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GLUD1 / GLUD2 (AA 54-553) antibody (HRP)

The Rabbit Polyclonal anti-GLUD1 / GLUD2 antibody is suitable to detect GLUD1 / GLUD2 in samples from Human, Mouse and Rat. It has been validated for ELISA, WB and IHC.
Catalog No. ABIN7993582
$570.00
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 4 to 7 Business Days

Quick Overview for GLUD1 / GLUD2 (AA 54-553) antibody (HRP) (ABIN7993582)

Target

GLUD1 / GLUD2

Reactivity

Human, Mouse, Rat

Host

  • 12
  • 1
Rabbit

Clonality

  • 13
Polyclonal

Conjugate

  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
HRP

Application

  • 11
  • 5
  • 5
  • 4
  • 4
  • 2
  • 1
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 12
    • 1
    AA 54-553

    Purpose

    Anti-GLUD1/2 Antibody HRP Conjugated

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human GLUD1/2 recombinant protein (Position: S54-A553).

    Isotype

    IgG
  • Application Notes

    Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

    Storage

    -20 °C

    Storage Comment

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

    Expiry Date

    12 months
  • Target

    GLUD1 / GLUD2

    Alternative Name

    GLUD1/2

    Background

    Background: This gene encodes glutamate dehydrogenase, which is a mitochondrial matrix enzyme that catalyzes the oxidative deamination of glutamate to alpha-ketoglutarate and ammonia. This enzyme has an important role in regulating amino acid-induced insulin secretion. It is allosterically activated by ADP and inhibited by GTP and ATP. Activating mutations in this gene are a common cause of congenital hyperinsulinism. Alternative splicing of this gene results in multiple transcript variants. The related glutamate dehydrogenase 2 gene on the human X-chromosome originated from this gene via retrotransposition and encodes a soluble form of glutamate dehydrogenase. Related pseudogenes have been identified on chromosomes 10, 18 and X.

    Gene Full Name: glutamate dehydrogenase 1/2

    Gene ID

    2746, 2747

    UniProt

    P00367
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