超碰97自拍_久久99久久98精品免观看软件_在线亚洲一区_九九视频这里只有精品_国产精品一区二区欧美视频_精品国产区一区

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
人妻少妇无码中文幕久久,亚洲一区二区不卡在线观看,97人妻免费碰视频碰免
首頁 > 產品中心 > 一抗 > 產品信息
Connexin-32 Rabbit pAb (bs-1376R)  
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
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價

產品編號 bs-1376R
英文名稱 Connexin-32 Rabbit pAb
中文名稱 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.  
Specific References  (2)     |     bs-1376R has been referenced in 2 publications.
[IF=3.3] Zhang et al. Hydrogen-rich water protects against acetaminophen-induced hepatotoxicity in mice. (2015) World.J.Gastroenterol. 21:4195-209  IHC ;  Mouse.  
[IF=2.43] Zhang, Jing-Yao, et al. "Hydrogen-rich water protects against acetaminophen-induced hepatotoxicity in mice." World Journal of Gastroenterology 21.14 (2015): 4195-4209.  IHC-P ;  Mouse.  
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
克 隆 號
交叉反應 Human (predicted: Mouse,Rat,Rabbit,Pig,Cow,Dog,GuineaPig,Horse)
產品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 32 kDa
檢測分子量
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Connexin-32: 201-283/283 <Cytoplasmic>
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ 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
產品介紹 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.

SWISS:
P08034

Gene ID:
2705

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



產品圖片
Tissue/cell: human cervical carcinoma; 4% Paraformaldehyde-fixed and paraffin-embedded; Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min; Incubation: Anti-Connexin-32 Polyclonal Antibody, Unconjugated(bs-1376R) 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
版權所有 2004-2026 www.ggggww.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: 无码乱人伦一区二区亚洲 | 国产日本亚洲香蕉视频 | 99精品视频免费热播在线观看 | 久热爱精品视频线路一 | 99热免费 | 免费精品一区二区三区第35 | 日本添下边无码视频全过程 | 美日韩一区二区三区 | 人与禽性视频77777交片 | 亚洲精品成人AA片在线播 | 国产骚妻| gay男同帅哥网站在线观看 | 91豆花视频 | 人人揉人人捏人人爽五月天 | 韩国黄色精品 | 国产精选第一页 | 欧美性猛交xxxx偷拍洗澡 | 无码永久成人免费视频 | 一本岛在线视频 | 欧美日韩黄视频 | 中文日韩在线视频 | 正在播放一区二区 | 久久久www成人免费无遮挡大片 | 高清在线观看av | 剑来在线观看免费动漫 | 亚洲精品一区二区三区白峰美 | 欧美狠狠爱 | 亚洲色图手机在线 | 男生戳美女两腿中间那个视频 | 老人把我添到了高潮A片 | 国产91丝袜香蕉在线播放 | 狠狠色狠狠色综合日日32 | 久久精品爱看无码免费视频 | 久久亚洲色WWW成人欧美 | 老女人性生交大片免费 | 日韩中文字幕在线视频观看 | 神马午夜伦理 | 国产综合视频一区二区三区 | 久久国产中文娱乐网 | 怡春院性无码免费视频 | 4438xx亚洲最大五色丁香 |