Phospho-PTS (S19) Recombinant Monoclonal Antibody

Code CSB-RA871518A0HU
Size US$210
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  • Overlay Peak curve showing HepG2 cells stained with CSB-RA871518A0HU (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100 for 10min. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*106cells) for 45min at 4℃. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 35min at 4℃.Control antibody (green line) was Rabbit IgG (1ug/1*106cells) used under the same conditions. Acquisition of >10, 000 events was performed.
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Product Details

Uniprot No.
Target Names
PTS
Alternative Names
6 pyruvoyl tetrahydrobiopterin synthase antibody; 6 pyruvoyl tetrahydropterin synthase antibody; 6 pyruvoyltetrahydropterin synthase antibody; 6-pyruvoyl tetrahydrobiopterin synthase antibody; EC 4.2.3.12 antibody; FLJ97081 antibody; OTTHUMP00000235385 antibody; PTP synthase antibody; PTPS antibody; PTPS_HUMAN antibody; PTS antibody
Species Reactivity
Human
Immunogen
A synthesized peptide from human PTS protein
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Monoclonal
Isotype
Rabbit IgG
Clone No.
18G10
Purification Method
Affinity-chromatography
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Rabbit IgG in 10mM phosphate buffered saline , pH 7.4, 150mM sodium chloride, 0.05% BSA, 0.02% sodium azide and 50% glycerol.
Form
Liquid
Tested Applications
ELISA, FC
Recommended Dilution
Application Recommended Dilution
FC 1:50-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Description

6-pyruvoyl tetrahydrobiopterin synthase, commonly known as PTS or PTPS, catalyzes the second step in the biosynthesis of tetrahydrobiopterin (BH4), an essential cofactor for aromatic amino acid hydroxylases and nitric oxide synthases. Phosphorylation at serine 19 represents a key regulatory modification that modulates enzyme activity and cellular BH4 levels, making this site particularly relevant for researchers investigating neurotransmitter biosynthesis, nitric oxide signaling, and metabolic disorders associated with BH4 deficiency.

This recombinant monoclonal antibody, clone 18G10, specifically recognizes the phosphorylated serine 19 residue of human PTS. Developed using recombinant technology and raised in rabbit, this antibody offers the consistency and reproducibility that phospho-specific detection demands. Each lot is derived from a defined sequence, eliminating the variability inherent in traditional hybridoma-based production and ensuring reliable performance across longitudinal studies where detecting subtle changes in phosphorylation status is critical.

Validation through flow cytometry demonstrates clear detection of phospho-PTS in HepG2 cells, with the overlay histogram showing distinct separation between the specific antibody signal and isotype control when used at 1:100 dilution. The protocol employed formaldehyde fixation with Triton X-100 permeabilization, providing researchers with an established workflow for intracellular phospho-protein detection in hepatocyte models.

For investigators exploring BH4-dependent pathways in neuroscience contexts, including studies of dopamine and serotonin synthesis regulation, this antibody provides a focused tool for monitoring PTS phosphorylation dynamics. The validated flow cytometry application enables quantitative, single-cell analysis of this post-translational modification in human cell populations.

Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Function
Involved in the biosynthesis of tetrahydrobiopterin, an essential cofactor of aromatic amino acid hydroxylases. Catalyzes the transformation of 7,8-dihydroneopterin triphosphate into 6-pyruvoyl tetrahydropterin.
Gene References into Functions
  1. Severe neurological impairment from BH4 deficiency could be prevented by newborn screening for hyperphenylalaninemia (HPA) and proper metabolic management. PMID: 19830588
  2. A total of 43 mutations were identified in the PTS gene in a screen of East Asian populations, comprising 22 previously reported mutations and 21 new discovered mutations. PMID: 22237589
  3. The mutant characterization of PTPS gene was coincident with other early studies in Chinese. The novel mutation L127F was considered as a pathogenetic mutation and associated with severe clinical phenotype. PMID: 18505119
  4. Our data show that PTPS induction is necessary for optimized BH4 synthesis in cytokine-stimulated human coronary artery endothelial cells and point to IL-1beta as a leading cytokine in this process. PMID: 14551150
  5. Hyperphenylalaninemia may be caused by deficiency of Phe hydroxylase or by deficiency of co-factor BH(4). PMID: 16086286
  6. Human PTS was efficiently expressed in noradrenergic regions but only in a small number of dopaminergic neurons. PMID: 16135092
  7. Expression of PTS was significantly decreased in PD cases. PMID: 17270157
  8. mutational analysis in Chinese hyperphenylalaninemia caused by tetrahydrobiopterin synthesis deficiency PMID: 11438997

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Involvement in disease
Hyperphenylalaninemia, BH4-deficient, A (HPABH4A)
Protein Families
PTPS family
Database Links

HGNC: 9689

OMIM: 261640

KEGG: hsa:5805

STRING: 9606.ENSP00000280362

UniGene: Hs.503860

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