Anti-Mouse CD73 – Purified in vivo GOLD™ Functional Grade

Anti-Mouse CD73 – Purified in vivo GOLD™ Functional Grade

Product No.: C2413

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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

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Antibody Details

Product Details

Reactive 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.

Description

Description

Specificity
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 Advisor

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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 Studies

CD73 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 Controls

Comparative 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 Vivo

The 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 manufacturer’s specific instructions, which always take precedence. However, general best practices for sterile biological and microbiological cultures are as follows:

General Sterile Storage Guidelines

  • Room Temperatures: For many sterile reagents, especially those packaged for short-term use, the recommendation is to store between 18°C and 23°C (64–73°F), in a dry place with relative humidity between 30% and 60% to maintain integrity and prevent moisture damage.
  • Long-term Storage: If the clone is to be preserved for longer periods, typical laboratory practice is to store at refrigerated temperatures (2–8°C/36–46°F). However, some biological materials (especially heat-sensitive proteins or live cells) may require particular refrigeration regimes (e.g., 4°C) or even freezing.
  • Ultra-Low Freezing: For truly long-term storage, especially for viability-critical cultures, storage at ultra-low freezer temperatures (-70 to -80°C) or even in liquid nitrogen (-150°C and below) is standard for many microbial and eukaryotic cell lines.

Manufacturer’s Instructions Are Key

  • Always check the accompanying documentation or manufacturer’s label. The information above is a general guideline, but the clone TY/23 may have specific requirements or short shelf life outside certain temperatures.
  • If the material is supplied with a preservative or fixative, room temperature (15–27°C) may suffice, but this is rarely the case for live cultures or reagents for molecular work.
  • Sterile, lyophilized, or desiccated clones can often be stored refrigerated or even at room temperature, but again, only if explicitly stated by the manufacturer.

Summary Table

Storage TypeTemperature RangeSuitable For
Room Temperature (general)18–23°C (64–73°F)Short-term, sterile-packaged reagents
Refrigerated2–8°C (36–46°F)Biological cultures, short- to medium-term
Ultra-low Freezer-70 to -80°C (-94 to -112°F)Long-term, viability-critical samples
Cryogenic (LN2)-150°C and belowExtremely long-term storage

Always follow the manufacturer’s 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:

  • Anti-IL-17A antibodies: These are often used together with anti-IL-23 antibodies, particularly in studies of autoimmune and inflammatory diseases, because IL-17A and IL-23 function closely in the Th17 inflammatory pathway.

  • Anti-IL-12 antibodies: Since IL-12 and IL-23 both share the p40 subunit (IL-12 is p40/p35, IL-23 is p40/p19), antibodies against IL-12 (and specifically p40) are frequently used for specificity controls and to dissect individual cytokine roles in immune responses.

  • Bispecific antibodies targeting IL-17A and IL-23: These engineered proteins are designed to simultaneously block both cytokines, which can have additive or synergistic effects in neutralizing inflammatory pathways relevant to psoriasis and related disorders.

  • Protein scaffolds targeting IL-23: Recent publications highlight the use of engineered protein scaffolds such as Alphabodies, which specifically bind IL-23 with high affinity—distinguishing it from IL-12—and are studied as alternatives to traditional monoclonal antibodies.

In experimental setups with TY/23, typical combinations include:

  • Anti-IL-17A for pathway mapping in autoimmunity.
  • Anti-p40 (shared by IL-12 and IL-23) for specificity or blocking studies.
  • Other cytokine or cell marker antibodies (e.g., anti-IFN-?, anti-CD4, anti-CD3) for flow cytometry panels in immune cell phenotyping (not explicitly listed in the results, but commonly reported in immunological literature).
  • Engineered protein scaffolds for structure-function and inhibitor comparison studies.

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:

  1. Inhibition of Metastasis: TY/23 has been shown to inhibit metastasis significantly, demonstrating its potential as an anticancer agent. This suggests that targeting CD73 could be a valuable strategy in cancer treatment.

  2. Binding Affinity and Epitope Mapping: Studies have mapped the epitope of TY/23 and compared it with other anti-CD73 clones. It was found that TY/23 competes with other clones for binding to CD73, indicating a specific interaction with the CD73 protein.

  3. Enhanced Antitumor Activity: The blockade of CD73 by antibodies like TY/23 enhances the antitumor activity of other treatments, such as anti-PD-1 therapy. This suggests that combining CD73 blockade with existing immunotherapies could improve cancer treatment outcomes.

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 & Citations

1. 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.
FA
Flow Cytometry

Certificate of Analysis

Formats Available

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Disclaimer AlertProducts are for research use only. Not for use in diagnostic or therapeutic procedures.