KCNJ13 产品
(Potassium Inwardly-Rectifying Channel, Subfamily J, Member 13 (KCNJ13))
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This gene encodes a member of the inwardly rectifying potassium channel family of proteins. Members of this family form ion channel pores that allow potassium ions to pass into a cell. The encoded protein belongs to a subfamily of low signal channel conductance proteins that have a low dependence on potassium concentration. Mutations in this gene are associated with snowflake vitreoretinal degeneration. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010].
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Human, Mouse, Rat
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- (2)
Cat. No.
ABIN6262749
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100 μL
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Human
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WB, IHC, IHC (p)
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ABIN1907135
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200 μL
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Human
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ABIN656321
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400 μL
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Latest Publications for our KCNJ13 Products
: "Characterization of the R162W Kir7.1 mutation associated with snowflake vitreoretinopathy." in: American journal of physiology. Cell physiology, Vol. 304, Issue 5, pp. C440-9, (2013) (PubMed).Synonyms and alternative names related to KCNJ13
potassium voltage-gated channel subfamily J member 13 (KCNJ13), potassium inwardly-rectifying channel, subfamily J, member 13 (kcnj13), potassium channel, inwardly rectifying subfamily J, member 13 (kcnj13), potassium inwardly-rectifying channel, subfamily J, member 13 (Kcnj13), potassium voltage-gated channel subfamily J member 13 (Kcnj13), KIR1.4, kir7.1, KIR7.1, Kir7.1, LCA16, SVDProtein level used designations for KCNJ13
- potassium inwardly-rectifying channel, subfamily J, member 13
- inward rectifier potassium channel 13
- jag
- obe
- jaguar
- obelix
- inwardly rectifying potassium channel 7.1
- inward rectifier potassium channel 13-like
- inward rectifier K(+) channel Kir7.1
- potassium channel, inwardly rectifying subfamily J member 13
- inwardly rectifying potassium channel Kir7.1
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