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GLYCTK antibody (AA 251-350) (AbBy Fluor® 647)

This anti-GLYCTK antibody is a Rabbit Polyclonal antibody detecting GLYCTK in WB, IF (cc) and IF (p). Suitable for Mouse.
Catalog No. ABIN1698522

Quick Overview for GLYCTK antibody (AA 251-350) (AbBy Fluor® 647) (ABIN1698522)

Target

See all GLYCTK Antibodies
GLYCTK (Glycerate Kinase (GLYCTK))

Reactivity

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  • 34
  • 19
  • 5
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  • 1
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Mouse

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This GLYCTK antibody is conjugated to AbBy Fluor® 647

Application

  • 44
  • 23
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  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Binding Specificity

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    AA 251-350

    Cross-Reactivity

    Mouse

    Predicted Reactivity

    Human,Rat

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human HBEBP2/GLYCTK

    Isotype

    IgG
  • Application Notes

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    GLYCTK (Glycerate Kinase (GLYCTK))

    Alternative Name

    HBEBP2/GLYCTK

    Background

    Synonyms: CG9886 like, GLCTK_HUMAN, Glycerate kinase, Glyctk, GLYCTK1, HBeAg binding protein 2, HBeAg binding protein 4, HBeAg-binding protein 4, HBeAgBP4A, HBEBP2, HBEBP4.

    Background: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.

    Gene ID

    132158
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