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  • KCNJ11抗原(重組蛋白)

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    • 品牌 : 通蔚生物
    • 目錄號 : TW17466
    • 應(yīng)用 : 僅供科研使用
    • 保存條件 : 低溫保存
    • 貨期 : 現(xiàn)貨
    • 商品庫存:90
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中文名稱:  KCNJ11抗原(重組蛋白)

英文名稱: KCNJ11 Antigen (Recombinant Protein)

別      名: BIR; HHF2; PHHI; IKATP; TNDM3; KIR6.2

儲      存 冷凍(-20℃)

相關(guān)類別: 抗原

概  述:

Fusion protein corresponding to a region derived from 167-390 amino acids of human KCNJ11


技術(shù)規(guī)格:

Full name:

potassium inwardly-rectifying channel, subfamily J, member 11

Synonyms:

BIR; HHF2; PHHI; IKATP; TNDM3; KIR6.2

Swissprot:

Q14654

Gene Accession:

BC112358

Purity:

>85%, as determined by Coomassie blue stained SDS-PAGE

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

Background:

Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.


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