91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
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
无码人妻一区二区三区免费九色,四川少妇BBw搡BBBB槡BBBB,99成人 国产精品视频
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-Kir2.1/PE-Cy5.5 Conjugated antibody (bs-17067R-PE-Cy5.5)
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(chǎn)品編號 bs-17067R-PE-Cy5.5
英文名稱 Rabbit Anti-Kir2.1/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標記的鉀離子通道Kir2.1抗體
別    名 Cardiac inward rectifier potassium channel; HHBIRK 1; HHBIRK1; HHIRK1; HIRK 1; hIRK1; Inward rectifier K; inwardly rectifying subfamily J member 2; IRK 1; IRK2_HUMAN; IRK1; KCNJ2; KIR2.1; LQT7; Potassium channel; Potassium channel inwardly rectifying subfamily J member 2; Potassium inwardly rectifying channel J2; Potassium inwardly rectifying channel subfamily J member 2; SQT 3; SQT3.  
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  通道蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse, Rat,  (predicted: Human, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
產(chǎn)品應用 Flow-Cyt=1:50-200 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 48kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Kir2.1
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(chǎn)品介紹 background:
Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features. [provided by RefSeq, Jul 2008]

Function:
Probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is regulated by the concentration of extracellular potassium; as external potassium is raised, the voltage range of the channel opening shifts to more positive voltages. The inward rectification is mainly due to the blockage of outward current by internal magnesium. Can be blocked by extracellular barium or cesium.

Subcellular Location:
Membrane.

Tissue Specificity:
Heart, brain, placenta, lung, skeletal muscle, and kidney. Diffusely distributed throughout the brain.

DISEASE:
Defects in KCNJ2 are the cause of long QT syndrome type 7 (LQT7) [MIM:170390]; also called Andersen syndrome or Andersen cardiodysrhythmic periodic paralysis. 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 excercise or emotional stress. LQT7 manifests itself as a clinical triad consisting of potassium-sensitive periodic paralysis, ventricular ectopy and dysmorphic features.
Defects in KCNJ2 are the cause of short QT syndrome type 3 (SQT3) [MIM:609622]. 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. SQT3 has a unique ECG phenotype characterized by asymmetrical T waves.

Similarity:
Belongs to the inward rectifier-type potassium channel (TC 1.A.2.1) family.
KCNJ2 subfamily.

Database links:

Entrez Gene: 3759 Human

Entrez Gene: 16518 Mouse

Entrez Gene: 29712 Rat

Omim: 600681 Human

SwissProt: P63252 Human

SwissProt: P35561 Mouse

SwissProt: Q64273 Rat

Unigene: 1547 Human

Unigene: 4951 Mouse

Unigene: 44415 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 m.rvdoil.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
精品人妻一区二区三区四区色欲 | 欧美××××黑人××性爽 | 国产精品自偷自拍啪啪啪 | 成人免费视频 视频 | 后进极品白嫩翘臀在线视频 | 羞答答免费区国精产品 | 精品人妻无码一区二区性色 | XXXX性XXXXu公交车 | 国产毛片毛片毛片毛片 | 无码精品AV久久久奶水小说 | 91精品人妻一区二区三区蜜桃 | 久久久国产精品一区二区白洁老师 | 免费无码婬AAAA片 | 亚洲一区二区三区在线 | 亚洲精品无码久久久久久久久久久久久 | JIZZ国产精品酒在线观看 | 午夜传媒一区二区三区 | 亚洲AV色香蕉一区二区三区老师 | 欧美黄网站在线免费播放 | 精品人妻一区二区三区线国色天 | 日韩精品中文字幕欧美一区二 | 91麻豆精品A片国产在线观看 | 国产有大有粗有黄的视频 | 国产 成年妇 视频下载 | 人妻日韩精品中文字幕 | 91 无码 真人 中文字幕 | 成人亚洲A片V一区二区三区蜜月 | 天天婬欲婬香婬色婬动态 | 久久国产视频限制免费 | 亚欧精品无码7777视频 | 国产农村妇女毛肩精品Av | 影音先锋成人AV资源 | 中文字幕高清在线观看 | 国内一级一片内射免费 | 北京熟妇槡BBBB槡BBBB | 亂倫近親相姦中文字幕 | 麻豆秘 在线观看国产 | 91精品人妻无码 | 国产一级a毛一级a看免费视频野外 | 九一免费无码高清视频 | 西西44WWW无码免费视频软件 |