive fractionations on Sephadex G75 andSephadex G150 and an affinity chromatography with protein G- Sepharose 4 Fast Flow.RESULTS An affinity chromatography...

PURPOSE Studies of β- trace have been limited partly by the inability to purify it in sufficient quantities.The main difficulty in purification of β- trace protein is that separated β- trace is always mixed with Kappa andLambda light chain of IgG. This paper describes a procedur of purification of very pure β - trace.MEthODS The procedure mainly consists of two successive fractionations on Sephadex G75 andSephadex G150 and an affinity chromatography with protein G- Sepharose 4 Fast Flow.RESULTS An affinity chromatography with Protein G - Sepharose 4 Fast Flow can be eliminated in lightchains of IgG and very pure β- trace was purified.CONCLUSIONS This paper describes new procedure of purification of very pure β - trace.

β-微量蛋白(β-trace)是存在于脑脊液(CSF)中的一种微量蛋白,其功能和来源尚未明了。主要问题是其纯化问题未解决。β-微量蛋白经常与IgG的Kappa和lambda轻链混杂,纯化时很难将它们分开。本研究用SephadexG75及SephadexG150柱层析,结合ProteinG-Sepharose4FastFlow亲和层析,去除IgG轻链,得到纯粹的β-微量蛋白。

Aim:To Recognize primary gastrointestinal malignant lymphoma (PMLGI)arsing from mucosa associated lymphoi Tissue (MALT) and to reduce the rates of misdiagnosis and missed diagnosis.Methods: The pathological sections of 32 cases of PMLG were stained with hematoxylin and eosin.Some of them were added Foot,MGP,PAS stain and were studied by immunoenzyme labelling methods,such as Kappa light chain,Lambda light chain,EMA,Keratin and CEA.Results: The lesions often remained locolized in gastrointestine.The tumours...

Aim:To Recognize primary gastrointestinal malignant lymphoma (PMLGI)arsing from mucosa associated lymphoi Tissue (MALT) and to reduce the rates of misdiagnosis and missed diagnosis.Methods: The pathological sections of 32 cases of PMLG were stained with hematoxylin and eosin.Some of them were added Foot,MGP,PAS stain and were studied by immunoenzyme labelling methods,such as Kappa light chain,Lambda light chain,EMA,Keratin and CEA.Results: The lesions often remained locolized in gastrointestine.The tumours consisted of centrocyte-like cells,frequently accompanying with lymphoepithelial lesions and residual germinal centers.Conclusion: The above described pathological changes and immunohistochemistry changes are helpful to the diagnosis of PMLGI.

目的:提高对胃肠粘膜淋巴组织起源的恶性淋巴瘤的认识,以减少误诊、漏诊。方法:32例胃肠道恶性淋巴瘤标本、HE染色、部分附加Foot、MGP、PAS、免疫标记Kappy、Lambda轻链、EMA、Keratin和CEA。结果:病灶多局限于胃肠道,形态学由中心细胞样细胞组成,常伴有淋巴上皮损害及残存滤泡。结论:以上病变和免疫组化有助于诊断胃肠道原发性恶性淋巴瘤

 
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