麻豆av资源_日本三级一区_www.狠狠艹_国产精妇在线观看第一区_成人性生交大片免费看中国A片_日本一本久久

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
天天舔天天干天天操,99在线观看精品,在线观看91精品国产入口
首頁 > 產品中心 > 一抗 > 產品信息
CLCN2 Rabbit pAb (bs-6470R)  
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-6470R
英文名稱 CLCN2 Rabbit pAb
中文名稱 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.  
研究領域 細胞生物  神經生物學  信號轉導  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,Chicken,Dog,Horse)
產品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 99 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 CLCN2/CLC-2: 501-600/898 
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 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.

SWISS:
Q6IPA9

Gene ID:
1181

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



產品圖片
Sample: HepG2 (Human) Cell Lysate at 30 ug Primary: Anti- CLCN2 (bs-6470R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 99 kD Observed band size: 99 kD
版權所有 2004-2026 m.jywcc.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: 午夜精品久久久久久久男人的天堂 | 野花社区www在线观看 | 免费午夜福利不卡片在线 | 四虎成人免费在线 | 无套内谢的新婚少妇国语播放 | 欧美性生活在线观看 | 日本三级网址 | 91啪在线观看 | 91热精品视频 | 欧美1区| 亚洲精品成人久久一区二区 | 男人天堂亚洲成人 | 四虎国产免费 | 欧美激情A∨在线视频播放 se94se亚洲精品setu | 欧美日韩在线观看视频网站 | 成人情趣视频网站 | 青柠高清在线观看免费完整BD | 3344永久在线观看视频免费 | 久久中文字幕在线 | 日本网站一区二区三区 | 国产乱人伦精品一区二区 | 成人午夜sm精品久久久久久久 | 人妻精品久久无码专区涩涩 | 欧美日韩久久久久久 | 日本高清色片 | 男人插女人免费 | 国产三级韩国三级日产三级 | 99热免费| 粉嫩虎白女毛片人体 | 亚洲中文字幕无码MV | 国产70老熟女重口小伙子 | 久久亚洲国产精品亚洲老地址 | 亚洲综合日韩精品欧美综合区 | 国产专区中文字幕 | 狠狠色伊人亚洲综合第8页 日日干天夜夜 | 国内精品伊人久久久久 | 在线黑人抽搐潮喷 | 农村少妇无套内谢粗又长 | 999成人精品 | 日韩一级黄色av | 全亚洲第一av番号网站 |