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KCNJ13


Official Full Name
potassium inwardly rectifying channel subfamily J member 13
Organism
Homo sapiens
Gene ID
3769
Background
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]
Synonyms
SVD; LCA16; KIR1.4; KIR7.1

Cat.No. Product Name Price
SHH323231 shRNA set against Mouse KCNJ13 (NM_001110227.1) Inquiry
SHH323235 shRNA set against Rat KCNJ13 (NM_053608.2) Inquiry
SHW010305 shRNA set against Danio rerio KCNJ13 (NM_001045549) Inquiry
Cat.No. Product Name Price
CDFG018985 Mouse Kcnj13 cDNA Clone(NM_001110227.1) Inquiry
CDFR013330 Rat Kcnj13 cDNA Clone(NM_053608.2) Inquiry
MiUTR1R-02820 KCNJ13 miRNA 3'UTR clone Inquiry
CDCB171780 Danio rerio KCNJ13 ORF Clone (NM_001045549) Inquiry
CDCB195481 Rabbit KCNJ13 ORF clone (XM_002721434.2) Inquiry
CDCL123073 Human Kcnj13 ORF clone (NM_001110227.1) Inquiry
CDCR380417 Rat Kcnj13 ORF Clone(NM_053608.2) Inquiry
CDCS409003 Human KCNJ13 ORF Clone (BC037290) Inquiry
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