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KCNK9 (TASK-3) Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PN5541
产品名称
KCNK9 (TASK-3) Rabbit Polyclonal Antibody
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)
类别
常规抗体
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)
推荐应用
WB
反应种属
Human,Rat,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
51305
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=51305
Human Swissprot No.
Q9NPC2
Human Swissprot Link
http://www.uniprot.org/uniprotkb/Q9NPC2/entry
Mouse Swissprot No.
Q3LS21
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q3LS21
Rat Swissprot No.
Q9ES08
Rat Swissprot Link
http://www.uniprot.org/uniprot/O54941Q9ES08
免疫原
Synthetic Peptide of KCNK9 (TASK-3) AA range: 220-270
特异性
KCNK9(TASK-3) protein(A239) detects endogenous levels of KCNK9(TASK-3)
稀释度
WB 1:1000-2000, IHC 1:100-200. IF 1:50-200
预测分子量
42kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
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],
组织表达
Mainly found in the cerebellum. Also found in adrenal gland, kidney and lung.
细胞定位
Cell membrane ; Multi-pass membrane protein .
功能
disease:Defects in KCNK9 may be the cause of a syndrome of mental retardation, hypotonia, and facial dysmorphism; also known as Birk Barel syndrome.,disease:Overexpressed in a high proportion of breast cancers. May confer resistance to growth factor deprivation and hypoxia, thereby promoting tumor cell survival in poorly oxygenated areas of solid tumors.,function:pH-dependent, voltage-insensitive, background potassium channel protein.,miscellaneous:Inhibited by phorbol 12-myristate 13-acetate (PMA). TASK-3 current is strongly decreased in the presence of an extracellular pH inferior to 7.0.,similarity:Belongs to the two pore domain potassium channel (TC 1.A.1.8) family.,tissue specificity:Mainly found in the cerebellum. Also found in adrenal gland, kidney and lung.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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