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GAPDH antibody (AA 2-335)

This anti-GAPDH antibody is a Mouse Monoclonal antibody detecting GAPDH in WB, ELISA, IHC, IF and IP. Suitable for Human.
Catalog No. ABIN7153642

Quick Overview for GAPDH antibody (AA 2-335) (ABIN7153642)

Target

See all GAPDH Antibodies
GAPDH (Glyceraldehyde-3-Phosphate Dehydrogenase (GAPDH))

Reactivity

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  • 1
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Human

Host

  • 179
  • 105
  • 16
  • 9
  • 4
Mouse

Clonality

  • 193
  • 118
Monoclonal

Conjugate

  • 192
  • 31
  • 18
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  • 3
  • 3
  • 3
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This GAPDH antibody is un-conjugated

Application

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Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP)

Clone

10B4E3
  • Binding Specificity

    • 35
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    • 7
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    • 1
    • 1
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    • 1
    AA 2-335

    Cross-Reactivity

    Human, Mouse, Rabbit

    Purification

    Protein G purified

    Immunogen

    Recombinant Human GAPDH protein (2-335AA)

    Isotype

    IgG1, IgG1 kappa
  • Application Notes

    Recommended dilution: WB: 1:5000-1:80000, IHC: 1:200-1:500, IF: 1:50-1:100, IP: 2 μL-8 μL,

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Preservative: 0.03 % Proclin 300
    Constituents: 50 % Glycerol, 0.01M PBS, PH 7.4

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C,-80 °C

    Storage Comment

    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target

    GAPDH (Glyceraldehyde-3-Phosphate Dehydrogenase (GAPDH))

    Alternative Name

    GAPDH

    Background

    Background: Glyceraldehyde 3-phosphate dehydrogenase (GAPDH or G3PDH) is an enzyme of 37 kDa that is consisdered as a cellular enzyme involved in glycolysis. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a pleiotropic enzyme that is overexpressed in apoptosis and in several human chronic pathologies. Its role as a mediator for cell death has also been highlighted. At the molecular level, sequential steps lead to nuclear translocation of GAPDH during cell death as follows: first, a catalytic cysteine in GAPDH (C150 in rat GAPDH) is S-nitrosylated by nitric oxide (NO) that is generated from inducible nitric oxide synthase (iNOS) and/or neuronal NOS (nNOS), second, the modified GAPDH becomes capable of binding with Siah1, an E3 ubiquitin ligase, and stabilizes it, third, the GAPDH-Siah protein complex translocates to the nucleus, dependent on Siah1's nuclear localization signal, and degrades Siah1's substrates in the nucleus, which results in cytotoxicity. A recent report suggests that GAPDH may be genetically associated with late-onset of Alzheimer's disease.-deprenyl, which has originally been used as a monoamine oxidase inhibitor for Parkinson's disease, binds to GAPDH and displays neuroprotective actions.

    Aliases: GAPDH, G3PD, GAPD, MGC88685

    UniProt

    P04406
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