Adenylosuccinate Lyase/ADSL (clone AT16C10), anti-human

Adenylosuccinate Lyase/ADSL (clone AT16C10), anti-human

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In stock
SKU
ATGA0400
Catalog NumberATGA0400
Isotype
Mouse IgG1 kappa
Applications:
ELISA, WB, ICC/IF, FACS
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Description
Adenylosuccinate lyase, also known as ADSL, is an enzyme that converts adenylosuccinate to AMP and fumarate as part of the purine nucleotide cycle. Defects in ADSL are the cause of adenylosuccinase deficiency (ADSL deficiency). ADSL deficiency is an autosomal recessive disorder characterized by the accumulation in the body fluids of succinylaminoimidazole-carboxamide riboside (SAICA-riboside) and succinyladenosine (S-Ado).Alternative Names
Adenylosuccinate lyase, AMPS, ASASE, ASLConcentration
1mg/ml (determined by BCA assay)Concentration
Liquid in. Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% glycerolStorage: 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.
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