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ROM-K (N-17) Antibody: sc-10692

 |  Datasheet
  • goat polyclonal IgG, 200 µg/ml
  • epitope mapping near the N-terminus of ROM-K of human origin
  • recommended for detection of ROM-K isoforms 1-5 human origin by WB, IF and ELISA; also reactive with additional species, including equine
  • blocking peptide, sc-10692 P
 
Additional ROM-K Antibodies ...
 
Ordering Information
Recommended Support Products:
(click button of application of choice)
WB   IF   siRNA  
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human KCNJ1 3758 11q24.3 NM_000220, NM_153764, NM_153765, NM_153766, NM_153767 P48048
600359
 
Set Currency

 Ordering Information
Product NameCatalog #UnitPriceQtyAddFavorites
ROM-K (N-17) sc-10692 200 µg/ml $279
ROM-K (N-17) P sc-10692 P
(peptide)
100 µg/0.5 ml $61
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
ROM-K siRNA (h) sc-42632 10 µM $258
ROM-K (h)-PR sc-42632-PR 10 µM $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
ROM-K shRNA Plasmid (h) sc-42632-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
ROM-K shRNA (h) Lentiviral Particles sc-42632-V 200 µl $625

ROM-K Background Information
ROM-K, an ATP-sensitive inward rectifying K+ channel (also designated KIR1.1), is a member of the Kir family of K+ channels that controls renal K+ secretion. These K+ channels more readily conduct an inward current rather than an outward current and are constituitively open. Inwardly rectifying K+ channels are a complex of four Kir (Kir1-6) subunits. ROM-K is activated by protein kinase A, and its activity is regulated by phosphatidylinositol 4,5-bisphosphate and intracellular pH. Alternative splicing of ROM-K mRNA yields various isoforms which are differentially expressed in nephrons of the mammalian kidney. Mutations in the ROM-K gene are linked to antenatal Bartter syndrome, an autosomal recessive disorder of renal electrolyte transport.