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PGAM2 antibody

The Mouse Monoclonal anti-PGAM2 antibody is suitable to detect PGAM2 in samples from Human. It has been validated for WB, IHC and IF.
Catalog No. ABIN2728771
$608.40
Plus shipping costs $50.00
0.1 mL
Shipping to: United States
Delivery in 6 to 9 Business Days

Quick Overview for PGAM2 antibody (ABIN2728771)

Target

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

Reactivity

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Human

Host

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Mouse

Clonality

  • 30
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Monoclonal

Conjugate

  • 30
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  • 1
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  • 1
  • 1
This PGAM2 antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Clone

1C11
  • Characteristics

    Homo sapiens phosphoglycerate mutase 2 (muscle) (PGAM2)

    Purification

    Purified from mouse ascites fluids by affinity chromatography

    Immunogen

    Full length human recombinant protein of human PGAM2(NP_000281) produced in HEK293T cell.

    Isotype

    IgG2b
  • Application Notes

    WB 1:2000, IHC 1:150, IF 1:100,

    Comment

    The concentration of the product may vary between diferrent lots.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5-1.0 mg/mL

    Buffer

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

    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
  • 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. 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). This gene encodes muscle-specific PGAM subunit. Mutations in this gene cause muscle phosphoglycerate mutase eficiency, also known as glycogen storage disease X.

    Molecular Weight

    28.6 kDa

    Gene ID

    5224

    NCBI Accession

    NM_000290

    HGNC

    5224
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