Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8)

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Kir6.1; uKATP-1; ATP-sensitive inward rectifier potassium channel 8; Inward rectifier K(+) channel Kir6.1

Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8)
Inagaki et al. (1995) isolated a cDNA from a rat pancreatic islet cell library that encodes a member of the inward rectifier potassium channel family. The predicted 424-amino acid protein, which they designated uKATP-1, has 2 transmembrane domains and shares 43 to 46% identity with other inward rectifier potassium channels, including ROMK1, IRK1, GIRK1, and cKATP-1. When the protein was expressed in Xenopus oocytes, a weak rectifier activity was demonstrated that was blocked with Ba(+2) and activated by diazoxide. Northern blots showed that the mRNA is widely expressed in various tissues of the rat. Inagaki et al. (1995) cloned the human gene, designated KCNJ8. The predicted human protein is 98% identical to that of the rat.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) CLIA Kit Customized Service Offer
n/a ELISA Kit for Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) CLIA Kit Customized Service Offer
n/a ELISA Kit for Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) 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 8 (KCNJ8) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) CLIA Kit Customized Service Offer
n/a ELISA Kit for Potassium Inwardly Rectifying Channel Subfamily J, Member 8 (KCNJ8) ELISA Kit Customized Service Offer
  1. "cDNA sequence, gene structure, and chromosomal localization of the human ATP-sensitive potassium channel, uKATP-1, gene (KCNJ8)."Genomics 30:102-104(1995) [PubMed] [Europe PMC] [Abstract]
  2. "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]
  3. "Genomic organization and expression of KCNJ8/Kir6.1, a gene encoding a subunit of an ATP-sensitive potassium channel."Gene 211:71-78(1998) [PubMed] [Europe PMC] [Abstract]
  4. "J wave syndromes."Heart Rhythm 7:549-558(2010) [PubMed] [Europe PMC] [Abstract]
  5. "Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromes."Heart Rhythm 7:1466-1471(2010) [PubMed] [Europe PMC] [Abstract]
  6. "Loss-of-function mutations in the KCNJ8-encoded Kir6.1 KATP channel and sudden infant death syndrome."Circ. Cardiovasc. Genet. 4:510-515(2011) [PubMed] [Europe PMC] [Abstract]