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KCNK9 (TASK-3) Polyclonal Antibody

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说明书下载
货号: PG3294
货期: 现货
价格: 50μL/960;100μL/1600;200μL/2560
+


靶点: KCNK9
应用: WB,IHC,IF
反应性 : Human,Rat,Mouse
宿主物种 : Rabbit
MW(Observed): 42kD
同种型-Isotype : IgG

隐藏域元素占位

详细信息

推荐稀释比 : WB 1:1000-2000;IHC 1:100-200;IF 1:50-200
组成 : Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
纯化工艺 : The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
储存 : -15°C to -25°C/1 year(Do not lower than -25°C
浓度 : 1 mg/ml
克隆性 : Polyclonal

抗原&靶点信息

特异性 : KCNK9(TASK-3) protein(A239) detects endogenous levels of KCNK9(TASK-3)
基因名称 : KCNK9
蛋白名称 : Potassium channel subfamily K member 9 (Acid-sensitive potassium channel protein TASK-3) (TWIK-related acid-sensitive K(+) channel 3) (Two pore potassium channel KT3.2) (Two pore K(+) channel KT3.2)
别名 : Potassium channel subfamily K member 9;Acid-sensitive potassium channel protein TASK-3;TWIK-related acid-sensitive K;+;channel 3;Two pore potassium channel KT3.2;Two pore K;+;channel KT3.2;

数据库链接:

Organism

基因 ID

SwissProt

Mouse
背景:

This gene encodes a protein that contains multiple transmembrane regions and two pore-forming P domains and functions as a pH-dependent potassium channel. Amplification and overexpression of this gene have been observed in several types of human carcinomas. This gene is imprinted in the brain, with preferential expression from the maternal allele. A mutation in this gene was associated with Birk-Barel mental retardation dysmorphism syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013],

细胞定位 : Cell membrane ; Multi-pass membrane protein .

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