PTS (Protein|Antibody|cDNA Clone|ELISA Kit)

All PTS reagents are produced in house and quality controlled, including 2 PTS Antibody, 28 PTS Gene, 1 PTS Protein, 1 PTS qPCR. All PTS reagents are ready to use.

Recombinant PTS proteins are expressed by E. coli with fusion tags as N-His.

PTSantibodies are validated with different applications, which are ELISA, IHC-P.

PTScDNA clones are full length sequence confirmed and expression validated. There are 13 kinds of tags for each PTS of different species, especially GFP tag, OFP tag, FLAG tag and so on. There are three kinds of vectors for choice, cloning vector, expression vector and lentivrial expression vector.

PTS Protein (1)


PTS Protein, Human, Recombinant (His Tag)


Expression host: E. coli

Human PTS Protein 10578

PTS Antibody (2)

Application Clonality

Anti-PTS Antibody


Application: ELISA,IHC-P

Clonality: PAb

Human PTS Immunohistochemistry(IHC) 7815

Anti-PTS Antibody


Application: ELISA

Clonality: MAb


PTS cDNA Clone (28)


PTS qPCR Primer (1)

PTS(6-pyruvoyltetrahydropterin synthase) belongs to the PTPS family. It catalyzes the elimination of inorganic triphosphate from dihydroneopterin triphosphate, which is the second and irreversible step in the biosynthesis of tetrahydrobiopterin from GTP. Tetrahydrobiopterin, also known as BH(4), is an essential cofactor and regulator of various enzyme activities, including enzymes involved in serotonin biosynthesis and NO synthase activity. Mutations in this gene result in hyperphenylalaninemia. PTS is involved in the biosynthesis of tetrahydrobiopterin, an essential cofactor of aromatic amino acid hydroxylases. PTS also catalyzes the transformation of 7,8-dihydroneopterin triphosphate into 6-pyruvoyl tetrahydropterin. Defects in PTS are the cause of BH4-deficient hyperphenylalaninemia type A (HPABH4A), also called 6-pyruvoyl-tetrahydropterin synthase deficiency (PTS deficiency) or hyperphenylalaninemia tetrahydrobiopterin-deficient due to PTS deficiency. HPABH4A is an autosomal recessive disorder characterized by depletion of the neurotransmitters dopamine and serotonin, and clinically by severe neurological symptoms unresponsive to the classic phenylalanine-low diet.