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GLUD2 antibody (PE-Cy7)

This anti-GLUD2 antibody is a Rabbit Polyclonal antibody detecting GLUD2 in WB. Suitable for Human, Mouse, Rat, Cow and Dog.
Catalog No. ABIN1713285

Quick Overview for GLUD2 antibody (PE-Cy7) (ABIN1713285)

Target

See all GLUD2 Antibodies
GLUD2 (Glutamate Dehydrogenase 2 (GLUD2))

Reactivity

  • 48
  • 7
  • 7
  • 3
  • 3
  • 1
  • 1
  • 1
Human, Mouse, Rat, Cow, Dog

Host

  • 44
  • 4
Rabbit

Clonality

  • 47
  • 1
Polyclonal

Conjugate

  • 20
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GLUD2 antibody is conjugated to PE-Cy7

Application

  • 42
  • 15
  • 13
  • 13
  • 7
  • 6
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Predicted Reactivity

    Human,Mouse,Rat,Dog,Cow,Sheep,Horse,Rabbit

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human GLUD2

    Isotype

    IgG
  • Application Notes

    FCM(1:100-500)
    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    GLUD2 (Glutamate Dehydrogenase 2 (GLUD2))

    Alternative Name

    GLUD2

    Background

    Synonyms: GDH 2, GDH, GDH2, GLUDP1, Glutamate dehydrogenase 2, Glutamate dehydrogenase 2 mitochondrial, Glutamate dehydrogenase pseudogene 1.

    Background: GLUD2 is both mitochondrial matrix enzymes belonging to the Glu/Leu/Phe/Val dehydrogenases family. Exisiting as homohexamers, GLUD1 catalyzes the oxidative deamination of glutamate to ?ketoglutarate and ammonia while GLUD2 is involved in the recycling of glutamate during neurotransmission. GLUD1 is critical for regulating amino acid induced insulin secretion and is allosterically activated by ADP and inhibited by GTP and ATP. Mutations in the gene encoding GLUD1 causes hyperinsulinism-hyperammonemia syndrome (HHS), which is an inherited condition characterized by high insulin and ammonia levels in the blood. GLUD1 may also be involved in learning and memory reactions by increasing the turnover of the excitatory neurotransmitter glutamate. GLUD2 is expressed in testis and retina, with lower levels found in brain.

    Gene ID

    2747

    Pathways

    Synaptic Membrane
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