Rat Carbamoyl Phosphate Synthetase 1 ELISA Kit | CPS1 elisa kit

Rat Carbamoyl Phosphate Synthetase 1 ELISA Kit

Cat. Num. AAA3809694

• Gene Names: CPS1; PHN; CPSASE1
• Reactivity: Rat
• Synonyms: Carbamoyl Phosphate Synthetase 1; Rat Carbamoyl Phosphate Synthetase 1 ELISA Kit; CPS1 elisa kit

• Reactivity: Rat
• Sequence Length: 1500

• Samples: Serum, plasma, cell culture supernate and other biological fluids
• Assay Type: Sandwich
• Detection Range: 62.5 ng/L-1000 ng/L
• Sensitivity: 1 ng/L

Typical Testing Data/Standard Curve (for reference only)

Related Product Information for CPS1 elisa kit

Intended Use: The Stop Solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. In order to measure the concentration ofCARBAMOYL PHOSPHATE SYNTHASE 1in the sample, This CARBAMOYL PHOSPHATE SYNTHASE 1ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a standard curve of Optical Density versusCARBAMOYL PHOSPHATE SYNTHASE 1concentration. The concentration ofCARBAMOYL PHOSPHATE SYNTHASE 1in the samples is then determined by comparing the O.D. of the samples to the standard curve.

NCBI and Uniprot Product Information

• NCBI GI #: 3228248
• NCBI GeneID: 1373
• NCBI Official Full Name: carbamoyl phosphate synthetase 1
• NCBI Official Synonym Full Names: carbamoyl-phosphate synthase 1
• NCBI Official Symbol: CPS1
• NCBI Official Synonym Symbols: PHN; CPSASE1
• NCBI Protein Information: carbamoyl-phosphate synthase [ammonia], mitochondrial
• Protein Family: Carboxypeptidase

NCBI Description

The mitochondrial enzyme encoded by this gene catalyzes synthesis of carbamoyl phosphate from ammonia and bicarbonate. This reaction is the first committed step of the urea cycle, which is important in the removal of excess urea from cells. The encoded protein may also represent a core mitochondrial nucleoid protein. Three transcript variants encoding different isoforms have been found for this gene. The shortest isoform may not be localized to the mitochondrion. Mutations in this gene have been associated with carbamoyl phosphate synthetase deficiency, susceptibility to persistent pulmonary hypertension, and susceptibility to venoocclusive disease after bone marrow transplantation.[provided by RefSeq, May 2010]