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ASL antibody (AA 13-231)

This Rabbit Polyclonal antibody specifically detects ASL in WB, IHC and IF. It exhibits reactivity toward Human.
Catalog No. ABIN1886011

Quick Overview for ASL antibody (AA 13-231) (ABIN1886011)

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
  • 11
  • 7
  • 6
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

    • 15
    • 12
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 13-231

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 13 and 231 of Argininosuccinate Lyase
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.100-1.500
    Immunofluorescence: 1.100-1.200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 20 % 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

    52 kDa

    Gene ID

    435

    Pathways

    Response to Growth Hormone Stimulus
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