| 產(chǎn)品編號 | bs-11408R-BF750 |
| 英文名稱(chēng) | ACTHR, BF750 conjugated |
| 中文名稱(chēng) | BF750標記的促腎上腺皮質(zhì)激素受體 |
| 別 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. |
| 研究領(lǐng)域 | 腫瘤 心血管 細胞生物 神經(jīng)生物學(xué) 信號轉導 G蛋白偶聯(lián)受體 G蛋白信號 |
| 抗體來(lái)源 | Rabbit |
| 克隆類(lèi)型 | Polyclonal |
| 交叉反應 | |
| 產(chǎn)品應用 |
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 理論分子量 | 34kDa |
| 細胞定位 | 細胞膜 |
| 性 狀 | Liquid |
| 濃 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human MC2 receptor: 67-105/297 <Extracellular> |
| 亞 型 | IgG |
| 純化方法 | affinity purified by Protein A |
| 緩 沖 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
| 保存條件 | Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. |
| 注意事項 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| PubMed | PubMed |
| 產(chǎn)品介紹 |
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: 4158 Human Entrez Gene: 17200 Mouse Omim: 607397 Human SwissProt: Q01718 Human SwissProt: Q64326 Mouse Unigene: 248144 Human Unigene: 426053 Mouse Unigene: 92460 Rat |
