
Description of target: 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.;Species reactivity: Human;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 39pg/mL
Vyberte, čo potrebujete, a my sa vám ozveme

S pribudajucim vekom sa zvysuje riziko vzniku mnohych ochoreni. Okrem zmien sposobenych prirodzenym ...
Čítať viac
V mnohých médiách čoraz častejšie počujeme o autoimunitných ochoreniach alebo o samotnej autoimunite...
Čítať viac
S prichodom leta zacina kvitnut mnozstvo rastlin. Pocet pelovych zrn vo vzduchu sa zvysuje a vcely i...
Čítať viac