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BPGM antibody

The Rabbit Polyclonal anti-BPGM antibody has been validated for WB, ELISA and IHC. It is suitable to detect BPGM in samples from Human, Mouse and Rat.
Catalog No. ABIN7111094

Quick Overview for BPGM antibody (ABIN7111094)

Target

See all BPGM Antibodies
BPGM (2,3-bisphosphoglycerate Mutase (BPGM))

Reactivity

  • 54
  • 25
  • 19
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 56
  • 1
Rabbit

Clonality

  • 56
  • 1
Polyclonal

Conjugate

  • 30
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  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This BPGM antibody is un-conjugated

Application

  • 51
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  • 14
  • 13
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  • 10
  • 6
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  • 1
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Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Purification

    Immunogen affinity purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    2, 3-bisphosphoglycerate mutase

    Isotype

    IgG
  • Application Notes

    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 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

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    Expiry Date

    12 months
  • Target

    BPGM (2,3-bisphosphoglycerate Mutase (BPGM))

    Alternative Name

    BPGM

    Background

    Synonyms:DPGM Background:2, 3-diphosphoglycerate (2, 3-DPG) is a small molecule found at high concentrations in red blood cells where it binds to and decreases the oxygen affinity of hemoglobin. This gene encodes a multifunctional enzyme that catalyzes 2, 3-DPG synthesis via its synthetase activity, and 2, 3-DPG degradation via its phosphatase activity. The enzyme also has phosphoglycerate phosphomutase activity. Deficiency of this enzyme increases the affinity of cells for oxygen. Mutations in this gene result in hemolytic anemia. Multiple alternatively spliced variants, encoding the same protein, have been identified.

    Molecular Weight

    30 kDa

    Gene ID

    669

    UniProt

    P07738
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