Anti-Mouse CD73 – Purified in vivo GOLD™ Functional Grade
Anti-Mouse CD73 – Purified in vivo GOLD™ Functional Grade
Product No.: C2413
Clone TY/23 Target CD73 Formats AvailableView All Product Type Hybridoma Monoclonal Antibody Alternate Names Ecto-5'-nucleotidase Isotype Rat IgG2a κ Applications FA , FC |
Antibody DetailsProduct DetailsReactive Species Mouse Host Species Rat Recommended Isotype Controls Recommended Dilution Buffer Immunogen BALB/c mouse splenocytes and CHO cells transfected with the mouse CD73 gene Product Concentration ≥ 5.0 mg/ml Endotoxin Level < 1.0 EU/mg as determined by the LAL method Purity ≥95% monomer by analytical SEC ⋅ >95% by SDS Page Formulation This monoclonal antibody is aseptically packaged and formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 - 7.4 with no carrier protein, potassium, calcium or preservatives added. Due to inherent biochemical properties of antibodies, certain products may be prone to precipitation over time. Precipitation may be removed by aseptic centrifugation and/or filtration. State of Matter Liquid Product Preparation Functional grade preclinical antibodies are manufactured in an animal free facility using only in vitro protein free cell culture techniques and are purified by a multi-step process including the use of protein A or G to assure extremely low levels of endotoxins, leachable protein A or aggregates. Storage and Handling Functional grade preclinical antibodies may be stored sterile as received at 2-8°C for up to one month. For longer term storage, aseptically aliquot in working volumes without diluting and store at ≤ -70°C. Avoid Repeated Freeze Thaw Cycles. Regulatory Status Research Use Only Country of Origin USA Shipping 2 – 8° C Wet Ice Additional Applications Reported In Literature ? FA, FC Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change. DescriptionDescriptionSpecificity Ty/23 activity is directed against mouse CD73, also known as ecto-5′-nucleotidase (5′-NT). Background CD73 is a 69 kDa cell-surface protein anchored to the membrane by a GPI (glycosylphosphatidylinositol) anchor. CD73 plays a vital role in modulating the immune response by converting AMP (adenosine monophosphate) to adenosine. This conversion shifts the environment from being pro-inflammatory to anti-inflammatory. CD73 is particularly involved in the immunosuppressive activity of regulatory T cells. It catalyzes the dephosphorylation of extracellular nucleoside 5' monophosphates to nucleosides1,2. CD73 is expressed on specific subsets of T and B lymphocytes, with the highest expression found on B cells and CD8+ T cells. It is also implicated in cell activation, lymphocyte homing, and cell adhesion3. Moreover, CD73 has protective functions in various organ systems and cell types. For instance, it plays anti-nociceptive roles in the central nervous system and barrier-preserving roles in the respiratory system4. The TY/23 clone has been demonstrated to inhibit the enzymatic activity of CD73. Therefore, it is a valuable tool for studying the role of CD73 in immune regulation and its potential as a therapeutic target5. This clone has been utilized for both in vivo and in vitro CD73 blockade, contributing significantly to our understanding of how CD73 impacts immune responses and tumor microenvironments6. CD73 is a key player in the tumor microenvironment, and inhibiting its activity has been suggested as a potential strategy for cancer immunotherapy7. Tumors exploit CD73 to generate adenosine, which then suppresses T-cell responses against the tumor. By targeting CD73 and inhibiting its function, it is believed that tumorigenesis can be reduced, and T-cell-directed therapies can be enhanced8. Antigen Distribution CD73 is expressed on subsets of T and B lymphocytes, with the highest expression
on B cells and CD8+ T cells. Ligand/Receptor Nucleoside 5' monophosphate NCBI Gene Bank ID UniProt.org Research Area Costimulatory Molecules . Immunology Leinco Antibody AdvisorPowered by AI: AI is experimental and still learning how to provide the best assistance. It may occasionally generate incorrect or incomplete responses. Please do not rely solely on its recommendations when making purchasing decisions or designing experiments. The TY/23 clone is used in multiple ways in in vivo mouse studies, primarily as a tool for CD73 blockade and functional inhibition in cancer immunotherapy research. Primary Applications in Mouse StudiesCD73 Enzymatic Blockade: The TY/23 antibody serves as a blocking agent to inhibit CD73's enzymatic activity in vivo. CD73 converts AMP to adenosine, creating an immunosuppressive environment that shifts from ATP-driven pro-inflammatory conditions to anti-inflammatory states induced by adenosine. By blocking this conversion, TY/23 helps maintain a more pro-inflammatory, anti-tumor immune environment. Cancer Immunotherapy Enhancement: TY/23 is frequently used in combination with other immunotherapies, particularly anti-PD-1 treatments, to enhance antitumor activity. The antibody targets the immunosuppressive mechanisms that tumors use to evade immune responses, making it a valuable tool for studying combination immunotherapy approaches. Experimental Design and ControlsComparative Studies: Researchers use TY/23 alongside other anti-CD73 clones to compare different approaches to CD73 targeting. In epitope mapping studies, TY/23 serves as a reference standard against which newly developed anti-CD73 antibodies are compared for binding specificity and functional overlap. Flow Cytometry Applications: While TY/23 is used for functional blockade in vivo, different clones like TY/11.8 are often employed for flow cytometry analysis in the same studies, allowing researchers to monitor CD73 expression while simultaneously blocking its function. Mechanism of Action in VivoThe TY/23 clone specifically targets mouse CD73, a 69 kDa GPI-anchored cell-surface protein expressed on CD11b+ myeloid cells in bone marrow and T cells in the spleen. By binding to CD73 and inhibiting its enzymatic activity, TY/23 prevents the production of immunosuppressive adenosine, thereby maintaining immune cell activation and enhancing antitumor responses. This mechanism is particularly important for counteracting the immunosuppressive activity of regulatory T cells, where CD73 plays a strategic role in immune regulation. The correct storage temperature for sterile packaged items like a clone TY/23 (assuming it is a microbiologically certified culture or similar biological reagent maintained sterile for laboratory use) depends on the manufacturers specific instructions, which always take precedence. However, general best practices for sterile biological and microbiological cultures are as follows: General Sterile Storage Guidelines
Manufacturers Instructions Are Key
Summary Table
Always follow the manufacturers storage instructions for clone TY/23. If no specific guidance is available, refrigeration at 4°C is generally safe for sterile, packaged biological cultures, but confirm with the supplier for optimal results. Improper storage can lead to loss of viability or contamination, even if the package remains unopened. Alongside TY/23 (an antibody targeting IL-23, specifically its p19 subunit), researchers frequently use other antibodies and proteins that target related cytokines, subunits, or immunological markers in the literature. The most commonly used reagents include:
In experimental setups with TY/23, typical combinations include:
These combinations are used to delineate the roles of IL-23 in disease, compare the effects of blocking different cytokines, and to develop more effective therapies for autoimmune conditions. Clone TY/23 is a monoclonal antibody (mAb) that targets CD73, a protein involved in cancer and immune responses. Key findings from its citations in scientific literature include:
Overall, TY/23 is highlighted for its role in inhibiting cancer progression and potentially enhancing the effectiveness of other cancer treatments when used in combination. References & Citations1. Resta R, Thompson LF. Cell Signal. 1997;9(2):131-139. 2. Resta R, Yamashita Y, Thompson LF. Immunol Rev. 1998;161:95-109. 3. Thomson LF, Ruedi JM, Glass A, et al. Tissue Antigens. 1990;35(1):9-19. 4. Minor M, Alcedo KP, Battaglia RA, Snider NT. Am J Physiol Cell Physiol. 2019;317(6):C1079-C1092. 5. Roh M, Wainwright DA, Wu JD, Wan Y, Zhang B. Curr Opin Pharmacol. 2020;53:66-76. 6. Piccione EC, Mikesell G, Daine-Matsuoka B, Walter K, Miller R, McCaffery I. Cancer Research.2017;77(13_Supplement):5577. 7. Ghalamfarsa G, Kazemi MH, Raoofi Mohseni S, et al. Expert Opin Ther Targets. 2019;23(2):127-142. 8. Beavis PA, Stagg J, Darcy PK, Smyth MJ. Trends Immunol. 2012;33(5):231-237. 9. Zhang F, Li R, Yang Y, et al. Immunity. 2019;50(3):738-750.e7. 10. Allard B, Turcotte M, Spring K, Pommey S, Royal I, Stagg J. Int J Cancer. 2014;134(6):1466-1473. 11. Allard B, Pommey S, Smyth MJ, Stagg J. Clin Cancer Res. 2013;19(20):5626-5635. 12. Yamashita Y, Hooker SW, Jiang H, et al. Eur J Immunol. 1998;28(10):2981-2990. Technical ProtocolsCertificate of Analysis |
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