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ADA antibody (C-Term)

This anti-ADA antibody is a Mouse Monoclonal antibody detecting ADA in WB. Suitable for Human.
Catalog No. ABIN1536621

Quick Overview for ADA antibody (C-Term) (ABIN1536621)

Target

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

Reactivity

  • 62
  • 33
  • 17
  • 14
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 72
  • 18
  • 1
Mouse

Clonality

  • 74
  • 17
Monoclonal

Conjugate

  • 47
  • 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

  • 80
  • 39
  • 14
  • 13
  • 13
  • 13
  • 12
  • 11
  • 7
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

608CT2-1-3
  • Binding Specificity

    • 15
    • 8
    • 8
    • 7
    • 5
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 287-314, C-Term

    Purification

    This antibody is purified through a protein G column, followed by dialysis against PBS.

    Immunogen

    This ADA antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 287-314 amino acids from the C-terminal region of human ADA.

    Isotype

    IgG1
  • Application Notes

    WB: 1:100~250

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified monoclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Storage Comment

    ADA Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Expiry Date

    6 months
  • 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.

    Molecular Weight

    40764

    Gene ID

    100

    NCBI Accession

    NP_000013

    UniProt

    P00813

    Pathways

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