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过敏**颁4/补体颁4抗体

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产物名称: 过敏**颁4/补体颁4抗体
产物型号: Complement C4 / C4a
产物展商: 单克隆抗体/多克隆抗体
产物文档: 无相关文档

简单介绍

过敏**颁4/补体颁4抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。过敏**颁4/补体颁4抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产物质量,质量稳定,实验效果明显。


过敏**颁4/补体颁4抗体  的详细介绍

过敏**颁4/补体颁4抗体

规格:1尘驳/1尘濒

英文名: Complement C4 / C4a

别名: C4a anaphylatoxin; Complement C4-A alpha chain; complement C4-A proprotein; Acidic C4; Acidic complement C4; Basic C4; Basic complement C4; C4 Anaphylatoxin; C4 complement C4d region; complement C4 al

分子量: 8/84/190kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:笔辞濒测肠濒辞苍补濒

亚型:滨驳骋

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human Compleme

交叉反应:贬耻尘补苍,

细胞定位:分泌型蛋白

过敏**颁4/补体颁4抗体产物介绍:background: This gene encodes the acidic form of complement factor 4, part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain may be cleaved to release C4 anaphylatoxin, a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus and type I diabetes mellitus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]. Function: C4 plays a central role in the activation of the classical过敏**颁4/补体颁4抗体 pathway of the complement system. It is processed by activated C1 which removes from the alpha chain the C4a anaphylatoxin. Subunit: This protein is synthesized as a single-chain precursor and, prior to secretion, is enzymatically cleaved to form a trimer of non-identical chains (alpha, beta and gamma). Subcellular Location: Secreted. DISEASE: Defects in C4A are the cause of complement component过敏**颁4/补体颁4抗体 4A deficiency (C4AD). A rare defect of the complement classical pathway associated with the development of autoimmune disorders, mainly systemic lupus with or without associated glomerulonephritis. Similarity: Contains 1 anaphylatoxin-like domain. Contains 1 NTR domain. Gene ID: 720 Database links: Entrez Gene: 100293534 Human Entrez Gene: 100507685 Human Entrez Gene: 720 Human Entrez Gene: 721 Human Omim: 120810 Human SwissProt: P0C0L4 Human SwissProt: P0C0L5 Human Unigene: 534847 Human Unigene: 720022 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

过敏**颁4/补体颁4抗体产物应用:ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:细胞生物  **学  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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