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GK2 antibody (AA 487-515)

This Rabbit Polyclonal antibody specifically detects GK2 in WB, ELISA and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN3031093

Quick Overview for GK2 antibody (AA 487-515) (ABIN3031093)

Target

See all GK2 Antibodies
GK2 (Glycerol Kinase 2 (GK2))

Reactivity

  • 56
  • 19
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 54
  • 3
Rabbit

Clonality

  • 56
  • 1
Polyclonal

Conjugate

  • 28
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GK2 antibody is un-conjugated

Application

  • 47
  • 18
  • 13
  • 13
  • 13
  • 8
  • 7
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Binding Specificity

    • 15
    • 7
    • 6
    • 5
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 487-515

    Cross-Reactivity (Details)

    Expected species reactivity: Bovine, Primate

    Purification

    Purified

    Immunogen

    A portion of amino acids 487-515 from the human protein was used as the immunogen for this Glycerol kinase 2 antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the Glycerol kinase 2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,IHC (Paraffin): 1:50-1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS pH 7.4 with 0.09 % 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

    Storage Comment

    Aliquot the Glycerol kinase 2 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    GK2 (Glycerol Kinase 2 (GK2))

    Background

    The human glycerol kinase gene family consists of at least 3 expressed loci. The GK1 locus on Xp21.3 is the site of mutations (deletions) causing glycerol kinase deficiency. It comprises 19 exons and is probably ancestral to several other genes which, because they are intronless, are suspected of having arisen by reverse transcriptase mediated events. These include 2 genes on chromosome 4. They are expressed as a single mRNA species in testis where expression is at a high level.

    UniProt

    Q14410
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