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Last updated: 2016/10/23
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GBE1 purified MaxPab mouse polyclonal antibody (B01P)MaxPab

  • Catalog # : H00002632-B01P
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  • Specification
  • Product Description:
  • Mouse polyclonal antibody raised against a full-length human GBE1 protein.
  • Immunogen:
  • GBE1 (AAH12098.1, 1 a.a. ~ 702 a.a) full-length human protein.
  • Sequence:
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Antibody reactive against mammalian transfected lysate.
  • Storage Buffer:
  • In 1x PBS, pH 7.4
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • GBE1 MaxPab polyclonal antibody. Western Blot analysis of GBE1 expression in human liver.
  • PDF DownloadProtocol Download
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • Western Blot analysis of GBE1 expression in transfected 293T cell line (H00002632-T01) by GBE1 MaxPab polyclonal antibody.

    Lane 1: GBE1 transfected lysate(77.22 KDa).
    Lane 2: Non-transfected lysate.
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  • Application Image
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • enlarge
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • enlarge
  • 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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