GBE1 (Human) IP-WB Antibody Pair

Catalog # H00002632-PW1

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Size:1 Set
Price: USD $ 607.00
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  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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Immunoprecipitation of GBE1 transfected lysate using rabbit polyclonal anti-GBE1 and Protein A Magnetic Bead (U0007), and immunoblotted with mouse purified polyclonal anti-GBE1.

  • Specification

    Product Description

    This IP-WB antibody pair set comes with one antibody for immunoprecipitation and another to detect the precipitated protein in western blot.

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (91%); Rat (91%)

    Quality Control Testing

    Immunoprecipitation-Western Blot (IP-WB)

    Immunoprecipitation of GBE1 transfected lysate using rabbit polyclonal anti-GBE1 and Protein A Magnetic Bead (U0007), and immunoblotted with mouse purified polyclonal anti-GBE1.

    Supplied Product

    Antibody pair set content:
    1. Antibody pair for IP: rabbit polyclonal anti-GBE1 (300 ul)
    2. Antibody pair for WB: mouse purified polyclonal anti-GBE1 (50 ug)

    Storage Instruction

    Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.

  • Applications

    Immunoprecipitation-Western Blot

  • Gene Info — GBE1

    Entrez GeneID

    2632

    Gene Name

    GBE1

    Gene Alias

    GBE

    Gene Description

    glucan (1,4-alpha-), branching enzyme 1

    Omim ID

    232500 607839

    Gene Ontology

    Hyperlink

    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

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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