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ASL antibody

The Rabbit Polyclonal anti-ASL antibody is suitable to detect ASL in samples from Human, Mouse and Rat. It has been validated for ELISA and IHC.
Catalog No. ABIN7240532
$538.80
Plus shipping costs $50.00
Shipping to: United States
Delivery in 11 to 14 Business Days

Quick Overview for ASL antibody (ABIN7240532)

Target

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

Reactivity

  • 60
  • 14
  • 10
  • 6
  • 6
  • 6
  • 6
  • 6
  • 5
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
Human, Mouse, Rat

Host

  • 54
  • 6
Rabbit

Clonality

  • 56
  • 4
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

  • 41
  • 13
  • 13
  • 11
  • 11
  • 11
  • 7
  • 6
  • 5
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant protein of human ASL

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.2 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    ASL (Argininosuccinate Lyase (ASL))

    Alternative Name

    ASL

    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.

    UniProt

    P04424

    Pathways

    Response to Growth Hormone Stimulus
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