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ASS1 antibody

ASS1 Reactivity: Human, Mouse, Rat WB, ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7245992
  • Target See all ASS1 Antibodies
    ASS1 (Argininosuccinate Synthase 1 (ASS1))
    Reactivity
    • 60
    • 16
    • 11
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 49
    • 8
    • 3
    Rabbit
    Clonality
    • 50
    • 10
    Polyclonal
    Conjugate
    • 39
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ASS1 antibody is un-conjugated
    Application
    • 47
    • 31
    • 27
    • 19
    • 12
    • 10
    • 6
    • 4
    • 3
    • 2
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Fusion protein of human ASS1
    Isotype
    IgG
    Top Product
    Discover our top product ASS1 Primary Antibody
  • Application Notes
    WB 1:500-1:2000, IHC 1:25-1:100, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    ASS1 (Argininosuccinate Synthase 1 (ASS1))
    Alternative Name
    ASS1 (ASS1 Products)
    Synonyms
    ASS antibody, CTLN1 antibody, AA408052 antibody, Ass-1 antibody, fold antibody, ASSA antibody, Ass antibody, ass antibody, zgc:92051 antibody, wu:fb95a04 antibody, wu:fc01e08 antibody, argininosuccinate synthase 1 antibody, argininosuccinate synthetase 1 antibody, argininosuccinate synthase 1 S homeolog antibody, ASS1 antibody, Ass1 antibody, ass1.S antibody, ass1 antibody
    Background
    ASS1 is a rate-limiting enzyme in the urea cycle. Citrullinemia type I is an autosomal recessive disorder that is caused by a deficiency of the urea cycle enzyme argininosuccinate synthetase (ASS1). Deficiency of ASS1 shows various clinical manifestations encompassing severely affected patients with fatal neonatal hyperammonemia as well as asymptomatic individuals with only a biochemical phenotype.
    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 47 kDa

    UniProt
    P00966
    Pathways
    Response to Growth Hormone Stimulus, Cellular Response to Molecule of Bacterial Origin
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