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ASL encodes a member of the lyase 1 family. Additionally we are shipping Argininosuccinate Lyase Antibodies (54) and Argininosuccinate Lyase Kits (4) and many more products for this protein.
Showing 10 out of 13 products:
Human ASL Protein expressed in Escherichia coli (E. coli) - ABIN667597
Zhao, Xu, Jiang, Yu, Lin, Zhang, Yao, Zhou, Zeng, Li, Li, Shi, An, Hancock, He, Qin, Chin, Yang, Chen, Lei, Xiong, Guan: Regulation of cellular metabolism by protein lysine acetylation. in Science (New York, N.Y.) 2010
Show all 2 references for ABIN667597
the mechanism induced by ASL (show ADSL Proteins) shRNA which occurred in human breast cancer may be attributed to a decrease in cyclin A2 (show CCNA2 Proteins) and NO.
The clinical and biochemical course in variant forms of ASL (show ADSL Proteins) deficiency is associated with relevant residual levels of ASL (show ADSL Proteins) activity as well as instability of mutant ASL (show ADSL Proteins) proteins.
Point mutation of ASS1 (show ASS1 Proteins), ASL (show ADSL Proteins) and SLC25A13 (show slc25a13 Proteins) is associated with citrullinemia (show ASS1 Proteins).
Data show that in patients with Argininosuccinate lyase deficiency, the ASl (show ADSL Proteins) gene is subject to several mutations, the majority are missense; some more frequent then others.
Our results suggest that ASL (show ADSL Proteins) transcripts can contribute to the highly variable phenotype in ASA (show ARSA Proteins) patients if expressed at high levels.
Cox (show COX8A Proteins) regression analysis showed that ASL (show ADSL Proteins) is an independent prognostic marker for HCC (show FAM126A Proteins). Therefore, reduced ASL (show ADSL Proteins) expression may be a novel maker for poor prognosis in HCC (show FAM126A Proteins) patients
analysis of mutant argininosuccinate lyase in argininosuccinic aciduria
extent of protection of ASL (show ADSL Proteins) and delta-crystallin at different ratios of alphaA-crystallin (show CRYAA Proteins)
MDR analysis provided evidence of interaction between the genes for ASS1 (show ASS1 Proteins) and SLC25A13 (show slc25a13 Proteins) on the risk of CL/P.
Structural studies of the ASL (show ADSL Proteins) 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 Proteins) 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