强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
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(lián)系我們
人妻体内射精一区二区,haodiaocao,久久婷婷一级婬片A片AAA野外
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Connexin-32/PE-Cy5.5 Conjugated antibody (bs-1376R-PE-Cy5.5)
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-1376R-PE-Cy5.5
英文名稱 Rabbit Anti-Connexin-32/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標記的間隙連接蛋白32抗體
別    名 GJB1; Connexin-32; CX32; Connexin32; Connexin 32; Cx32; CXB1_HUMAN; Charcot Marie Tooth neuropathy X linked; CMTX 1; CMTX1; CX 32; GAP junction 28 kDa liver protein; Gap junction beta 1 protein; Gap junction beta-1 protein; Gap junction protein beta 1 32kD; Gap junction protein beta 1; Gap junction protein beta-1 32kD; GJB 1;CMTX; CMTX1.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 免疫學  神經生物學  通道蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Guinea Pig, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 32kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Connexin-32
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:
Vascular smooth muscle connexin-32 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 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. Mutations in this gene have been associated with oculodentodigital dysplasia and heart malformations.

Function:
One 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.

Subunit:
A connexon is composed of a hexamer of connexins. Interacts with CNST.

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

DISEASE:
Defects in GJB1 are the cause of Charcot-Marie-Tooth disease X-linked type 1 (CMTX1) [MIM:302800]; also designated CMT-X. CMTX1 is a form of Charcot-Marie-Tooth disease, the most common inherited disorder of the peripheral nervous system. Charcot-Marie-Tooth disease is classified in two main groups on the basis of electrophysiologic properties and histopathology: primary peripheral demyelinating neuropathies characterized by severely reduced motor nerve conduction velocities (NCVs) (less than 38m/s) and segmental demyelination and remyelination, and primary peripheral axonal neuropathies characterized by normal or mildly reduced NCVs and chronic axonal degeneration and regeneration on nerve biopsy. CMTX1 has both demyelinating and axonal features. Central nervous system involvement may occur.
Defects in GJB1 may contribute to the phenotype of Dejerine-Sottas syndrome (DSS) [MIM:145900]; also known as Dejerine-Sottas neuropathy (DSN) or hereditary motor and sensory neuropathy III (HMSN3). DSS is a severe degenerating neuropathy of the demyelinating Charcot-Marie-Tooth disease category, with onset by age 2 years. DSS is characterized by motor and sensory neuropathy with very slow nerve conduction velocities, increased cerebrospinal fluid protein concentrations, hypertrophic nerve changes, delayed age of walking as well as areflexia. There are both autosomal dominant and autosomal recessive forms of Dejerine-Sottas syndrome.

Similarity:
Belongs to the connexin family. Beta-type (group I) subfamily.

Database links:

Entrez Gene: 2705 Human

Entrez Gene: 14618 Mouse

Entrez Gene: 29584 Rat

Omim: 304040 Human

SwissProt: O18968 Cow

SwissProt: P08034 Human

SwissProt: P28230 Mouse

SwissProt: P08033 Rat

Unigene: 333303 Human

Unigene: 21198 Mouse

Unigene: 10444 Rat



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 nmgps.com 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(yī)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
国产亚洲综合一区二区 | 麻豆视频在线播放 | 69久蜜桃人妻无码精品一区 | 国产suv精品一区二区 | 久久高清欧美国人妻精品 | 特级西西人体444www高清大 | 四虎成人影视亚洲欧美 | 精品AV伊人大鸡巴 | 无码人妻丰满熟妇一区二区三区 | 久久精品一区二区三区不卡牛牛 | 精品久久久久久久人妻喷密 | 国产精品高潮呻吟久久AV黑人 | 免费 无码 国产在线观看 | 91人妻人人澡人人爽人 | 色情在线观看真人影院 | 成人无码国产一区二区在线观看 | A毛片免费精品一区二区三区 | 爽灬爽灬爽灬毛及A片小说 日韩av无码高清一区免费 | 欧美激情婬妇A片AAA毛多水多 | 少妇BBBBWWw毛视频 | 午夜精品视频久久久男女 | 91无码精品国产 | 蜜乳av蜜汁人妻中文字幕 | Va.日韩人妻在线观看 | 中文字幕在线中文幕免费在线看免费版 | 国产农村妇女毛肩精品Av | 人体一级片在线播放 | 黑人精品xxx一区一二区 | 国产又大又黄的视频 | 亚洲精品一区二区三区中文字幕 | 91人妻一区二区三区蜜臀 | 成人网站在线观看一区 | 特大黑人巨交吊性XXXX视频 | 国产呦小泬泬99精品 | www.毛片.con| 国产无码在线看免费看 | 精品国产免费久久久久久桃子图片 | 亚洲精品国产av | 强伦轩人妻一区二区三区70后 | 国产成人无码精品一区二区 | 粗大猛烈进出灌满白浆一区二区 |