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Rabbit Anti-ACTHR, Alexa Fluor 750 conjugated antibody (bs-11408R-AF750)
~~~促销,代码KX240301~~~
~~~促销,代码KX240302~~~
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说明书: 100ul  
100ul/2980.00元
大包装/询价
产品编号 bs-11408R-AF750
英文名称 ACTHR, Alexa Fluor 750 conjugated
中文名称 AF750标记的促肾上腺皮质激素受体
别    名 ACTH receptor; ACTH-R; ACTHR; ACTHR_HUMAN; Adrenocorticotropic hormone receptor; Adrenocorticotropin receptor; Corticotropin receptor; MC2 receptor; MC2-R; MC2R; Melanocortin 2 receptor (adrenocorticotropic hormone); Melanocortin 2 receptor; Melanocortin receptor 2.  
研究领域 肿瘤  心血管  细胞生物  神经生物学  信号转导  G蛋白偶联受体  G蛋白信号  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应
产品应用
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 34kDa
细胞定位 细胞膜 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MC2 receptor: 67-105/297 <Extracellular>
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 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.

Function:
Receptor for ACTH. This receptor is mediated by G proteins (G(s)) which activate adenylate cyclase.

Subunit:
Interacts with FALP/MRAP.

Subcellular Location:
Cell membrane; Multi-pass membrane protein.

Tissue Specificity:
Melanocytes and corticoadrenal tissue.

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.

Similarity:
Belongs to the G-protein coupled receptor 1 family.

SWISS:
Q92506

Gene ID:
4158

Database links:

Entrez Gene: 483980 Dog

Entrez Gene: 4158 Human

Entrez Gene: 17200 Mouse

Entrez Gene: 282839 Rat

Omim: 607397 Human

SwissProt: Q01718 Human

SwissProt: Q64326 Mouse

Unigene: 248144 Human

Unigene: 426053 Mouse

Unigene: 92460 Rat



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