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KCNJ11 ELISA试剂盒

(Potassium Inwardly-Rectifying Channel, Subfamily J, Member 11 (KCNJ11))

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. [provided by RefSeq, Oct 2009].

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KCNJ11 ELISA 试剂盒 (ABIN1380468)

KCNJ11 适用: 人, 小鼠 pThr224 Colorimetric Cell ELISA Cell Culture Cells

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Popular KCNJ11 ELISA试剂盒

Product

Reactivity

Analytical Method

Validations

Cat. No.

Quantity

Datasheet

KCNJ11 ELISA 试剂盒

Reactivity Human, Mouse

Analytical Method Qualitative Cell ELISA

Validations

Cat. No. ABIN1380468

Quantity 2 x 96 tests

Datasheet Datasheet

Aliases for KCNJ11 ELISA试剂盒

potassium voltage-gated channel subfamily J member 11 (KCNJ11) ELISA试剂盒
potassium inwardly-rectifying channel, subfamily J, member 11 (kcnj11) ELISA试剂盒
potassium inwardly rectifying channel, subfamily J, member 11 (Kcnj11) ELISA试剂盒
potassium voltage-gated channel subfamily J member 11 (Kcnj11) ELISA试剂盒
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