脂肪组织特异性低分子量蛋白抗体 MRAP
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仪表展览网>产品库>单克隆抗体
价格: 面议
产品型号:MRAP
公司名称:上海信裕生物技术有限公司
地:上海松江
发布时间:2016-12-01
上海信裕生物技术有限公司
产品简介
脂肪组织特异性低分子量蛋白抗体应用于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免疫抗体。脂肪组织特异性低分子量蛋白抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产品质量,质量稳定,实验效果明显。
产品详情

脂肪组织特异性低分子量蛋白抗体

规格:1mg/1ml

英文名: MRAP

别名: B27; C21orf61; FALP; Fat cell-specific low molecular weight protein; Fat tissue-specific low MW protein; FGD2; GCCD2; Melanocortin-2 receptor accessory protein; Mrap; MRAP_HUMAN.

分子量: 19kDa

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

克隆类型:Polyclonal

亚型:IgG

纯化方法:affinity purified by Protein A

免疫原:KLH conjugated synthetic peptide derived from human MRAP

交叉反应:Human, Mouse, Rat, Rabbit,

细胞定位:细胞浆

脂肪组织特异性低分子量蛋白抗体产品介绍:background: This gene encodes a melanocortin receptor-interacting protein. The encoded protein regulates trafficking and function of the melanocortin 2 receptor in the adrenal gland. The encoded protein can also modulate signaling of other melanocortin receptors. Mutations in this gene have been associated with familial glucocorticoid deficiency type 2. Alternatively spliced transcript variants have been described. [provided by RefSeq, Dec 2009] Function: Required for MC2R expression in certain cell types, suggesting that it is involved in the processing, trafficking or function of MC2R. May be involved in the intracellular trafficking pathways in adipocyte cells. Subcellular Location: Cytoplasm > perinuclear region. Cytoplasm. Cell membrane. Endoplasmic reticulum. Concentrated at the perinuclear membrane region. Upon insulin stimulation, it is redistributed into spotty structures throughout the cytoplasm (By similarity). Localizes both to plasma 脂肪组织特异性低分子量蛋白抗体membrane and endoplasmic reticulum. Tissue Specificity: Expressed in adrenal cortex, testis, breast, thyroid, lymph node, ovary and fat. Expressed in adipose tissues. DISEASE: Defects in MRAP are the cause of glucocorticoid deficiency type 2 (GCCD2) [MIM:607398]; also known as familial glucocorticoid deficiency type 2 (FGD2). GCCD2 is an autosomal recessive disorder due to congenital insensitivity or脂肪组织特异性低分子量蛋白抗体 resistance to adrenocorticotropin (ACTH). It is characterized by progressive primary adrenal insufficiency, without mineralocorticoid deficiency. Similarity: Belongs to the MRAP family. Gene ID: 56246 Database links: Entrez Gene: 56246 Human Omim: 609196 Human SwissProt: Q8TCY5 Human Unigene: 584940 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

脂肪组织特异性低分子量蛋白抗体产品应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=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:肿瘤  心血管  细胞生物  免疫学  信号转导  

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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