97久久久精品综合88久久_亚洲国产精品一_久热热国产久热_97操操操_北条麻妃在线免费观看_精品国自产拍天天拍

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯系我們
最近的中文字幕在线看视频,91精品国产手机,亚洲欧美日本精品
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-GCM2/HRP Conjugated antibody (bs-13314R-HRP)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-13314R-HRP
英文名稱 Rabbit Anti-GCM2/HRP Conjugated antibody
中文名稱 辣根過氧化物酶標記的絨毛膜特異性轉錄因子GCM2抗體
別    名 Chorion-specific transcription factor GCMb; GCM motif protein 2; GCMb; Glial cells missing homolog 2; glial cells missing homolog b; GCM2_HUMAN.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  發育生物學  干細胞  轉錄調節因子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Horse, Rabbit, )
產品應用 WB=1:500-2000 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 57kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GCM2
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
產品介紹 background:
Glial cells missing homolog 2 (GCM2), also known as Chorion-specific transcription factor GCMb, is a 506 amino acid nuclear protein. GCM2 is a transcription factor that acts as an essential regulator of parathyroid development. GCM2 is also thought to mediate the effect of calcium on parathyroid hormone expression and secretion in parathyroid cells. GCM2 contains one N-terminal GCM domain, which has DNA binding activity. Mutations of the gene that encodes GCM2 are associated with hypoparathyroidism, an autosomal recessive condition characterized by hypocalcemia and hyperphosphatemia.

Function:
Gcm2, a mouse ortholog of the Drosophila Glial Cells Missing gene, is expressed in the parathyroid-specific domains in the 3rd pouches from E9.5. The null mutation of Gcm2 causes aparathyroidism in the fetal and adult mouse and has been proposed to be a master regulator for parathyroid development. During Drosophila embryogenesis Gcm2 plays a crucial role in promoting glial cell differentiation.

Subcellular Location:
Nuclear.

DISEASE:
Defects in GCM2 are a cause of familial isolated hypoparathyroidism (FIH) [MIM:146200]; also known as autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. An autosomal recessive form of FIH also exists.

Similarity:
Contains 1 GCM DNA-binding domain.

Database links:

Entrez Gene: 9247 Human

Omim: 603716 Human

SwissProt: O75603 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.kastlife.cn 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
主站蜘蛛池模板: 欧美色欧美亚洲高清在线观看 | 在线观看国产成人av天堂 | 岛国精品资源网站 | 草久久久久 | 国产一区二区三区不卡在线看 | 影院一区二区 | 国产精品96久久久久久又黄又硬 | 国产不卡一二三区 | 一边捏奶头一边高潮视频 | 欧美aaaaaa午夜精品 | 欧美性猛交xxxx免费看野外 | 在线看高清中文字幕一区 | 免费网站看V片在线18禁无码 | 成人一区二区三区在线观看 | 日本不卡一区二区三区 | 五月丁香六月综合AV | 国产精品一区二区免费久久精品 | www.国产91 | 免费AV大片在线观看入口 | 男女作爱在线播放免费网站 | 黄色一级久久 | www国产成人免费观看视频深夜成人网 | 亚洲国产网址 | 成人片免费看 | 无码专区无码专区视频网址 | avtt香蕉久久 | 无码一区二区三区免费 | 人妻无码久久中文字幕专区 | 国产欧美一区二区三区国产幕精品 | 国精品无码一区二区三区在线 | 鲁大师一区影视 | 35岁少妇被23岁小伙征服 | 精品日产一区二区三区手机 | 99精品偷拍视频一区二区三区 | 久热国产视频 | 久久亚洲国产精品五月天婷 | 91久久精品久久国产性色也91 | 亚洲瑟瑟| 国产香蕉青春草原久久 | 一区二区三区四区五区中文字幕 | 67194熟妇在线永久免费观看 |