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GLUD1 antibody

This Rabbit Polyclonal antibody specifically detects GLUD1 in WB and ELISA. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7003577
$142.80
Plus shipping costs $50.00
20 μL
Shipping to: United States
Delivery in 11 to 15 Business Days

Quick Overview for GLUD1 antibody (ABIN7003577)

Target

See all GLUD1 Antibodies
GLUD1 (Glutamate Dehydrogenase 1 (GLUD1))

Reactivity

  • 42
  • 27
  • 25
  • 14
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 51
  • 3
  • 1
Rabbit

Clonality

  • 40
  • 15
Polyclonal

Conjugate

  • 30
  • 6
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GLUD1 antibody is un-conjugated

Application

  • 40
  • 29
  • 21
  • 18
  • 15
  • 12
  • 11
  • 5
  • 4
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Synthetic peptide of human GLUD1

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.48 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    GLUD1 (Glutamate Dehydrogenase 1 (GLUD1))

    Alternative Name

    GLUD1

    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.

    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 61 kDa

    UniProt

    P00367

    Pathways

    Positive Regulation of Peptide Hormone Secretion, Warburg Effect
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