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GBE1 antibody (AA 527-556)

The Rabbit Polyclonal anti-GBE1 antibody has been validated for WB and IF. It is suitable to detect GBE1 in samples from Human and Mouse.
Catalog No. ABIN653459

Quick Overview for GBE1 antibody (AA 527-556) (ABIN653459)

Target

See all GBE1 Antibodies
GBE1 (Glucan (1,4-alpha-), Branching Enzyme 1 (GBE1))

Reactivity

  • 49
  • 11
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 40
  • 9
Rabbit

Clonality

  • 43
  • 6
Polyclonal

Conjugate

  • 21
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GBE1 antibody is un-conjugated

Application

  • 40
  • 17
  • 13
  • 13
  • 11
  • 6
  • 6
  • 5
  • 4
  • 4
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (IF)

Clone

RB24029
  • Binding Specificity

    • 15
    • 6
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 527-556

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This GBE1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 527-556 amino acids from the Central region of human GBE1.

    Isotype

    Ig Fraction
  • Application Notes

    IF: 1:10~50. WB: 1:1000. WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

    GBE1 (Glucan (1,4-alpha-), Branching Enzyme 1 (GBE1))

    Alternative Name

    GBE1

    Background

    GBE1 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).

    Molecular Weight

    80474

    Gene ID

    2632

    NCBI Accession

    NP_000149

    UniProt

    Q04446

    Pathways

    Cellular Glucan Metabolic Process
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