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ADA antibody (AA 287-314)

This Mouse Monoclonal antibody specifically detects ADA in WB and ELISA. It exhibits reactivity toward Human.
Catalog No. ABIN3029872

Quick Overview for ADA antibody (AA 287-314) (ABIN3029872)

Target

See all ADA Antibodies
ADA (Adenosine Deaminase (ADA))

Reactivity

  • 65
  • 35
  • 19
  • 14
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 76
  • 19
  • 1
Mouse

Clonality

  • 78
  • 18
Monoclonal

Conjugate

  • 52
  • 8
  • 6
  • 6
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ADA antibody is un-conjugated

Application

  • 85
  • 41
  • 15
  • 15
  • 13
  • 13
  • 13
  • 12
  • 10
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA

Clone

608CT2-1-3
  • Binding Specificity

    • 15
    • 9
    • 8
    • 7
    • 6
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 287-314

    Purification

    Purified

    Immunogen

    A portion of amino acids 287-314 from the human protein was used as the immunogen for this ADA antibody.

    Isotype

    IgG1
  • Application Notes

    Titration of the ADA antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:100-1:250

    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 ADA antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    ADA (Adenosine Deaminase (ADA))

    Alternative Name

    ADA

    Background

    This gene encodes an enzyme that catalyzes the hydrolysis of adenosine to inosine. Various mutations have been described for this gene and have been linked to human diseases. Deficiency in this enzyme causes a form of severe combined immunodeficiency disease (SCID), in which there is dysfunction of both B and T lymphocytes with impaired cellular immunity and decreased production of immunoglobulins, whereas elevated levels of this enzyme have been associated with congenital hemolytic anemia.

    UniProt

    P00813

    Pathways

    Regulation of G-Protein Coupled Receptor Protein Signaling, Ribonucleoside Biosynthetic Process
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