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GLUD1 antibody

This Rabbit Monoclonal antibody specifically detects GLUD1 in WB, IHC and IF. It exhibits reactivity toward Human.
Catalog No. ABIN7267411

Quick Overview for GLUD1 antibody (ABIN7267411)

Target

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

Reactivity

  • 32
  • 17
  • 17
  • 15
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 41
  • 6
  • 1
Rabbit

Clonality

  • 41
  • 7
Monoclonal

Conjugate

  • 32
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GLUD1 antibody is un-conjugated

Application

  • 34
  • 22
  • 15
  • 13
  • 13
  • 10
  • 6
  • 5
  • 4
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Purpose

    GLUD1 Rabbit mAb

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human GLUD1

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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. [provided by RefSeq, Jan 2016],GDH, GDH1, GLUD,Amino acid metabolism,Cancer,Cell Biology & Developmental Biology,Endocrine & Metabolism,Signal Transduction,GLUD1

    Molecular Weight

    50kDa

    Gene ID

    2746

    UniProt

    P00367

    Pathways

    Positive Regulation of Peptide Hormone Secretion, Warburg Effect
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