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重组磷酸化细胞内流钾通道蛋白Kir5,1
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。

重组细胞内流钾通道蛋白Kir5.1
Recombinant KCNJ16
基因名:

KCNJ16


产品别名:

BIR9; HKTD; KIR5.1; KCNJ16; potassium inwardly rectifying channel subfamily J member 16; potassium inwardly rectifying channel subfamily J member 16; inward rectifier potassium channel 16; inward rectifier K(+) channel Kir5.1; inward rectifier K+ channel KIR5.1; potassium channel, inwardly rectifying subfamily J member 16; potassium voltage-gated channel subfamily J member 16; 磷酸化细胞内流钾通道蛋白Kir5.1; 细胞内流钾通道蛋白Kir5.1;


背景信息:
The KIR family of potassium channels possess a greater tendency to allow potassium to flow into the cell rather than out of it. Kir4.1, also known as Kir1.2, is highly expressed in brain including glial cells, astrocytes and cortical neurons. Kir4.1 is also expressed in myelin-synthesizing oligodendrocytes and is crucial to myelination in the developing nervous system. The gene encoding human Kir4.1 maps to chromosome 1. Kir4.2, also known as Kir1.3, is expressed in kidney, lung, heart, thymus and thyroid during development. The gene encoding human Kir4.2 maps to chromosome 21 in the Down syndrome chromosome region 1, and Kir4.2 may play a role in the pathogenesis of Down’s syndrome. Kir 5.1 forms functional channels only by coexpression with either Kir4.1 or Kir4.2 in the kidney and pancreas. The gene encoding human Kir5.1 maps to chromosome 17.
 
 
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