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ADA antibody

This anti-ADA antibody is a Rabbit Polyclonal antibody detecting ADA in WB and IHC (p). Suitable for Human.
Catalog No. ABIN2854323

Quick Overview for ADA antibody (ABIN2854323)

Target

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

Reactivity

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

Host

  • 75
  • 20
  • 1
Rabbit

Clonality

  • 77
  • 19
Polyclonal

Conjugate

  • 52
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  • 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
  • 42
  • 15
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  • 9
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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Rabbit Polyclonal antibody to Adenosine Deaminase (adenosine deaminase)
    Adenosine Deaminase antibody

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

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

    Isotype

    IgG
  • Application Notes

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

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1XPBS ( pH 7), 20 % 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

    ADA (Adenosine Deaminase (ADA))

    Alternative Name

    adenosine deaminase

    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.

    Molecular Weight

    41 kDa

    Gene ID

    100

    UniProt

    P00813

    Pathways

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