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ASS1 antibody (AA 1-412)

The Mouse Monoclonal anti-ASS1 antibody has been validated for WB, ELISA, IF and ICC. It is suitable to detect ASS1 in samples from Human.
Catalog No. ABIN5776060

Quick Overview for ASS1 antibody (AA 1-412) (ABIN5776060)

Target

See all ASS1 Antibodies
ASS1 (Argininosuccinate Synthase 1 (ASS1))

Reactivity

  • 80
  • 38
  • 34
  • 6
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 69
  • 9
  • 2
Mouse

Clonality

  • 48
  • 32
Monoclonal

Conjugate

  • 43
  • 6
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
This ASS1 antibody is un-conjugated

Application

  • 66
  • 53
  • 36
  • 31
  • 28
  • 17
  • 15
  • 9
  • 3
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)

Clone

AT1G11
  • Binding Specificity

    • 10
    • 8
    • 6
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-412

    Purpose

    Human ASS1 antibody

    Purification

    Purified

    Immunogen

    Recombinant human ASS1 (1-412aa) purified from E. coli

    Isotype

    IgG2a kappa
  • Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    Phosphate-Buffered Saline ( pH 7.4) with 0.02 % Sodium Azide, 10 % glycerol

    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,-80 °C

    Storage Comment

    Can be stored at +2C to +8C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
  • Target

    ASS1 (Argininosuccinate Synthase 1 (ASS1))

    Alternative Name

    ASS1

    Background

    ASS1 (argininosuccinate synthase or citrulline-aspartate ligase) belongs to the argininosuccinate synthase family. ASS1 is a urea cycle enzyme that is essential in the conversion of nitrogen from ammonia and aspartate to urea. A deficiency of ASS1 causes citrullinemia (CTLN1), an autosomal recessive disease which is characterized by severe vomiting spells and mental retardation. Cells deficient in ASS1 must absorb the arginine they need for growth from circulating blood.

    NCBI Accession

    NP_000041

    Pathways

    Response to Growth Hormone Stimulus, Cellular Response to Molecule of Bacterial Origin
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