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Anti-Kir6.2 (KCNJ11) Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Anti-Kir6.2 (KCNJ11) Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Catalog # BOSSBS-2436R-A680
Supplier:  Bioss
Anti-Kir6.2 (KCNJ11) Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Catalog # BOSSBS-2436R-A680
Supplier:  Bioss

Specifications

  • Antibody type:
    Primary
  • Antigen name:
    Kir6.2 (KCNJ11)
  • Clonality:
    Polyclonal
  • Conjugation:
    Alexa Fluor® 680
  • Flow cytometry:
    Yes
  • Host:
    Rabbit
  • ImmunoChemistry:
    Yes
  • ImmunoFluorescence:
    Yes
  • Isotype:
    IgG
  • Reactivity:
    Human,
    Rat,
    Mouse
  • Western blot:
    Yes
  • Epitope:
    301-390/390
  • Form:
    Liquid
  • Gene ID:
    3767
  • Antigen synonyms:
    KCNJ11|TNDM 3|IRK11_HUMAN|Potassium inwardly rectying channel J11|IRK11|IKATP|Kir 6.2|Potassium channel, inwardly rectying subfamily J member 11|TNDM3|HHF 2|ATP sensitive inward rectier potassium channel 11|BIR|Kir6.2|MGC133230|Inwardly rectying potassium channel KIR6.2|IRK 11|HHF2|Beta cell inward rectier subunit|mBIR|Inward rectier K+ channel Kir6.2|PHHI
  • Modification:
    Unmodified
  • Storage buffer:
    Aqueous buffered solution containing 0,01 M TBS (pH 7,4) with 1% BSA, 0,03% Proclin300 and 50% Glycerol
  • Molecular weight:
    43 kDa
  • Storage temperature:
    Store at −20 °C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
  • Concentration:
    1 µg/µl
  • Shipping temperature:
    4 °C
  • Immunogen:
    KLH conjugated synthetic peptide derived from human Kir62
  • Tested applications:
    ICC
  • Purification:
    Purified by Protein A
  • Pack type:
    Vial
  • Pk:
    100 µl

Specifications

About this item

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 characterised 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). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.

Type: Primary
Antigen: Kir6.2 (KCNJ11)
Clonality: Polyclonal
Clone:
Conjugation: ALEXA FLUOR® 680
Public Immunogen Range: 301-390/390
Host: Rabbit
Isotype: IgG
Reactivity: Human; Mouse; Rat