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ASL antibody (AA 86-335)

The Rabbit Polyclonal anti-ASL antibody has been validated for WB and IHC. It is suitable to detect ASL in samples from Human.
Catalog No. ABIN1886687

Quick Overview for ASL antibody (AA 86-335) (ABIN1886687)

Target

See all ASL Antibodies
ASL (Argininosuccinate Lyase (ASL))

Reactivity

  • 60
  • 15
  • 11
  • 6
  • 6
  • 6
  • 6
  • 6
  • 5
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
Human

Host

  • 55
  • 5
Rabbit

Clonality

  • 57
  • 3
Polyclonal

Conjugate

  • 31
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ASL antibody is un-conjugated

Application

  • 40
  • 13
  • 13
  • 13
  • 12
  • 12
  • 7
  • 6
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 15
    • 12
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 86-335

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 86 and 335 of Human ASL
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.50-1.500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    ASL (Argininosuccinate Lyase (ASL))

    Alternative Name

    Argininosuccinate Lyase

    Background

    This gene encodes a member of the lyase 1 family.The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle.Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency.A nontranscribed pseudogene is also located on the long arm of chromosome 22.Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq]

    Molecular Weight

    49 kDa

    Gene ID

    435

    NCBI Accession

    NP_001020117, NM_001024946

    Pathways

    Response to Growth Hormone Stimulus
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