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PGAM2 antibody (AA 1-253)

This anti-PGAM2 antibody is a Mouse Monoclonal antibody detecting PGAM2 in WB, IF, ELISA and ICC. Suitable for Human.
Catalog No. ABIN5776232

Quick Overview for PGAM2 antibody (AA 1-253) (ABIN5776232)

Target

See all PGAM2 Antibodies
PGAM2 (phosphoglycerate Mutase 2 (Muscle) (PGAM2))

Reactivity

  • 30
  • 21
  • 8
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Human

Host

  • 27
  • 5
  • 2
Mouse

Clonality

  • 29
  • 5
Monoclonal

Conjugate

  • 28
  • 2
  • 1
  • 1
  • 1
  • 1
This PGAM2 antibody is un-conjugated

Application

  • 34
  • 19
  • 11
  • 10
  • 6
  • 6
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
Western Blotting (WB), Immunofluorescence (IF), ELISA, Immunocytochemistry (ICC)

Clone

AT5A7
  • Binding Specificity

    • 8
    • 5
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-253

    Purpose

    Human PGAM2 antibody

    Purification

    Purified

    Immunogen

    Recombinant human PGAM2 (1-253aa) purified from E. coli

    Isotype

    IgG2b kappa
  • Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    Phosphate-Buffered Saline ( pH 7.4) with 0.02 % Sodium Azide, 10 % glycerol

    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

    4 °C,-20 °C,-80 °C

    Storage Comment

    Can be stored at +2C to +8C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
  • Target

    PGAM2 (phosphoglycerate Mutase 2 (Muscle) (PGAM2))

    Alternative Name

    PGAM2

    Background

    Phosphoglycerate mutase (PGAM) catalyzes the reversible reaction of 3-phosphoglycerate (3-PGA) to 2-phosphoglycerate (2-PGA) in the glycolytic pathway. Since both 3-PGA and 2-PGA are allosteric regulators of the pentose phosphate pathway (PPP) and glycine and serine synthesis pathways, respectively, PGAM2 may contribute to the biosynthesis of amino acids, 5-carbon sugar, and nucleotides precursors. The PGAM is a dimeric enzyme containing, in different tissues, different proportions of a slow-migrating muscle (MM) isozyme, a fast-migrating brain (BB) isozyme, and a hybrid form (MB). Mutations in this gene cause muscle phosphoglycerate mutase deficiency, also known as glycogen storage disease X. PGAM2 is one of two PGAM subunits found in humans and is predominantly expressed in adult muscle.

    NCBI Accession

    NP_000281
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