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 m.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
国产特黄A片AAAA毛片 | 四川少妇高潮无套毛片 | 一级a免一级a做免费线看内裤游戏 | 国产午夜三级一区二区三 | 日本在线视频免费观看 | 熟女 人妻蜜臀av一区二区三区 | 蜜臀99久久精品久久久久久软件 | 美女裸体洗澡A片免费看 | 成人3D动漫一区二区三区91 | 国产一级片一区二区 | 17C丨国产丨精品入口 | 91精品无码一区二区 | 精品久久久久久久亚洲 | AV老司机午夜免费片 | 躁BBB躁BBB躁BBBBBB | 俄罗斯无码成人午夜电影 | 成人爆乳专区一区二区 | 国产精品色情无码视频A片黑寡妇 | 少妇搡BBBB搡BBB搡爱恋 | 亚洲精品秘 一区二区三区蜜桃久 | 又大又长又粗又硬又黄又爽无遮挡 | 樱桃免费人成网站www | 国产精品久久久久久久久爆乳污 | 亚洲jizz无码人妻 | av高清免费在线观看 | 亂倫國產一級生活片免費 | 成人免费无码区色情免费 | 91精品又黄又爽又舒服 | 波多野结衣亚洲色 | 亚洲国产无码精品 | 伦伦影院午夜理论片痴汉 | 国产视频秘 福利姬在线 | 又大又长又粗一区二区 | 丰满人妻老熟妇伦人精品 | 久久毛片www.17c.com | 国产无套精品一区二区三区 | 中文字幕无码人妻在线视频 | 午夜理理伦一级A片无码软件 | 国产裸体美女视频网站 | 国产色情a v久久无码性 | 午夜成人网站在线观看 |