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Kir4.1 Monoclonal antibody, PBS Only

Kir4.1 Monoclonal Antibody for WB, Indirect ELISA
Cat No. 66931-1-PBS

产品说明书

CloneNo. 2D6A6

宿主/亚型

Mouse / IgG1

种属反应性

human, mouse

应用

WB, Indirect ELISA

KCNJ10, 2D6A6, ATP-dependent inwardly rectifying potassium channel Kir4.1, ATP-sensitive inward rectifier potassium channel 10, BIRK 10

缓冲液配方:  PBS Only
偶联物:  Unconjugated
规格价格库存


产品信息

66931-1-PBS targets Kir4.1 in WB, Indirect ELISA applications and shows reactivity with human, mouse samples.

经测试应用 WB, Indirect ELISA Application Description
经测试反应性 human, mouse
免疫原

CatNo: Ag16785

Product name: Recombinant human KCNJ10 protein

Source: e coli.-derived, PET28a

Tag: 6*His

Domain: 224-426 aa of BC034036

Sequence: ETIRFSQHAVVASHNGKPCLMIRVANMRKSLLIGCQVTGKLLQTHQTKEGENIRLNQVNVTFQVDTASDSPFLILPLTFYHVVDETSPLKDLPLRSGEGDFELVLILSGTVESTSATCQVRTSYLPEEILWGYEFTPAISLSASGKYIADFSLFDQVVKVASPSGLRDSTVRYGDPEKLKLEESLREQAEKEGSALSVRISNV

种属同源性预测
宿主/亚型 Mouse / IgG1
抗体类别 Monoclonal
产品类型 Antibody
全称 potassium inwardly-rectifying channel, subfamily J, member 10
别名 KCNJ10, 2D6A6, ATP-dependent inwardly rectifying potassium channel Kir4.1, ATP-sensitive inward rectifier potassium channel 10, BIRK 10
计算分子量 379 aa, 41 kDa
观测分子量 40 kDa
GenBank蛋白编号BC034036
基因名称 Kir4.1
Gene ID (NCBI) 3766
RRIDAB_2882257
偶联类型 Unconjugated
形式Liquid
纯化方式Protein G purification
UNIPROT IDP78508
储存缓冲液 PBS only, pH 7.3.
储存条件Store at -80°C.
The product is shipped with ice packs. Upon receipt, store it immediately at -80°C

背景介绍

ATP-sensitive inward rectifier potassium channel 10 (KCNJ10, also known as Kir4.1) is an inwardly rectifying K⁺ channel predominantly expressed in glial cells within the central nervous system. In glial cells, Kir4.1 participates in multiple physiological processes, including the maintenance of extracellular K⁺ homeostasis, preservation of astrocyte resting membrane potential, regulation of cell volume, and promotion of glutamate uptake (PMID: 26961251). Kir4.1 can assemble into Kir4.1/Kir5.1 heteromeric channels, which mediate basolateral K⁺ recycling in renal distal tubules. This activity is essential for tubular Na⁺ reabsorption. Pathogenic mutations in Kir4.1 are associated with EAST/SeSAME syndrome, a genetic disorder marked by renal salt wasting (PMID: 24561201; 8995301).

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