產(chǎn)品編號 | bs-17067R-APC |
英文名稱 | Rabbit Anti-Kir2.1/APC Conjugated antibody |
中文名稱 | APC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(lǐng)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 Omim: 600681 Human SwissProt: P63252 Human SwissProt: P35561 Mouse 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. |
1、抗體溶解方法 | |
2、抗體修復方式 | |
3、常用試劑的配制 | |
4、免疫組化操作步驟 | |
5、免疫組化問題解答 | |
6、Western Blotting 操作步驟 | |
7、Western Blotting 問題解答 | |
8、關(guān)于肽鏈的設(shè)計 | |
9、多肽的溶解與保存 | |
10、酶標抗體效價測定程序 | |
| 蜜桃人妻Ⅴ一v二精品视频 亚洲国产精品久久久久久久 | 91嫩草精品少妇91嫩草影视剧 | 国产又粗又黄又爽又硬的免费视频 | 91亚洲国产成人久久精品麻豆 | 污网站在线免费观看 | 成人亚洲A片V一区二区三区蜜月 | 欧一美一性一交一乱一性一 | 黄色视频网站免费入口 | 黃色毛片三級三級三級免费看 | 国产做受6高潮A片91 | 艳妇荡乳欲伦2中文字幕 | 久久99精品国产自在现线 | 欧美婬片a片aaa毛片直播 | 院影产aA久aA久福利 | 国产老熟妇尿一尿精品播放一区区 | 人妻丰满精品一区二区A片 欧美寡妇性猛交XXX无码 | 91国產乱高潮白浆 | 深夜福利网你懂的性爱视频自拍偷拍 | 91一级A片在线观看 国产男女无套内射网站 | 91人妻人人做人碰人人爽 | 国产最爽乱婬视频播放 | 波多野吉衣一区二区 | 97伦伦午夜电影理伦片 | 久久久久亚洲AV成人人电影绿帽人妻 | 亚洲蜜桃精久久久久久久久久久久 | 国产真实乱婬A片三区高 | 极品少妇BBBBBB毛片日本 | 啊啊啊肏屄白浆操死我 | 免费一级特黄特色大片 | 奶大灬舒服灬又爽灬高潮 | 少妇高潮A片无套内谢 | 美女扒开尿口让男人桶 | 中文字幕高清珍藏版 | 无码人妻aⅴ一区二区三区麻豆 | WWW 黄色视频 COM | 国产一级婬片A片鲁大师 | 国产成人免费视频在线观看 | 免费无码国产v片在线观看视 | 婷婷伊人綜合亞洲綜合網 | 国产熟女真实乱精品视频 |