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

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

Product No.: C2413

[product_table name="All Top" skus="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

- -
- -
Select Product Size
- -
- -

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

Powered 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.

Clone TY/23 is a rat IgG2a monoclonal antibody that specifically targets mouse CD73 (ecto-5'-nucleotidase), and it has several important in vivo applications in murine research models.

Primary In Vivo Application

The most common in vivo application of clone TY/23 is CD73 blockade in mouse models. CD73 plays a critical role in converting extracellular AMP to adenosine, which shifts the immune environment from an ATP-driven proinflammatory state to an anti-inflammatory milieu induced by adenosine. By blocking CD73 enzymatic activity, the TY/23 antibody can modulate this immunosuppressive pathway.

Cancer and Immunotherapy Research

Clone TY/23 is particularly valuable in cancer immunology studies where CD73-mediated immunosuppression is a therapeutic target. Since CD73 is important for the immunosuppressive activity of regulatory T cells, blocking this pathway with TY/23 can potentially enhance anti-tumor immune responses. The antibody enables researchers to investigate how inhibiting adenosine production affects tumor growth, immune cell infiltration, and the efficacy of other immunotherapies in mouse models.

Immune Regulation Studies

The TY/23 antibody is used to study purinergic signaling and immune regulation in various disease contexts. In mice, CD73 expression is restricted to CD11b+ myeloid cells in the bone marrow and T cells in the spleen, making TY/23 useful for investigating how CD73 modulates immune responses, inflammation, and tissue repair processes in these cellular compartments.

The antibody has been validated for in vivo use with proper formulation (low endotoxin preparations available), ensuring it can be safely administered to mice for functional blockade experiments without confounding inflammatory effects from endotoxin contamination.

When discussing antibodies or proteins used in conjunction with or related to IL-23 (referred to as "TY/23" in the query, potentially a typographical error), several proteins and antibodies are commonly mentioned in the literature. Here are a few examples:

Antibodies and Proteins Related to IL-23

  1. Alphabodies: These are protein scaffolds designed to target IL-23, a cytokine involved in autoimmune diseases like psoriasis and multiple sclerosis. Alphabodies specifically bind to the p19 subunit of IL-23, neutralizing its activity.

  2. Bispecific Antibodies Targeting IL-17A and IL-23: These are engineered antibodies that simultaneously target IL-17A and IL-23, both of which are cytokines involved in inflammatory pathways. Phage display is a common method for engineering such antibodies.

  3. Single-Domain Antibodies (VHHs): While not specifically targeting IL-23, VHHs are being explored for their stability and potential in oral delivery, including targeting related pathways like IL-23R.

  4. Tandem Single-Chain Variable Fragments (scFv2): These are components of bispecific antibodies and can be engineered to target multiple antigens, potentially including cytokines in the IL-23 pathway.

Other Relevant Proteins

  1. IL-12: This cytokine is closely related to IL-23 and is sometimes targeted alongside IL-23 in therapeutic strategies. However, Alphabodies are designed to distinguish between IL-23 and IL-12, ensuring specificity for IL-23.

  2. IL-17A: Often targeted alongside IL-23 due to its role in inflammatory diseases, IL-17A is a key cytokine involved in the pathogenesis of conditions like psoriasis.

These proteins and antibodies are used in various therapeutic and diagnostic applications, often focusing on modulating immune responses in autoimmune diseases.

Clone TY/23 is a rat IgG2a monoclonal antibody used extensively in scientific literature for its ability to target CD73, a surface protein involved in various biological processes. The key findings from citations involving clone TY/23 include:

  1. CD73 Targeting: TY/23 is known for binding to CD73, which is a 69 kDa GPI-anchored surface protein involved in the breakdown of AMP to adenosine, playing a role in immune regulation and tumor microenvironments.

  2. Tumor Metastasis Inhibition: Studies have shown that TY/23 can significantly inhibit metastasis in cancer models, highlighting its potential in cancer therapy by targeting CD73-expressing cells.

  3. Epitope Mapping: TY/23 has been used as a reference for epitope mapping of other anti-CD73 clones. It is part of an epitope bin that overlaps with clones CD73–04 and 2C5, suggesting functional similarities.

  4. Flow Cytometry Applications: TY/23 is also used in flow cytometry for detecting CD73 expression on cells, providing a tool for studying CD73's role in different cell types.

Overall, TY/23 is a valuable tool in cancer research and immunological studies, particularly for its ability to target CD73 and contribute to understanding its role in various biological processes.

Unfortunately, the search results do not provide specific information on the dosing regimens of clone TY/23 across different mouse models. Clone TY/23 is not mentioned in the provided search results, and there is no detailed information available on its dosing in mouse models. For accurate dosing information, consulting specific scientific literature or contacting researchers who have worked with clone TY/23 would be advisable.

However, general guidelines for dosing antibodies in mouse models, such as those for PD-1, PD-L1, and CTLA-4 checkpoint blockade antibodies, are available:

  • PD-1 (e.g., RMP1-14 or 29F.1A12): Typically dosed at 100-500 μg per mouse, with an intraperitoneal injection schedule of every 3-4 days.
  • PD-L1 (e.g., 10F.9G2): Dosed at 100-250 μg per mouse, with a schedule of 2-3 times per week.
  • CTLA-4 (e.g., 9H10 or 9D9): Doses range from 100-250 μg per mouse, injected every 3 days.

These examples illustrate how dosing regimens can vary based on the target and application in mouse models.

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

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