購(gòu)物車(chē)
幫助
021-54845833/15800441009
中文名稱(chēng)： KCNJ11抗原（重組蛋白）
英文名稱(chēng)： KCNJ11 Antigen (Recombinant Protein)
別 名： BIR; HHF2; PHHI; IKATP; TNDM3; KIR6.2
儲(chǔ) 存： 冷凍（-20℃）
相關(guān)類(lèi)別： 抗原
概 述：
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Fusion protein corresponding to a region derived from 167-390 amino acids of human KCNJ11 |
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Full name: |
potassium inwardly-rectifying channel, subfamily J, member 11 |
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Synonyms: |
BIR; HHF2; PHHI; IKATP; TNDM3; KIR6.2 |
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Swissprot: |
Q14654 |
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Gene Accession: |
BC112358 |
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Purity: |
>85%, as determined by Coomassie blue stained SDS-PAGE |
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Expression system: |
Escherichia coli |
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Tags: |
His tag C-Terminus, GST tag N-Terminus |
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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. |
