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P5CS antibody (N-Term)

This anti-P5CS antibody is a Rabbit Polyclonal antibody detecting P5CS in WB. Suitable for Human.
Catalog No. ABIN631032

Quick Overview for P5CS antibody (N-Term) (ABIN631032)

Target

See all P5CS (ALDH18A1) Antibodies
P5CS (ALDH18A1) (Aldehyde Dehydrogenase 18 Family, Member A1 (ALDH18A1))

Reactivity

  • 21
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 16
  • 4
  • 1
Rabbit

Clonality

  • 19
  • 2
Polyclonal

Conjugate

  • 16
  • 1
  • 1
  • 1
  • 1
  • 1
This P5CS antibody is un-conjugated

Application

  • 21
  • 14
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 7
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    Specificity

    ALDH18 A1 antibody was raised against the N terminal of ALDH18 1

    Purification

    Affinity purified

    Immunogen

    ALDH18 A1 antibody was raised using the N terminal of ALDH18 1 corresponding to a region with amino acids SVIRHVRSWSNIPFITVPLSRTHGKSFAHRSELKHAKRIVVKLGSAVVTR
  • Application Notes

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    ALDH18A1 Blocking Peptide, (ABIN5612007), is also available for use as a blocking control in assays to test for specificity of this ALDH18A1 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of ALDH10 1 antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Handling Advice

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target

    P5CS (ALDH18A1) (Aldehyde Dehydrogenase 18 Family, Member A1 (ALDH18A1))

    Alternative Name

    ALDH18A1

    Background

    This gene is a member of the aldehyde dehydrogenase family and encodes a bifunctional ATP- and NADPH-dependent mitochondrial enzyme with both gamma-glutamyl kinase and gamma-glutamyl phosphate reductase activities. The encoded protein catalyzes the reduction of glutamate to delta1-pyrroline-5-carboxylate, a critical step in the de novo biosynthesis of proline, ornithine and arginine. Mutations in this gene lead to hyperammonemia, hypoornithinemia, hypocitrullinemia, hypoargininemia and hypoprolinemia and may be associated with neurodegeneration, cataracts and connective tissue diseases.

    Molecular Weight

    87 kDa (MW of target protein)
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