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GBE1 293T Cell Transient Overexpression Lysate(Denatured)

  • Catalog # : H00002632-T01
  • Visit Frequency :
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  • Specification
  • Transfected Cell Line:
  • 293T
  • Plasmid:
  • pCMV-GBE1 full-length
  • Host:
  • Human
  • Theoretical MW (kDa):
  • 77.33
  • Quality Control Testing:
  • Transient overexpression cell lysate was tested with Anti-GBE1 antibody (H00002632-B01) by Western Blots.
    SDS-PAGE Gel
    QC Testing of H00002632-T01
    GBE1 transfected lysate.
    Western Blot
    QC Testing of H00002632-T01
    Lane 1: GBE1 transfected lysate ( 77.33 KDa)
    Lane 2: Non-transfected lysate.
  • Storage Buffer:
  • 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
  • Storage Instruction:
  • Store at -80°C. Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Western Blot
  • Application Image
  • Western Blot
  • Gene Information
  • Entrez GeneID:
  • 2632
  • Gene Name:
  • GBE1
  • Gene Alias:
  • GBE
  • Gene Description:
  • glucan (1,4-alpha-), branching enzyme 1
  • Gene Summary:
  • The protein encoded by this gene is a glycogen branching enzyme that catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on the same or a neighboring glycogen chain. Branching of the chains is essential to increase the solubility of the glycogen molecule and, consequently, in reducing the osmotic pressure within cells. Highest level of this enzyme are found in liver and muscle. Mutations in this gene are associated with glycogen storage disease IV (also known as Andersen's disease). [provided by RefSeq
  • Other Designations:
  • amylo-(1,4 to 1,6) transglucosidase,amylo-(1,4 to 1,6) transglycosylase,glycogen branching enzyme,glycogen storage disease type IV
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