Immunohistochemistry (IHC) : Human colon carcinoma stained with anti-thymidylate synthase (TS) antibody using peroxidase-conjugate and DAB chromogen. Note the cytoplasmic staining of tumor cells.

mouse anti-Thymidylate Synthase (TS) monoclonal antibody (TS106) 6382

Price range: $160.00 through $528.00

Antibody summary

Mouse monoclonal to Thymidylate Synthase (TS)
Suitable for: Immunohistochemistry (formalin-fixed, paraffin-embedded tissues)
Reacts with: Human
Isotype:IgG1
Control: 5-FU resistant cancer
Visualization: Cytoplasmic
0.1, 0.5, 1.0 mL concentrated, 7 mL prediluted

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SKU: 6382parent Categories: antibody, Zeta IHC antibodies Tags: anatomy, General & Epithelial Markers, Thymidylate Synthase (TS)

Weight	1 lbs
Dimensions	9 × 5 × 2 in
host	mouse
isotype	IgG1
clonality	monoclonal
concentration	concentrate, predilute
applications	IHC
reactivity	human
available size	0.1 mL, 0.5 mL, 1 mL concentrated, 7 mL prediluted

mouse anti-Thymidylate Synthase (TS) monoclonal antibody TS106 6382

antibody
Database link: human P04818
Tested applications IHC
Recommended dilutions Concentrated 1:50
Application Notes Positive control: 5-FU resistant cancer
Immunogen Recombinant human thymidylate synthase
Size and concentration 7 mL prediluted or 0.1, 0.5, 1.0 mL and concentrated
Form liquid
Storage Instructions 2-8°C for short term, for longer term at -20°C. Avoid freeze / thaw cycles.
Purity affinity purified
Clonality monoclonal
Isotype IgG1
Compatible secondaries goat anti-mouse IgG, H&L chain specific, peroxidase conjugated polyclonal antibody 5486 goat anti-mouse IgG, H&L chain specific, biotin conjugated, Conjugate polyclonal antibody 2685 goat anti-mouse IgG, H&L chain specific, FITC conjugated polyclonal antibody 7854 goat anti-mouse IgG, H&L chain specific, peroxidase conjugated polyclonal antibody, crossabsorbed 1706 goat anti-mouse IgG, H&L chain specific, biotin conjugated polyclonal antibody, crossabsorbed 1716 goat anti-mouse IgG, H&L chain specific, FITC conjugated polyclonal antibody, crossabsorbed 1721
Isotype control Mouse monoclonal IgG1 - Isotype Control

target relevance
Protein names Thymidylate synthase (TS) (TSase) (EC 2.1.1.45)
Gene names TYMS,TYMS TS OK/SW-cl.29
Protein family Thymidylate synthase family
Mass 35716Da
Function FUNCTION: Catalyzes the reductive methylation of 2'-deoxyuridine 5'-monophosphate (dUMP) to thymidine 5'-monophosphate (dTMP), using the cosubstrate, 5,10- methylenetetrahydrofolate (CH2H4folate) as a 1-carbon donor and reductant and contributes to the de novo mitochondrial thymidylate biosynthesis pathway. {ECO:0000269\|PubMed:11278511, ECO:0000269\|PubMed:21876188}.
Catalytic activity CATALYTIC ACTIVITY: Reaction=dUMP + (6R)-5,10-methylene-5,6,7,8-tetrahydrofolate = 7,8-dihydrofolate + dTMP; Xref=Rhea:RHEA:12104, ChEBI:CHEBI:15636, ChEBI:CHEBI:57451, ChEBI:CHEBI:63528, ChEBI:CHEBI:246422; EC=2.1.1.45; Evidence={ECO:0000269\|PubMed:11278511}; PhysiologicalDirection=left-to-right; Xref=Rhea:RHEA:12105; Evidence={ECO:0000305\|PubMed:11278511};
Pathway PATHWAY: Pyrimidine metabolism; dTTP biosynthesis. {ECO:0000305\|PubMed:11278511}.
Subellular location SUBCELLULAR LOCATION: Nucleus {ECO:0000269\|PubMed:21876188}. Cytoplasm {ECO:0000269\|PubMed:21876188}. Mitochondrion {ECO:0000269\|PubMed:21876188}. Mitochondrion matrix {ECO:0000269\|PubMed:21876188}. Mitochondrion inner membrane {ECO:0000269\|PubMed:21876188}.
Structure SUBUNIT: Homodimer. {ECO:0000250\|UniProtKB:P45352}.
Involvement in disease DISEASE: Dyskeratosis congenita, digenic (DKCD) [MIM:620040]: A form of dyskeratosis congenita, a rare multisystem disorder caused by defective telomere maintenance. It is characterized by progressive bone marrow failure, and the clinical triad of reticulated skin hyperpigmentation, nail dystrophy, and mucosal leukoplakia. Common but variable features include premature graying, aplastic anemia, low platelets, osteoporosis, pulmonary fibrosis, and liver fibrosis among others. Early mortality is often associated with bone marrow failure, infections, fatal pulmonary complications, or malignancy. DKCD transmission pattern is consistent with digenic inheritance. {ECO:0000269\|PubMed:35931051}. Note=The disease is caused by variants affecting distinct genetic loci, including the gene represented in this entry. TYMS germline variants in the presence of a common ENOSF1 haplotype (defined by rs699517, rs2790 and rs1512643) result in severe thymidylate synthase deficiency and disease. The pathogenic mechanism involves increased expression of ENOSF1 relative to TYMS, and post-transcriptional inhibition of TYMS translation through ENOSF1-TYMS RNA-RNA interactions. {ECO:0000269\|PubMed:35931051}.
Target Relevance information above includes information from UniProt accession: P04818
The UniProt Consortium

Data

Human colon carcinoma stained with anti-thymidylate synthase (TS) antibody using peroxidase-conjugate and DAB chromogen. Note the cytoplasmic staining of tumor cells.

FAQ & Publications

Frequently Asked Questions

What applications is the mouse anti-Thymidylate Synthase (TS) monoclonal antibody (TS106) validated for?

This antibody is validated for use in immunohistochemistry (IHC) on formalin-fixed, paraffin-embedded human tissue samples.

How should the mouse anti-Thymidylate Synthase (TS) antibody be stored to maintain stability?

For short-term storage, keep the antibody at 2-8°C. For longer-term preservation, store it at -20°C and avoid repeated freeze/thaw cycles to maintain antibody integrity.

What species does the anti-Thymidylate Synthase (TS) monoclonal antibody (TS106) react with?

The antibody is reactive with human Thymidylate Synthase and is suitable for detecting human tissue samples.

What is the recommended dilution for using the concentrated form of the TS106 antibody in IHC?

The concentrated antibody should be diluted at a ratio of 1:50 for optimal immunohistochemical staining results.

Publications

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We haven't added any publications to our database yet.

Published literature highly relevant to the biological target of this product and referencing this antibody or clone are retrieved from the PubMed database provided by the United States National Library of Medicine at the National Institutes of Health.