MC2-R Polyclonal Antibody

    • 货号:YT2674
    • 应用:WB;ELISA;IHC
    • 种属:Human;Mouse
      • 靶点:
      • MC2-R
      • 简介:
      • >>cAMP signaling pathway;>>Neuroactive ligand-receptor interaction;>>Aldosterone synthesis and secretion;>>Cortisol synthesis and secretion;>>Cushing syndrome
      • 基因名称:
      • MC2R
      • 蛋白名称:
      • Adrenocorticotropic hormone receptor
      • Human Gene Id:
      • 4158
      • Human Swiss Prot No:
      • Q01718
      • Mouse Swiss Prot No:
      • Q64326
      • 免疫原:
      • The antiserum was produced against synthesized peptide derived from human ACTHR. AA range:248-297
      • 特异性:
      • MC2-R Polyclonal Antibody detects endogenous levels of MC2-R protein.
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Polyclonal, Rabbit,IgG
      • 稀释:
      • WB 1:500-2000;IHC 1:50-300; ELISA 2000-20000
      • 纯化工艺:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • 浓度:
      • 1 mg/ml
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 其他名称:
      • MC2R;ACTHR;Adrenocorticotropic hormone receptor;ACTH receptor;ACTH-R;Adrenocorticotropin receptor;Melanocortin receptor 2;MC2-R
      • 实测条带:
      • 34kD
      • 背景:
      • MC2R encodes one member of the five-member G-protein associated melanocortin receptor family. Melanocortins (melanocyte-stimulating hormones and adrenocorticotropic hormone) are peptides derived from pro-opiomelanocortin (POMC). MC2R is selectively activated by adrenocorticotropic hormone, whereas the other four melanocortin receptors recognize a variety of melanocortin ligands. Mutations in MC2R can result in familial glucocorticoid deficiency. Alternate transcript variants have been found for this gene. [provided by RefSeq, May 2014],
      • 功能:
      • disease:Defects in MC2R are the cause of glucocorticoid deficiency type 1 (GCCD1) [MIM:202200]; also known as familial glucocorticoid deficiency type 1 (FGD1). GCCD1 is an autosomal recessive disorder due to congenital insensitivity or resistance to adrenocorticotropin (ACTH). It is characterized by progressive primary adrenal insufficiency, without mineralocorticoid deficiency.,function:Receptor for ACTH. This receptor is mediated by G proteins (G(s)) which activate adenylate cyclase.,similarity:Belongs to the G-protein coupled receptor 1 family.,subunit:Interacts with FALP/MRAP.,tissue specificity:Melanocytes and corticoadrenal tissue.,
      • 细胞定位:
      • Cell membrane; Multi-pass membrane protein.
      • 组织表达:
      • Melanocytes and corticoadrenal tissue.
      • 产品图片
      • Western Blot analysis of various cells using MC2-R Polyclonal Antibody
      • Immunofluorescence analysis of MCF7 cells, using ACTHR Antibody. The picture on the right is blocked with the synthesized peptide.
      • Western blot analysis of lysates from HeLa cells, using ACTHR Antibody. The lane on the right is blocked with the synthesized peptide.
      • Western blot analysis of the lysates from COLO205 cells using ACTHR antibody.
      • Immunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).