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ADSL Enzyme

Adenylosuccinate Lyase, ASL, Adenylosuccinase, ASase, AMPS

Catalog No. Product Name Size List Price (US$) Quantity
BP002560-ENZ-188 Recombinant Human Adenylosuccinate Lyase Enzyme 20 ug 160.00
BP002560-ENZ-188 Recombinant Human Adenylosuccinate Lyase Enzyme 1 mg 2700.00
Description

Introduction
Adenylosuccinate lyase (ADSL) is an enzyme which converts adenylosuccinate to AMP and fumarate as part of the purine nucleotide cycle. ADSL is involved in both de novo synthesis of purines and formation of adenosine monophosphate from inosine monophosphate. ADSL catalyzes 2 reactions in AMP biosynthesis: the removal of a fumarate from succinylaminoimidazole carboxamide (SAICA) ribotide to yield aminoimidazole carboxamide ribotide (AICA) and removal of fumarate from adenylosuccinate to yield AMP. Defects in the ADSL are the cause of adenylosuccinase deficiency (ADSL deficiency). ADSL deficiency is an autosomal recessive disorder distinguished by the accumulation in the body fluids of succinylaminoimidazole-carboxamide riboside (SAICA-riboside) and succinyladenosine (S-Ado). Adenylosuccinase deficiency results in succinylpurinemic autism, psychomotor retardation, and in some cases, growth retardation associated with muscle wasting and epilepsy.

BP002560-ENZ-188: Recombinant Human Adenylosuccinate Lyase (ADSL) Enzyme

Source: E. coli-derived.
A single, non-glycosylated polypeptide chain containing 520 amino acids (1-484) and having a molecular mass of 59 kDa. ADSL is fused to a 36 amino acid His-tag at N-terminus.
Purity: > 95.0% as determined by SDS-PAGE.
Formulation: The ADSL solution (1 mg/ml) contains 20 mM Tris-HCl buffer (pH 8.0), 1 mM DTT, 40% glycerol and 0.1 M NaCl.

Shipping: The product is shipped with ice pack. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70°C as supplied.

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