Descrizione Azione

A synthesized peptide derived from human ASK1, corresponding to a region within the internal amino acids.

Codice: DF6084 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human ASK1, corresponding to a region within the internal amino acids.

Codice: AF6477 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human ASK1, corresponding to a region within the internal amino acids.

Codice: BF8166 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human ASK1, corresponding to a region within N-terminal amino acids.

Codice: BF8930 Confezionamento: 100ul
Dettagli

A synthetic peptide from human ASK1

Codice: BF3379 Confezionamento: 100ul
Dettagli
Codice: A62114-100 Confezionamento: 100 µl
Dettagli
Codice: A62114-020 Confezionamento: 20 µl
Dettagli
Codice: A62114-050 Confezionamento: 50 µl
Dettagli

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.

Codice: E-AB-14601_120μL Confezionamento: 120μL
Dettagli

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.

Codice: E-AB-14601_200μL Confezionamento: 200μL
Dettagli

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.

Codice: E-AB-14601_20μL Confezionamento: 20μL
Dettagli

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.

Codice: E-AB-14601_60μL Confezionamento: 60μL
Dettagli