Kir6.2 Antibody - BSA Free

Western Blot: Kir6.2 Antibody - BSA Free [NBP3-46382] - Mouse spleen tissue were subjected to SDS PAGE followed by western blot with (Kir6.2 antibody) at dilution of 1:300

• Reactivity: Hu, Mu, Rt
• Applications: WB, ELISA, ICC/IF
• Clonality: Polyclonal
• Host: Rabbit
• Conjugate: Unconjugated
• Format: BSA Free

Kir6.2 Antibody - BSA Free Summary

• Description: Novus Biologicals Rabbit Kir6.2 Antibody - BSA Free (NBP3-46382) is a polyclonal antibody validated for use in WB, ELISA and ICC/IF. All Novus Biologicals antibodies are covered by our 100% guarantee.
• Immunogen: potassium inwardly-rectifying channel, subfamily J, member 11. (Uniprot# Q14654)
• Isotype: IgG
• Clonality: Polyclonal
• Host: Rabbit
• Gene: KCNJ11
• Purity: Immunogen affinity purified

Applications/Dilutions

• Dilutions:
  • ELISA
  • Immunocytochemistry/ Immunofluorescence 1:20-1:200
  • Western Blot 1:500-1:2000
• Theoretical MW: 48 kDa.
  Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Packaging, Storage & Formulations

• Storage: Store at -20C. Avoid freeze-thaw cycles.
• Buffer: PBS, 50% Glycerol, pH (7.3)
• Preservative: 0.02% Sodium Azide
• Purity: Immunogen affinity purified

Alternate Names for Kir6.2 Antibody - BSA Free

• ATP-sensitive inward rectifier potassium channel 11
• beta-cell inward rectifier subunit
• BIRKIR6.2
• HHF2
• IKATP
• Inward rectifier K(+) channel Kir6.2
• inwardly rectifying potassium channel KIR6.2
• KCNJ11
• Kir6.2
• MGC133230
• PHHI
• potassium channel inwardly rectifing subfamily J member 11
• Potassium channel, inwardly rectifying subfamily J member 11
• potassium inwardly-rectifying channel, subfamily J, member 11
• TNDM3

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. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). [provided by RefSeq]

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Bioinformatics

• Gene Symbol: KCNJ11