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Adenylate Kinase 1 antibody (AA 149-189)

This Rabbit Polyclonal antibody specifically detects Adenylate Kinase 1 in WB. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN5647008

Quick Overview for Adenylate Kinase 1 antibody (AA 149-189) (ABIN5647008)

Target

See all Adenylate Kinase 1 (AK1) Antibodies
Adenylate Kinase 1 (AK1)

Reactivity

  • 85
  • 23
  • 17
  • 8
  • 8
  • 8
  • 5
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 81
  • 10
  • 6
Rabbit

Clonality

  • 88
  • 9
Polyclonal

Conjugate

  • 47
  • 10
  • 6
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Adenylate Kinase 1 antibody is un-conjugated

Application

  • 56
  • 35
  • 24
  • 22
  • 13
  • 13
  • 11
  • 10
  • 9
  • 6
  • 6
  • 6
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 17
    • 15
    • 7
    • 7
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 149-189

    Purification

    Antigen affinity purified

    Immunogen

    Amino acids 149-189 (RLETYYKATEPVIAFYEKRGIVRKVNAEGSVDSVFSQVCTH) from the human protein were used as the immunogen for the AK1 antibody.

    Isotype

    IgG
  • Application Notes

    Western blot: 0.5-1 μg/mL

    Restrictions

    For Research Use only
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    -20 °C

    Storage Comment

    After reconstitution, the AK1 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target

    Adenylate Kinase 1 (AK1)

    Alternative Name

    AK1 / Adenylate Kinase 1

    Background

    This gene encodes an adenylate kinase enzyme involved in energy metabolism and homeostasis of cellular adenine nucleotide ratios in different intracellular compartments. This gene is highly expressed in skeletal muscle, brain and erythrocytes. Certain mutations in this gene resulting in a functionally inadequate enzyme are associated with a rare genetic disorder causing nonspherocytic hemolytic anemia. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.

    UniProt

    P00568

    Pathways

    Nucleotide Phosphorylation, Ribonucleoside Biosynthetic Process
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