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產(chǎn)品名稱：Anti-HERG/KCNH2/ERG抗體,特異性鉀離子通道蛋白抗體歡迎選購
中文名稱：鉀離子通道蛋白EAG1抗體
英文名稱：Anti-KCNH1/EAG1
產(chǎn)品編號(hào)：BYK-2424R
產(chǎn)品別名：EAG1; h eag; Kv10.1; MGC124420; MGC142269; EAG; Ether a go go potassium channel 1; hEAG1; M eag; MGC124419; Potassium voltage gated channel subfamily H （eag related）, member 1; Voltage gated potassium channel subunit Kv10.1; KCNH1_HUMAN.

本公司另供應(yīng)“鉀離子通道蛋白EAG1抗體”的標(biāo)記有：Alexa Fluor 350 Alexa Fluor 488 Alexa Fluor 555 Alexa Fluor 647 AP APC Biotin Cy3 Cy5 Cy5.5 Cy7 FITC Gold HRP PE PE-Cy3 PE-CY5 PE-CY5.5 PE-CY7 RBITC.
產(chǎn)品規(guī)格：100ug/200ug
產(chǎn)品濃度： 1mg/1ml
抗體來源：兔源、鼠源、山羊
克 隆：?jiǎn)慰寺】贵w、多克隆抗體
抗體類型：一抗
性 狀： 凍干粉或液體
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.

Anti-HERG/KCNH2/ERG抗體,特異性鉀離子通道蛋白抗體歡迎選購技術(shù)說明，產(chǎn)品*，由于篇幅原因，更多信息請(qǐng)：

Anti-CTLA-4/CD152（cytotoxic T-lymphocyte associated Anti-gen-4）  淋巴細(xì)胞相關(guān)抗原4/細(xì)胞毒性T細(xì)胞抗原-4抗體
Anti-CT-R（Calcitonin receptor）  降鈣素受體抗體
Anti-CULLIN/Cdc53/CUL/SCFCdc4  CULLIN抗體
Anti-Cx26（Connexin-26）  間隙連接蛋白26抗體
Anti-Cx32（Connexin-32）  間隙連接蛋白32抗體
Anti-CX36 （Connexin-36）  間隙連接蛋白36抗體
Anti-Cx40 （Connexin-40）  間隙連接蛋白40抗體
Anti-Cx43 （Connexin-43）  間隙連接蛋白43抗體
Anti-CX45 （Connexin-45）  間隙連接蛋白45抗體
Anti-CXCR1/IL-8RA （CXC-chemokine receptor 1）  細(xì)胞表面趨化因子受體1抗體
Anti-CXC-R2/CD182（CXC-chemokine receptor 2）  細(xì)胞表面趨化因子受體2抗體
Anti-CXorf36 （uncharacterized protein Cxorf36 precursor）  脫羧酶蛋白體36抗體
Anti-Cyclin A  周期素A抗體
Anti-Cyclin B1  周期素B1抗體
Anti-Cyclin C  周期素C抗體
Anti-Cyclin D1  周期素D1抗體
Anti-Cyclin D2  周期素D2抗體

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.