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ASL encodes a member of the lyase 1 family. Additionally we are shipping Argininosuccinate Lyase Proteins (13) and Argininosuccinate Lyase Kits (4) and many more products for this protein.
Showing 10 out of 50 products:
Human Monoclonal ASL Primary Antibody for IF, ELISA - ABIN559965
Syed, Langer, Janczar, Singh, Lo Nigro, Lattanzio, Coley, Hatzimichael, Bomalaski, Szlosarek, Awad, ONeil, Roncaroli, Crook: Epigenetic status of argininosuccinate synthetase and argininosuccinate lyase modulates autophagy and cell death in glioblastoma. in Cell death & disease 2013
Chicken Polyclonal ASL Primary Antibody for WB - ABIN2776928
Tanaka, Nagao, Mori, Tsutsumi: A novel stop codon mutation (X465Y) in the argininosuccinate lyase gene in a patient with argininosuccinic aciduria. in The Tohoku journal of experimental medicine 2003
Human Polyclonal ASL Primary Antibody for WB - ABIN2776927
Trevisson, Salviati, Baldoin, Toldo, Casarin, Sacconi, Cesaro, Basso, Burlina: Argininosuccinate lyase deficiency: mutational spectrum in Italian patients and identification of a novel ASL pseudogene. in Human mutation 2007
the mechanism induced by ASL (show ADSL Antibodies) shRNA which occurred in human breast cancer may be attributed to a decrease in cyclin A2 (show CCNA2 Antibodies) and NO.
The clinical and biochemical course in variant forms of ASL (show ADSL Antibodies) deficiency is associated with relevant residual levels of ASL (show ADSL Antibodies) activity as well as instability of mutant ASL (show ADSL Antibodies) proteins.
Point mutation of ASS1 (show ASS1 Antibodies), ASL (show ADSL Antibodies) and SLC25A13 (show slc25a13 Antibodies) is associated with citrullinemia (show ASS1 Antibodies).
Data show that in patients with Argininosuccinate lyase deficiency, the ASl (show ADSL Antibodies) gene is subject to several mutations, the majority are missense; some more frequent then others.
Our results suggest that ASL (show ADSL Antibodies) transcripts can contribute to the highly variable phenotype in ASA (show ARSA Antibodies) patients if expressed at high levels.
Cox (show COX8A Antibodies) regression analysis showed that ASL (show ADSL Antibodies) is an independent prognostic marker for HCC (show FAM126A Antibodies). Therefore, reduced ASL (show ADSL Antibodies) expression may be a novel maker for poor prognosis in HCC (show FAM126A Antibodies) patients
analysis of mutant argininosuccinate lyase in argininosuccinic aciduria
extent of protection of ASL (show ADSL Antibodies) and delta-crystallin at different ratios of alphaA-crystallin (show CRYAA Antibodies)
MDR analysis provided evidence of interaction between the genes for ASS1 (show ASS1 Antibodies) and SLC25A13 (show slc25a13 Antibodies) on the risk of CL/P.
Structural studies of the ASL (show ADSL Antibodies) frequently complementing allele Q286R suggest that the mutation may hinder a conformational change in the 280's loop (residues 270-290) and domain 3 that may be important for catalysis.
Enterocyte-derived ASL (show ADSL Antibodies) has a protective role in necrotizing enterocolitis.
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.
, delta crystallin II
, delta-2 crystallin