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BPGM antibody

The Rabbit Polyclonal anti-BPGM antibody has been validated for WB, ICC and IF. It is suitable to detect BPGM in samples from Human.
Catalog No. ABIN2856491

Quick Overview for BPGM antibody (ABIN2856491)

Target

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

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This BPGM antibody is un-conjugated

Application

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Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)
  • Cross-Reactivity

    Human, Mouse

    Characteristics

    Rabbit Polyclonal antibody to BPGM (2,3-bisphosphoglycerate mutase)
    BPGM antibody [N1C3]

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human BPGM. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: Mouse spleen , 293T , A431 , H1299

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.84 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

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

    Alternative Name

    bisphosphoglycerate mutase

    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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