Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10)

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Kir4.1; Kir1.2; ATP-sensitive inward rectifier potassium channel 10; ATP-dependent inwardly rectifying potassium channel Kir4.1; Inward rectifier K(+) channel Kir1.2

Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10)
KCNJ10 encodes a member of the inward rectifier-type potassium channel family, characterized by having a greater tendency to allow potassium to flow into, rather than out of, a cell. The encoded protein may form a heterodimer with another potassium channel protein and may be responsible for the potassium buffering action of glial cells in the brain. Mutations in this gene have been associated with seizure susceptibility of common idiopathic generalized epilepsy syndromes.the K(AB)-2/Kir4.1 inwardly rectifying K(+) channel of rat has an ATP-binding domain of Walker-type A motif in the C-terminal intracellular region and is expressed in brain and kidney. In situ hybridization demonstrated that it is expressed predominantly in glial cells of rat membrane but also in the retinal Muller glial cells and marginal cells of the inner ear.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins RPP930Hu01 Recombinant Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10) Positive Control; Immunogen; SDS-PAGE; WB.
Antibodies PAP930Hu01 Polyclonal Antibody to Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10) WB; IHC; ICC; IP.
MAP930Hu21 Monoclonal Antibody to Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10) WB; IHC; ICC; IP.
Assay Kits SEP930Hu ELISA Kit for Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10) Enzyme-linked immunosorbent assay for Antigen Detection.

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10) CLIA Kit Customized Service Offer
n/a ELISA Kit for Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10) Polyclonal Antibody Customized Service Offer
Assay Kits SEP930Ra ELISA Kit for Potassium Inwardly Rectifying Channel Subfamily J, Member 10 (KCNJ10) Enzyme-linked immunosorbent assay for Antigen Detection.
  1. "Cloning and characterization of two K+ inward rectifier (Kir) 1.1 potassium channel homologs from human kidney (Kir1.2 and Kir1.3)."J. Biol. Chem. 272:586-593(1997) [PubMed] [Europe PMC] [Abstract]
  2. "Co-expression of human Kir3 subunits can yield channels with different functional properties."Cell. Signal. 11:871-883(1999) [PubMed] [Europe PMC] [Abstract]
  3. "The DNA sequence and biological annotation of human chromosome 1." Nature 441:315-321(2006) [PubMed] [Europe PMC] [Abstract]
  4. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  5. "Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations." N. Engl. J. Med. 360:1960-1970(2009) [PubMed] [Europe PMC] [Abstract]
  6. "Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10."Proc. Natl. Acad. Sci. U.S.A. 106:5842-5847(2009) [PubMed] [Europe PMC] [Abstract]
  7. "Targeted next generation sequencing as a diagnostic tool in epileptic disorders." Epilepsia 53:1387-1398(2012) [PubMed] [Europe PMC] [Abstract]