亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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  人才招聘  關于我們  聯系我們
99久久精品国产免费,精品人妻人人做人人爽夜夜爽,高清国产av一区二区三区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-ERG/KCNH2/PE-Cy5.5 Conjugated antibody (bs-1815R-PE-Cy5.5)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-1815R-PE-Cy5.5
英文名稱1 Rabbit Anti-ERG/KCNH2/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標記的特異性鉀離子通道蛋白抗體
別    名 ERG; ERG1; H ERG; HERG 1; HERG; HERG1; LQT 2; LQT2; Potassium channel HERG; SQT1; Voltagegated potassium channel, subfamily H, member 2; KCNH2_HUMAN.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  免疫學  細胞周期蛋白  通道蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human, Rat,  (predicted: Mouse, Dog, Pig, Horse, Rabbit, )
產品應用 Flow-Cyt=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 127kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human HERG
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 potassium voltage gated channel, subfamily H (eag related), member 2 (KCNH2) gene encodes a voltage-gated potassium channel which has an important role in cardiac action potential repolarization in the mammalian heart. Mutations in KCNH2 have been shown to cause chromosome 7-linked congenital long QT syndrome, a disorder associated with delayed cardiac repolarization, prolonged electrocardiographic QT intervals, and the development of ventricular arrhythmias. KCNH2 channels are an important target for many drugs, and have emerged as a significant type of cardiac ion channel.Highly expressed in heart and brain.

Function:
Pore-forming (alpha) subunit of voltage-gated inwardly rectifying potassium channel. Channel properties are modulated by cAMP and subunit assembly. Mediates the rapidly activating component of the delayed rectifying potassium current in heart (IKr). Isoform 3 has no channel activity by itself, but modulates channel characteristics when associated with isoform 1.

Subunit:
The potassium channel is probably composed of a homo- or heterotetrameric complex of pore-forming alpha subunits that can associate with modulating beta subunits. Heteromultimer with KCNH6/ERG2 and KCNH7/ERG3. Interacts with ALG10B (By similarity). Heteromultimer with KCNE1 and KCNE2.

Subcellular Location:
Membrane; Multi-pass membrane protein.

Tissue Specificity:
Highly expressed in heart and brain.

Post-translational modifications:
Phosphorylated on serine and threonine residues. Phosphorylation by PKA inhibits ion conduction.

DISEASE:
Defects in KCNH2 are the cause of long QT syndrome type 2 (LQT2) [MIM:613688]. Long QT syndromes are heart disorders characterized by a prolonged QT interval on the ECG and polymorphic ventricular arrhythmias. They cause syncope and sudden death in response to exercise or emotional stress. Deafness is often associated with LQT2.
Defects in KCNH2 are the cause of short QT syndrome type 1 (SQT1) [MIM:609620]. Short QT syndromes are heart disorders characterized by idiopathic persistently and uniformly short QT interval on ECG in the absence of structural heart disease in affected individuals. They cause syncope and sudden death.

Similarity:
Belongs to the potassium channel family. H (Eag) (TC1.A.1.20) subfamily. Kv11.1/KCNH2 sub-subfamily. Contains 1 cyclic nucleotide-binding domain. Contains 1 PAC (PAS-associated C-terminal) domain. Contains 1 PAS (PER-ARNT-SIM) domain.

Database links:

Entrez Gene: 3757 Human

Entrez Gene: 16511 Mouse

Entrez Gene: 117018 Rat

Omim: 152427 Human

SwissProt: Q12809 Human

SwissProt: O35219 Mouse

SwissProt: O08962 Rat

Unigene: 647099 Human

Unigene: 6539 Mouse

Unigene: 10970 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.www.chomd.com.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: 中文字幕一区二区免费视频图片| 阿v网站在线观看蜜臀av| 亚洲中文婷婷48| 亚洲国产成人99精品激情在线app| 色综合久久中文字幕精品1五月天 色综合久久中文字幕有码 - 日韩A片R级无码 专区 | 91精品国产91热久久久久福利_一区二区国| 一级毛片中文字幕内射| 免费看黄区一区二| ass亚洲熟妇毛茸茸|iOcs| 亚洲国产美女精品久久久久黑暗圣经 | 一级毛片视频性奴| 人妻少妇精品中文字幕av-| 德国熟妇ASs性| 无码自拍一区日韩偷拍二区| 国产在线拍揄自揄拍无码全集| 2021国产麻豆剧果冻传媒入口爱情公寓 | 色爽黄1000部免费软件下载双色球一等奖号码 | 视频二区中文字幕91精品推荐| 国产中国男男GayGay视频| 欲色影视天天一区二区三区色香欲日韩AV无码久久 | 丰满人妻熟女aⅴ中文字幕| 亚洲精品无码成人AAA片美女在瘾匿隐处的家庭按摩 | 四虎影视在线视频国产传媒视频| 国产最新进精品视频1区2区3区 | 久久久久久久无码高潮,国产蜜臀AV无码一区二区三区 | 国产亚洲精品国产艳妇短篇 | 免费观看A毛片一区二区不卡| a天堂中文版免费视频| 人妻精品久久久久中文字幕69| 99热门精品一区二区三区无码久久精品91| 无码成人精品区在线观看_在线观看国产免| 国产精品地址免费一呦二呦三呦| 小森林电影高清完整版在线观看| 国产69精品久久久久9999|精品久久久 | 亚洲中文字幕久久精品无码VA一百度| 精品久久人人爽天天玩人人妻_久 精品久久人人做人人爽综合各类色AV | 99久久无色码中文字幕久久 | 亚洲精品无码AV中文永久在线 | 国产精品XXXX喷水欧美| 熟妇13欧美| 中文字幕无码乱人伦剧情介绍|