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PGK1 antibody

This anti-PGK1 antibody is a Rabbit Monoclonal antibody detecting PGK1 in WB. Suitable for Human.
Catalog No. ABIN6146160

Quick Overview for PGK1 antibody (ABIN6146160)

Target

See all PGK1 Antibodies
PGK1 (Phosphoglycerate Kinase 1 (PGK1))

Reactivity

  • 77
  • 43
  • 23
  • 5
  • 5
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Human

Host

  • 67
  • 12
  • 1
  • 1
Rabbit

Clonality

  • 59
  • 19
Monoclonal

Conjugate

  • 52
  • 6
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This PGK1 antibody is un-conjugated

Application

  • 62
  • 35
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  • 12
  • 9
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  • 2
  • 2
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  • 1
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  • 1
Western Blotting (WB)
  • Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human PGK1

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Comment

    HIGH QUALITY

    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

    PGK1 (Phosphoglycerate Kinase 1 (PGK1))

    Alternative Name

    PGK1

    Background

    The protein encoded by this gene is a glycolytic enzyme that catalyzes the conversion of 1,3-diphosphoglycerate to 3-phosphoglycerate. The encoded protein may also act as a cofactor for polymerase alpha. Additionally, this protein is secreted by tumor cells where it participates in angiogenesis by functioning to reduce disulfide bonds in the serine protease, plasmin, which consequently leads to the release of the tumor blood vessel inhibitor angiostatin. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Deficiency of the enzyme is associated with a wide range of clinical phenotypes hemolytic anemia and neurological impairment. Pseudogenes of this gene have been defined on chromosomes 19, 21 and the X chromosome. [provided by RefSeq, Jan 2014],HEL-S-68p, MIG10, PGKA,Blood,Cancer,Carbohydrate metabolism,Cardiovascular,Endocrine & Metabolism,Signal Transduction,PGK1

    Molecular Weight

    45 kDa

    Gene ID

    5230

    UniProt

    P00558

    Pathways

    Cellular Glucan Metabolic Process
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