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
少妇荡乳欲伦交换A片欧美,一级a毛片免费观看久久精品,一级婬片A片AAAA毛片A级
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-CLCN2/PE-Cy7 Conjugated antibody (bs-6470R-PE-Cy7)
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-6470R-PE-Cy7
英文名稱 Rabbit Anti-CLCN2/PE-Cy7 Conjugated antibody
中文名稱 PE-Cy7標記的氯離子通道蛋白2抗體
別    名 Chloride Channel 2; Chloride channel protein 2; Chloride channel, voltage sensitive 2; CIC 2; CIC2; ClC-2; CLC2; Clcn2; CLCN2_HUMAN; ECA2; ECA3; EG13; EGI11; EGMA; EJM6; EJM8.  
規(guī)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  神經(jīng)生物學  信號轉導  通道蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,  (predicted: Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, .)
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 99kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CLCN2/CLC-2
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:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport and maintain cellular volume. The genes encoding human CLC-1 through CLC-7 map to chromosomes 7q32, 3q28, 4q32, Xp22.3, Xp11.23-p11.22, 1p36 and 16p13, respectively. CLC1 is highly expressed in skeletal muscle. Mutations in the gene encoding CLC1 lead to myotonia, an inheritable disorder characterized by muscle stiffness and renal salt wasting. CLC2 is highly expressed in the epithelia of several organs including lung, which suggests CLC2 may be a possible therapeutic target for cystic fibrosis. CLC3 expression is particularly abundant in neuronal tissue, while CLC4 expression is evident in skeletal and cardiac muscle as well as brain. Mutations in the gene encoding CLC5 lead to Dent’s disease, a renal disorder characterized by proteinuria and hypercalciuria. CLC6 and CLC7 are broadly expressed in several tissues including testis, kidney, brain and muscle.

Function:
Voltage-gated chloride channel. Chloride channels have several functions including the regulation of cell volume; membrane potential stabilization, signal transduction and transepithelial transport.

Subcellular Location:
Membrane; Multi-pass membrane protein.

Tissue Specificity:
Ubiquitously expressed. Moderately expressed in aortic and coronary vascular smooth muscle cells and expressed at a low level in aortic endothelial cells.

DISEASE:
Defects in CLCN2 are associated with susceptibility to epilepsy, idiopathic generalized type 11 (EIG11) [MIM:607628]. A disorder characterized by recurring generalized seizures in the absence of detectable brain lesions and/or metabolic abnormalities. Generalized seizures arise diffusely and simultaneously from both hemispheres of the brain.
Defects in CLCN2 are associated with juvenile absence epilepsy type 2 (JAE2) [MIM:607628]. JAE is a subtype of idiopathic generalized epilepsy (IGE) characterized by onset occurring around puberty, absence seizures, generalized tonic-clonic seizures (GTCS), GTCS on awakening and myoclonic seizures.
Defects in CLCN2 are associated with juvenile myoclonic epilepsy type 8 (EJM8) [MIM:607628]. A subtype of idiopathic generalized epilepsy. Patients have afebrile seizures only, with onset in adolescence (rather than in childhood) and myoclonic jerks which usually occur after awakening and are triggered by sleep deprivation and fatigue.

Similarity:
Belongs to the chloride channel (TC 2.A.49) family. ClC-2/CLCN2 subfamily.
Contains 2 CBS domains.

Database links:

Entrez Gene: 1181 Human

Entrez Gene: 12724 Mouse

Entrez Gene: 29232 Rat

Omim: 600570 Human

SwissProt: P51788 Human

SwissProt: Q6IPA9 Human

SwissProt: Q9R0A1 Mouse

SwissProt: P35525 Rat

Unigene: 436847 Human

Unigene: 177761 Mouse

Unigene: 11073 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 www.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(wǎng)安備110107000727號
日本成人一区二区三区 | 国产成人三级在线观看 | 西西4444人体艺术视频 | 91久久精品一区二区别 | 亚洲一区二区中文字幕 | 国产乱妇熟妇与子伦HD | 欧美久久精品一级黑人c片 色婷婷综合久久久中文字幕 | 亚洲一区二区三区在线 | 国产午夜精品一区二区 | 欧美农村妇女精品一区二区 | 海角亂倫精品一区二区 | 成人A片潘金莲在线观看九色 | 无码人妻一区二区三区线花季转件 | 免费黃色三級片国产片 | 少妇激情偷人爽爽91嫩草 | 又粗又硬又长又黄的视频 | 欧美熟妇婬乱A片免费 | 红桃成人网站在线观看 | 欧美婬乱片A片AAA毛姪片 | 色视频二区最新视频 | 四川少妇BBB搡BBB爽爽爽视頻 | 国内一区二区三区免费短视频网站 | 国产亚洲欧美一区二区三区義妇 | 蜜桃视频欧美性爱视频 | 国产精品无码久久久久一区二区 | 丝袜秘书一区二区三区四区 | 色窝窝51精品国产人妻消防 | 国产又黄又大又粗的视频 | 欧美丝袜AAAAA片 | 精产品99永久免费网页版 | 无码人妻一区二区三 | 无码中文AV一区二区三巨 | 91拍真实国产伦偷精品 | 日本乱婬一区二区三区 | 毛片A片中文字幕在线视频 91人妻人人做人人爽九色 | 久久精品国产成人AV | 17c在线精品无码入口 | www.17c.com喷水少妇 | 7777人妻精品无码视频 | 第一福利丝瓜AV导航 | 娇喘91丨丨白浆秘 |