產(chǎn)品編號(hào) | bs-23703R |
英文名稱 | ERG/KCNH2 Rabbit pAb |
中文名稱 | 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. |
![]() |
Specific References (1) | bs-23703R has been referenced in 1 publications.
[IF=3.499] Zhan C et al. Rotenone and 3-bromopyruvate toxicity impacts electrical and structural cardiac remodeling in rats. Toxicol Lett. 2019 Oct 1. pii: S0378-4274(19)30295-4. IHC-P ; Rat.
|
研究領(lǐng)域 | 腫瘤 免疫學(xué) 細(xì)胞周期蛋白 通道蛋白 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | Mouse (predicted: Human,Rat,Rabbit,Pig,Sheep,Cow,Dog,Horse) |
產(chǎn)品應(yīng)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 | 127 kDa |
檢測(cè)分子量 | |
細(xì)胞定位 | 細(xì)胞膜 |
性 狀 | Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human ERG/KCNH2: 751-850/1159 <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(xiàng) | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
PubMed | PubMed |
產(chǎn)品介紹 |
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. SWISS: Q12809 Gene ID: 3757 Database links: Entrez Gene: 3757 Human Entrez Gene: 16511 Mouse Omim: 152427 Human SwissProt: Q12809 Human SwissProt: O35219 Mouse Unigene: 647099 Human Unigene: 6539 Mouse Unigene: 10970 Rat |
產(chǎn)品圖片 | |
| 国产成人a亚洲精品无 | yw33777.com尤物| 东北辽女好叫床脏对白 | 国产又爽 又黄 免费 | 国产高潮的无套A片激情视频大全 | 2022精品国偷自产免费观看 | 国产黄在线观看免费观看不卡 | 午夜理理伦电影A片无码新新娇妻 | 在线观看入口黄最新永久免费国产 | 国产精品久久久久久久久久久久无码 | 清纯白嫩初高中在线播放 | 黑人解禁久久影院 | 91福利国产在线观看 | 激情小说中文字幕 | 成人 精品美女隐私漫画 | 国产精品久久久久久高潮 | 欧美日韩中文字幕一区二区 | 国产又爽又粗又猛又色又 | 国产一级a毛一级a看免 | 一区二区三区在线观看免费 | 亚洲激情视频在线观看 | Xiao77熟女精品视频 | 男女午视频免费观看 | 午夜成人国产精品影视 | 日韩精品中文字幕欧美一区二 | 国产精品秘 久久久久久 | 狼人精品A片一区二区 | 真实的国产乱XX熟妇免费 | 91人澡人人爽人人精品 | 亚洲综合成人在线 | 国产高清无码在线 | 西西4ww大尺无码视频 | 中国少妇自慰成人A片 | 国产成人一区二区三区别 | 黄A三级片免费看APP | 成人在线一区二区 | 亚洲一二三区在线观看 | 看高清中文字幕AV福利 | 少妇又黑又粗又大无码A片直播 | 久草精品视频在线观看 |