Home Antibody All anti-ASL antibodies
|Recombinant protein fragment contain a sequence corresponding to a region within amino acids 13 and 231 of Argininosuccinate Lyase|
|0.1M Tris, 0.1M Glycine, 10% Glycerol (pH7). 0.01% Thimerosal was added as a preservative.|
|Purified by antigen-affinity chromatography.
|Homo sapiens argininosuccinate lyase (ASL), transcript variant 2|
|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. [provided by RefSeq]|
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A: Hela B: HepG2 (anti-ASL antibody diluted at 1:1000)
Immunofluorescence analysis of paraformaldehyde-fixed HeLa, using Argininosuccinate Lyase(anti-ASL antibody) antibody at 1:200 dilution.