SKU: WP14361 Categories: ,

ROM-K Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP14361-100
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Product details

Background:

Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. It is activated by internal ATP and probably plays an important role in potassium homeostasis. The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Mutations in this gene have been associated with antenatal Bartter syndrome, which is characterized by salt wasting, hypokalemic alkalosis, hypercalciuria, and low blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008],

Specifications

Size50μL/100μL
TargetROM-K
ReactivityHuman, Mouse, Rat
ApplicationsWB, IHC, IF
MW(Calculated)45kD
MW(Observed)
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000; IHC 1:50-300; IF 1:200-1:1000; / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenThe antiserum was produced against synthesized peptide derived from human ROMK/Kir1.1. AA range:11-60
SpecificityROM-K Polyclonal Antibody detects endogenous levels of ROM-K protein.
Gene NameKCNJ1
Protein NameATP-sensitive inward rectifier potassium channel 1
Other NameKCNJ1; / ROMK1; / ATP-sensitive inward rectifier potassium channel 1; / ATP-regulated potassium channel ROM-K; / Inward rectifier K; / +; / channel Kir1.1; / Potassium channel; / inwardly rectifying subfamily J member 1
SpeciesHuman
Gene ID3758
UniprotP48048,
Species.1Mouse
Gene ID.156379
Uniprot.1O88335,
Species.2Rat
Gene ID.224521
Uniprot.2P35560
Cellular LocalizationCell membrane; Multi-pass membrane protein . Phosphorylation at Ser-44 by SGK1 is necessary for its expression at the cell membrane. .
Tissue ExpressionIn the kidney and pancreatic islets. Lower levels in skeletal muscle, pancreas, spleen, brain, heart and liver.
Signaling_pathway
Research Areas>>Aldosterone-regulated sodium reabsorption; / >>Gastric acid secretion
FunctionDisease:Defects in KCNJ1 are the cause of Bartter syndrome type 2 (BS2) [MIM:241200]; also termed hyperprostanglandin E syndrome 2. BS refers to a group of autosomal recessive disorders characterized by impaired salt reabsorption in the thick ascending loop of Henle with pronounced salt wasting, hypokalemic metabolic alkalosis, and varying degrees of hypercalciuria. BS2 is a life-threatening condition beginning in utero, with marked fetal polyuria that leads to polyhydramnios and premature delivery. Another hallmark of BS2 is a marked hypercalciuria and, as a secondary consequence, the development of nephrocalcinosis and osteopenia.,Function:In the kidney, probably plays a major role in potassium homeostasis. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is regulated by the concentration of extracellular potassium; as external potassium is raised, the voltage range of the channel opening shifts to more positive voltages. The inward rectification is mainly due to the blockage of outward current by internal magnesium. This channel is activated by internal ATP and can be blocked by external barium.,similarity:Belongs to the inward rectifier-type potassium channel family.,tissue specificity:In the kidney and pancreatic islets. Lower levels in skeletal muscle, pancreas, spleen, brain, heart and liver.,
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