来一水AV@lysav|亚洲AV无码片VR一区二区三区 |国产亚洲精久久久久久无码|视色4se成人午夜精品久久

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(zhì)量反饋  人才招聘  關于我們  聯(lián)系我們
久久精品亚洲蜜臀av不卡 |亚洲一区在线曰日韩在线|一个人看的WWW片免费高清中文
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-Kir2.1/BF647 Conjugated antibody (bs-17067R-BF647)
訂購熱線:400-901-9800
訂購郵箱:sales@73327.net
訂購QQ:  400-901-9800
技術支持:techsupport@73327.net
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-17067R-BF647
英文名稱1 Rabbit Anti-Kir2.1/BF647 Conjugated antibody
中文名稱 BF647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 www.73327.net 北京博奧森生物技術有限公司
通過國際質(zhì)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(zhì)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
亚洲一区二区三区av高清| 黑人上司粗大拔不出来电影| 亚洲AV午夜国产精品无码中文字| 无码免费人妻A片AAA毛片一区| 国产婷婷六月在线观看| 日韩国产欧美在线观看视频| 水蜜桃成视频人在线看| 小SAO货叫大声点奶真大| 免费无遮挡禁18污污网站| 国产精品免费福利久久欧| 女人爽到喷水的视频大全| 免费A级作爱片免费观看美国| 精品欧美一区二区三区久久久| 18禁止看爆乳奶头无遮挡| 亚洲人成色77777| 宝宝好涨水快流出来免费视频| 日本三级片在线观看| 性国产SE╳O色欲A片欢迎观看| 成AV免费大片黄在线观看| 无码国产精品一区二区免费式直播 | 国产精品丝袜黑色高跟鞋| 色色资源站av无码321| 国产精品综合精品一区| 国产精品成人一区二区不卡| 欧美熟女丝袜一区二区| 久久精品久久久国产区蓝牛| 妈妈的朋友在线| 女人18片毛片60分钟| 日本午夜福利久久精品| 人妻被按摩师玩弄到潮喷| 久久精品午夜一区二区福利| 性欧美丰满熟妇XXXX性久久久| 少妇高潮惨叫久久久久电影69 | 国产人妖乱国产精品人妖| 午夜成熟看A级毛片| 亚洲国产精品无码成人片久久| 国产盗拍SAP私密按摩视频 | 国产成人无码综合亚洲日韩| 爆乳熟妇乱操| 国产成人精品无码一区二区| 国产99精品久久久久久|