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WB analysis of human cerebellum lysate using GTX88616 SUR1 antibody, C-term. Dilution : 0.5microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human cerebellum lysate using GTX88616 SUR1 antibody, C-term. Dilution : 0.5microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human cerebellum lysate using GTX88616 SUR1 antibody, C-term. Dilution : 0.5microg/ml Loading : 35microg protein in RIPA buffer

SUR1 antibody, C-term

GTX88616
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman
TargetABCC8
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Overview

  • Supplier
    GeneTex
  • Product Name
    SUR1 antibody, C-term
  • Delivery Days Customer
    7
  • Application Supplier Note
    WB: 0.5-1.5microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID6833
  • Target name
    ABCC8
  • Target description
    ATP binding cassette subfamily C member 8
  • Target synonyms
    ABC36; ATP-binding cassette sub-family C member 8; ATP-binding cassette transporter sub-family C member 8; ATP-binding cassette, sub-family C (CFTR/MRP), member 8; HHF1; HI; HRINS; MRP8; PHHI; PNDM3; sulfonylurea receptor (hyperinsulinemia); sulfonylurea receptor 1; SUR; SUR1; SUR1delta2; TNDM2
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDQ09428
  • Protein Name
    ATP-binding cassette sub-family C member 8
  • Scientific Description
    The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein functions as a modulator of ATP-sensitive potassium channels and insulin release. Mutations and deficiencies in this protein have been observed in patients with hyperinsulinemic hypoglycemia of infancy, an autosomal recessive disorder of unregulated and high insulin secretion. Mutations have also been associated with non-insulin-dependent diabetes mellitus type II, an autosomal dominant disease of defective insulin secretion. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2013]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203