Anti-Thymidine Phosphorylase antibody [EPR25629-129] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal Thymidine Phosphorylase antibody. Carrier free. Suitable for ICC/IF, IP, WB, IHC-P, Flow Cyt (Intra) and reacts with Human samples.
View Alternative Names
ECGF1, TYMP, Thymidine phosphorylase, TP, Gliostatin, Platelet-derived endothelial cell growth factor, TdRPase, PD-ECGF
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-Thymidine Phosphorylase antibody [EPR25629-129] - BSA and Azide free (AB284863)
This data was developed using ab284861, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized A431 (Human epidermoid carcinoma epithelial cell) cells labelling Thymidine phosphorylase with ab284861 at 1/500 dilution (0.1ug)/(Red) compared with a Rabbit monoclonal IgG (ab172730)/(Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody)/(Blue). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Thymidine Phosphorylase antibody [EPR25629-129] - BSA and Azide free (AB284863)
This data was developed using ab284861, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human colon tissue labelling Thymidine phosphorylase with ab284861 at 1/5000 (0.103 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on the interstitial cells of human colon (PMID : 16361565). The section was incubated with ab284861 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Thymidine Phosphorylase antibody [EPR25629-129] - BSA and Azide free (AB284863)
This data was developed using ab284861, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized A431 cells labelling Thymidine phosphorylase with ab284861 at 1/50 (10.34 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/ml) dilution (Green). Confocal image showing cytoplasmic staining in A431 cells is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 (2.5 ug/ml) dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/ml) dilution.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Thymidine Phosphorylase antibody [EPR25629-129] - BSA and Azide free (AB284863)
This data was developed using ab284861, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized THP-1 cells labelling Thymidine phosphorylase with ab284861 at 1/50 (10.34 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/ml) dilution (Green). Confocal image showing cytoplasmic staining in THP-1 cells is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 (2.5 ug/ml) dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/ml) dilution.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Thymidine Phosphorylase antibody [EPR25629-129] - BSA and Azide free (AB284863)
This data was developed using ab284861, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human ovarian cancer tissue labelling Thymidine phosphorylase with ab284861 at 1/5000 (0.103 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on human ovarian cancer. The section was incubated with ab284861 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Thymidine Phosphorylase antibody [EPR25629-129] - BSA and Azide free (AB284863)
This data was developed using ab284861, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human tonsil tissue labelling Thymidine phosphorylase with ab284861 at 1/5000 (0.103 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on human tonsil. The section was incubated with ab284861 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins
- IP
Lab
Immunoprecipitation - Anti-Thymidine Phosphorylase antibody [EPR25629-129] - BSA and Azide free (AB284863)
This data was developed using ab284861, the same antibody clone in a different buffer formulation.
Thymidine phosphorylase was immunoprecipitated from 0.35 mg A431 (human epidermoid carcinoma epithelial cell) whole cell lysate 10 ug with ab284861 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab284861 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : A431 (human epidermoid carcinoma epithelial cell) whole cell lysate 10 ug
Lane 2 : ab284861 IP in A431 whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab284861 in A431 whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 10 seconds
All lanes:
Immunoprecipitation - Anti-Thymidine Phosphorylase antibody [EPR25629-129] (<a href='/en-us/products/primary-antibodies/thymidine-phosphorylase-antibody-epr25629-129-ab284861'>ab284861</a>)
Predicted band size: 50 kDa
Observed band size: 50 kDa
false
- WB
Lab
Western blot - Anti-Thymidine Phosphorylase antibody [EPR25629-129] - BSA and Azide free (AB284863)
This data was developed using ab284861, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Exposure time : 137 seconds
All lanes:
Western blot - Anti-Thymidine Phosphorylase antibody [EPR25629-129] (<a href='/en-us/products/primary-antibodies/thymidine-phosphorylase-antibody-epr25629-129-ab284861'>ab284861</a>) at 1/1000 dilution
All lanes:
A431 (human epidermoid carcinoma epithelial cell), whole cell lysate at 20 µg
Secondary
All lanes:
VeriBlot for IP secondary antibody(HRP)(<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Predicted band size: 50 kDa
Observed band size: 50 kDa
false
- WB
Lab
Western blot - Anti-Thymidine Phosphorylase antibody [EPR25629-129] - BSA and Azide free (AB284863)
This data was developed using ab284861, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Low expression : human ovary (PMID : 2328255).
The bands nearby 25 kDa could be non-specific bands.
Exposure time : Lane 1-3 : 3.25 seconds Lane 4-5 : 37 seconds
All lanes:
Western blot - Anti-Thymidine Phosphorylase antibody [EPR25629-129] (<a href='/en-us/products/primary-antibodies/thymidine-phosphorylase-antibody-epr25629-129-ab284861'>ab284861</a>) at 1/1000 dilution
Lane 1:
Human tonsil tissue lysate at 20 µg
Lane 2:
human ovary cancer tissue lysate at 20 µg
Lane 3:
human ovary tissue lysate at 20 µg
Lane 4:
human colon tissue lysate at 20 µg
Lane 5:
human liver tissue lysate at 20 µg
Secondary
All lanes:
Western blot - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/1000 dilution
Predicted band size: 50 kDa
Observed band size: 50 kDa
false
Related conjugates and formulations (1)
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Anti-Thymidine Phosphorylase antibody [EPR25629-129]
Reactivity data
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Why is this recommended?
We recommend this product because it’s often used in the same experiment or related research.
We advise that you always check the datasheet to ensure it fits your experiments, or contact ourtechnical teamfor help.
Product details
ab284863 is the carrier-free version of ab284861.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The enzyme participates in pyrimidine nucleoside metabolism providing an alternate route for thymidine catabolism. It is not part of a larger complex functioning independently to promote angiogenesis. Thymidine phosphorylase enhances the degradation of extracellular thymidine which can positively impact nucleotide balance within cells aiding DNA synthesis and repair.
Pathways
Thymidine phosphorylase operates significantly within the nucleotide salvage pathways. It is essential for clarifying thymidine availability for DNA synthesis. The enzyme links with enzymes like dihydropyrimidine dehydrogenase in pyrimidine degradation playing a critical role in maintaining cellular nucleotide homeostasis.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com