亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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  人才招聘  關于我們  聯系我們
欧美日韩国产成人高清视频,亚洲情xo亚洲色xo无码,av潮喷大喷水系列无码
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Connexin 43/Gold Conjugated antibody (bs-0651R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產品編號 bs-0651R-Gold
英文名稱1 Rabbit Anti-Connexin 43/Gold Conjugated antibody
中文名稱 膠體金標記的間隙連接蛋白43抗體
別    名 Connexin 43; connexin43; Connexin43v; Cx 43v; CX43; CX 43; CX-43; DFNB38; Gap junction 43 kDa heart protein;Connexin-43; Gap junction alpha 1 protein; Gap junction protein alpha 1 43kDa (connexin 43); Gap junction protein alpha 1 43kDa; Gap junction protein alpha like; GJA 1; GJA1; GJA-1; GJAL; HGNC:4282; HGNC:8112; Oculodentodigital dysplasia; ODD; ODOD; SDTY3; Syndactyly type III; CXA1_HUMAN.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領域 腫瘤  免疫學  轉錄調節因子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human, Mouse, Rat, Dog,  (predicted: Chicken, Cow, )
產品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 42kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Connexin-43 (211-260aa)
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產品介紹 background:
This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. The encoded protein is the major protein of gap junctions in the heart that are thought to have a crucial role in the synchronized contraction of the heart and in embryonic development. A related intronless pseudogene has been mapped to chromosome 5. Mutations in this gene have been associated with oculodentodigital dysplasia and heart malformations. [provided by RefSeq].

Function:
Gap junction protein that acts as a regulator of bladder capacity. A gap junction consists of a cluster of closely packed pairs of transmembrane channels, the connexons, through which materials of low MW diffuse from one cell to a neighboring cell. May play a critical role in the physiology of hearing by participating in the recycling of potassium to the cochlear endolymph. Negative regulator of bladder functional capacity: acts by enhancing intercellular electrical and chemical transmission, thus sensitizing bladder muscles to cholinergic neural stimuli and causing them to contract.

Subunit:
A connexon is composed of a hexamer of connexins. Interacts (via C-terminus) with TJP1. Interacts (via C-terminus) with SRC (via SH3 domain). Interacts with UBQLN4. Interacts with SGSM3. Interacts with KIAA1432/CIP150. Interacts with CNST and CSNK1D.

Subcellular Location:
Cell membrane; Multi-pass membrane protein. Cell junction, gap junction.

Tissue Specificity:
Expressed in the heart and fetal cochlea.

Post-translational modifications:
Phosphorylated at Ser-368 by PRKCG; phosphorylation induces disassembly of gap junction plaques and inhibition of gap junction activity. Phosphorylation at Ser-325, Ser-328 and Ser-330 by CK1 modulates gap junction assembly.

DISEASE:
Defects in GJA1 are the cause of autosomal dominant oculodentodigital dysplasia (ODDD) [MIM:164200]; also known as oculodentoosseous dysplasia. ODDD is a highly penetrant syndrome presenting with craniofacial (ocular, nasal, dental) and limb dysmorphisms, spastic paraplegia, and neurodegeneration. Craniofacial anomalies tipically include a thin nose with hypoplastic alae nasi, small anteverted nares, prominent columnella, and microcephaly. Brittle nails and hair abnormalities of hypotrichosis and slow growth are present. Ocular defects include microphthalmia, microcornea, cataracts, glaucoma, and optic atrophy. Syndactyly type 3 and conductive deafness can occur in some cases. Cardiac abnormalities are observed in rare instances.

Similarity:
Belongs to the connexin family. Alpha-type (group II) subfamily.

Database links:

Entrez Gene: 2697 Human

Entrez Gene: 14609 Mouse

Entrez Gene: 24392 Rat

Omim: 121014 Human

SwissProt: P17302 Human

SwissProt: P23242 Mouse

SwissProt: P08050 Rat

Unigene: 74471 Human




Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

間隙連接蛋白-43(Gap junction alpha-1 protein; GJA-1; (Vascular smooth muscle connexin-43))是構成細胞間的通道,小分子成份可以借此在細胞間擴散。Connexin-43也是心肌縫隙連接的主要蛋白之一。
此外,星形細胞、成纖維細胞、平滑肌和腎等組織也有表達Connexin 43.
版權所有 2004-2026 www.www.chomd.com.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: 91制片厂(果冻传媒)原档破解101部无水印全集| 久久久久久96Av| 四虎影视库国产精品亚洲电影| 97色在线观看| 亚洲国产高清在线一区二区三区_ 亚洲国产激情一区二区三区| 精品国产一区二区三区AV | 五月天婷婷在线播放大| 亚洲国产成人久久一区二区三区果冻传媒 | 久久亚洲国产成人精品性色,蜜臀久 | 中文字幕一区二区免费视频图片| XXXX中文字幕视频在线| 国产成人18黄网站在线观看软件_第1集 | 午夜精品久久久久久中宇,亚洲一区二区三区无码国产 | 中文人妻无码一区二区三区信息一亚洲 | 奶交app下载| 久久精品国产99精品国产亚洲黄色| 久久国产综合精品五月天喷水汇| 成年妇女观看在线视频| 制服中文字幕一区二区_免费v| 伊人久久精品一区二区三区精品| 亚洲精品无码激情在线视频| 无码精品人妻一区二区三区影院-亚洲色 | 国产午夜三级一区二区三律师| 草莓樱桃丝瓜秋葵榴莲黄瓜大全| 香蕉在线精品视频在线观看2019| 国产无遮挡又黄又爽免费网站网站| 亚洲男人AV天堂精品少妇| 色YEYE香蕉凹凸在线视频 | 国产羞羞视频在线观看免费观看一区| 亚洲中文字幕久久精品无码VA不卡| 亚洲国产专区一区无| 国产免费内射又粗又爽密桃视频!!!! | 色综合久久中文字幕有码 - 日韩A片R级无码 专区| 国内揄拍国内精品野战| mm131亚洲精品第一页| 免费专区一一色哟哟| 一区二区三区四区在线播放91官方网站 | 人妻无码AV一区二区三区网站| 久久99精品久久久久久不卡l中文无码精品 | 成人动作片在线观看| 人妻无码中文字幕按摩番号| 中文字幕无线码一区二区三区永久在线 |