Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

GLUD1 / GLUD2 (AA 54-553) antibody

The Rabbit Polyclonal anti-GLUD1 / GLUD2 antibody (ABIN7875655) specifically detects GLUD1 / GLUD2 in ELISA, WB, IF, FACS and IHC (p). The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN7875655
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for GLUD1 / GLUD2 (AA 54-553) antibody (ABIN7875655)

Target

GLUD1 / GLUD2

Reactivity

Human, Mouse, Rat

Host

  • 1
  • 1
Rabbit

Clonality

  • 2
Polyclonal

Conjugate

  • 2
Un-conjugated

Application

  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
ELISA, Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 1
    • 1
    AA 54-553

    Purpose

    GLUD1/2 Antibody / GDH1/2

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids S54-A553) was used as the immunogen for the GLUD1/2 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the GLUD1/2 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the GLUD1/2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    GLUD1 / GLUD2

    Alternative Name

    GLUD1/2

    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.

    UniProt

    P00367
You are here:
Chat with us!