Anti-Mouse/Human CD273 (PD-L2) [Clone 3.2.B8] — Purified in vivo PLATINUM™ Functional Grade

Anti-Mouse/Human CD273 (PD-L2) [Clone 3.2.B8] — Purified in vivo PLATINUM™ Functional Grade

Product No.: P679

[product_table name="All Top" skus="P379"]

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Clone
3.2.B8
Target
PD-L2
Formats AvailableView All
Product Type
Monoclonal Antibody
Alternate Names
B7-DC, CD273, PDL2, B7DC, Clone 3.2
Isotype
Mouse IgG1
Applications
B
,
FC
,
in vivo
,
WB

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Select Product Size

Data

Recombinant Human PD-L2 (CD273) SDS PAGE data
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Antibody Details

Product Details

Reactive Species
Human
Mouse
Host Species
Mouse
Recommended Dilution Buffer
Immunogen
Made in PD-L2 knockout mouse fusion partner X63-Ag8.653 myeloma cells
Product Concentration
≥ 5.0 mg/ml
Endotoxin Level
<0.5 EU/mg as determined by the LAL method
Purity
≥98% 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.
Product Preparation
Functional grade preclinical antibodies are manufactured in an animal free facility using in vitro 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.
Pathogen Testing
To protect mouse colonies from infection by pathogens and to assure that experimental preclinical data is not affected by such pathogens, all of Leinco’s Purified Functional PLATINUM™ antibodies are tested and guaranteed to be negative for all pathogens in the IDEXX IMPACT I Mouse Profile.
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.
Country of Origin
USA
Shipping
Next Day 2-8°C
Applications and Recommended Usage?
Quality Tested by Leinco
Western Blot: For Western blot analysis at a concentration of 1.0-2.0 µg/ml when used in conjunction with compatible secondary reagents
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
Clone 3.2.B8 recognizes an epitope on mouse/human PD-L2 and has been shown to bind to both mouse and human PD-L2 equally well
Background
PD-1 is a 50-55 kD member of the B7 Ig superfamily. PD-1 is also a member of the extended CD28/CTLA-4 family of T cell regulators and is suspected to play a role in lymphocyte clonal selection and peripheral tolerance. The ligands of PD-1 are PD-L1 and PD-L2, and are also members of the B7 Ig superfamily. PD-1 and its ligands negatively regulate immune responses. PD-L1, or B7-Homolog 1, is a 40 kD type I transmembrane protein that has been reported to costimulate T cell growth and cytokine production. The interaction of PD-1 with its ligand PD-L1 is critical in the inhibition of T cell responses that include T cell proliferation and cytokine production. PD-L1 has increased expression in several cancers. Inhibition of the interaction between PD-1 and PD-L1 can serve as an immune checkpoint blockade by improving T-cell responses In vitro and mediating preclinical antitumor activity. Within the field of checkpoint inhibition, combination therapy using anti-PD1 in conjunction with anti-CTLA4 has significant therapeutic potential for tumor treatments. PD-L2 is a 25 kD type I transmembrane ligand of PD-1. Via PD-1, PD-L2 can serve as a co-inhibitor of T cell functions. Regulation of T cell responses, including enhanced T cell proliferation and cytokine production, can result from mAbs that block the PD-L2 and PD-1 interaction.
Antigen Distribution
PD-L2 is expressed on dendritic cells, liver, few transformed cell lines, and a subset of macrophages.
Ligand/Receptor
PD-1
Function
Binds to PD-1 and alternative receptor
NCBI Gene Bank ID
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.

Use of Clone 3.2.B8 (Anti-CD273/PD-L2) in In Vivo Mouse Studies

Clone 3.2.B8 is a monoclonal antibody that binds to both mouse and human PD-L2 (also known as CD273), recognizing the same epitope on both species with equal affinity. It is supplied as Purified in vivo GOLD™ or PLATINUM™ Functional Grade, indicating it is specifically processed for in vivo use—ensuring low endotoxin levels and high purity for animal studies.

Applications and Purpose

  • Immune Checkpoint Studies: PD-L2, like PD-L1, is a ligand for the immune checkpoint receptor PD-1. The PD-1/PD-L2 interaction plays a role in immune suppression, particularly in the context of T cell regulation and tumor immune evasion. By targeting PD-L2, clone 3.2.B8 can be used to block this interaction, potentially relieving T cell suppression and enhancing anti-tumor immunity.
  • Mechanistic Studies: The antibody is used to investigate the role of PD-L2 in immune tolerance, lymphocyte clonal selection, and peripheral tolerance. It helps dissect the contributions of PD-L2 compared to PD-L1 in various immunological settings.
  • Preclinical Models: Similar to anti-PD-L1 therapies (which have been developed into clinically approved drugs), anti-PD-L2 antibodies like clone 3.2.B8 may be tested in mouse models of cancer, autoimmune disease, or chronic infection to assess whether PD-L2 blockade can modify disease outcomes.

Administration

While detailed in vivo protocols for clone 3.2.B8 are not specified in the available documents, in vivo functional grade antibodies are typically administered to mice via intraperitoneal (i.p.), intravenous (i.v.), or subcutaneous (s.c.) routes, depending on the experimental design. The dose, frequency, and timing are determined by the research question and pilot experiments, and may require optimization based on target engagement and off-target effects.

Experimental Readouts

In vivo studies using such antibodies commonly assess:

  • Tumor growth kinetics in syngeneic or genetically engineered mouse models of cancer.
  • Immune cell infiltration and activation in tumors or affected tissues, measured by flow cytometry or immunohistochemistry.
  • Cytokine profiles and other biomarkers of immune response modulation.
  • Survival benefits or changes in disease severity.

Key Considerations

  • Specificity: Clone 3.2.B8 binds both mouse and human PD-L2, but in vivo mouse studies use the antibody to target the endogenous mouse protein.
  • Isotype: It is a mouse IgG1 antibody, which may trigger antibody-dependent cellular cytotoxicity (ADCC) or complement-dependent cytotoxicity (CDC) via Fc receptors in vivo. The impact of this effector function should be considered in experimental design.
  • Controls: Appropriate isotype control antibodies should be used to distinguish effects specific to PD-L2 blockade from non-specific IgG effects.

Summary Table

FeatureDetails for Clone 3.2.B8 In Vivo Use
TargetMouse (and human) PD-L2 (CD273)
ApplicationImmune checkpoint blockade in mouse models
Antibody ClassMouse IgG1
Functional GradeGOLD™/PLATINUM™ (low endotoxin, in vivo ready)
PurposeMechanistic and therapeutic preclinical studies
AdministrationTypically i.p., i.v., or s.c. (protocol-dependent)
ReadoutsTumor growth, immune profiling, survival

Conclusion

Clone 3.2.B8 is used in in vivo mouse studies primarily to block PD-L2, thereby investigating the role of this immune checkpoint molecule in immune regulation and disease models, especially cancer. Its cross-reactivity with human PD-L2 also makes it valuable for translational research, though in vivo studies focus on modulating the mouse immune system. Experimental design should carefully consider the antibody’s isotype, administration route, and appropriate controls to ensure interpretable results.

I don't have specific information available about the storage temperature requirements for "sterile packaged clone 3.2.B8." The search results provided contain general storage guidelines for various medical and pharmaceutical products, but none specifically reference this particular clone designation.

The search results include storage information for COVID-19 vaccines, sterilization bags, and other sterile medical products, but without knowing the specific nature, manufacturer, or product category of clone 3.2.B8, I cannot determine its correct storage temperature requirements.

To find the accurate storage temperature for this specific product, you would need to:

  • Check the product's official labeling or packaging insert
  • Consult the manufacturer's specifications or technical documentation
  • Review any applicable regulatory guidelines for the product category
  • Contact the manufacturer or supplier directly

Storage temperatures for sterile medical products can vary significantly depending on the product type, formulation, and intended use, so it's essential to reference the specific product documentation rather than general guidelines.

Commonly used antibodies or proteins with 3.2.B8 usually depend on the research application and the precise target of this antibody, which is most often related to HLA class I antigens—specifically, the HLA-B8 allele, a well-characterized human MHC class I molecule. In the typical immunology or transplantation literature, 3.2.B8 is used for HLA typing, cell selection, functional assays, or transplantation research.

Antibodies and proteins commonly used in combination with 3.2.B8 include:

  • Other HLA class I antibodies: Researchers routinely pair 3.2.B8 with antibodies against other HLA class I alleles (e.g., HLA-A, HLA-B, HLA-C) for comparative or multiplexed HLA typing, crossmatching, or flow cytometry panels.
  • Antibodies against HLA class II molecules: In studies assessing immune compatibility or immune responses, antibodies for HLA-DR, HLA-DQ, and HLA-DP are frequently used together with HLA-B8.
  • Detection antibodies for IgG subclasses: In antibody subclass analysis (such as in Luminex or ELISA systems for transplantation immunology), subclass-specific detection antibodies (for IgG1, IgG2, IgG3, IgG4) are often used to determine the isotype of anti-HLA antibodies detected by 3.2.B8.
  • Antibodies against lineage or cell marker proteins: Commonly, researchers include antibodies for CD3, CD14, CD19, CD56, etc., to characterize or exclude specific cell types during flow cytometry of PBMC or tissue samples.
  • Fusion proteins or reference control antibodies: While not always immunologically relevant, fusion proteins may be used as positive controls or to stabilize antigens in some multiplexed assays.

Use case examples:

  • In flow cytometry: 3.2.B8 (anti-HLA-B8) might be combined with anti-CD3 (to mark T cells), anti-CD14 (monocytes), or anti-CD19 (B cells) to assess HLA expression on different cell populations.
  • In transplantation assays: 3.2.B8 is used with other anti-HLA-specific monoclonal antibodies to detect donor-specific antibodies in patient sera.

Summary Table:

Common Target Used with 3.2.B8Purpose
HLA-A, HLA-B, HLA-CHLA typing, crossmatch, immunophenotyping
HLA-DR, HLA-DQ, HLA-DPClass II typing, immune compatibility
CD3, CD14, CD19, CD56Cell-type identification, flow cytometry
IgG subclass detectionIsotype characterization, ELISA/Luminex
Fusion/reference proteinsControls, assay standardization

If you are looking for specific antibody clones or commercial reagents often used with 3.2.B8, catalogs such as Biocompare or product datasheets often list typical panels and combinations. If you meant a different "B8" antibody (such as anti-SerpinB8, ABCB8, etc.), please specify the precise system or application for a more targeted answer.

Based on the search results provided, I was not able to find specific information about "clone 3.2.B8" citations in the scientific literature. The search results primarily contain research about HIV-specific CD8+ T-cell clones and clonotypic analysis, as well as some references to heat shock proteins, but none specifically mention or discuss clone 3.2.B8.

The search results do contain valuable information about T-cell clone research methodology and findings, including studies on HIV-specific cytotoxic T-lymphocyte clones and their clonotypic composition, but these appear to be unrelated to the specific clone 3.2.B8 you're asking about.

Without relevant search results containing information about clone 3.2.B8, I cannot provide the key findings from its citations in scientific literature. To get accurate information about this specific clone, you would need search results that specifically reference clone 3.2.B8 or related research.

References & Citations

1.) Akbari O, Stock P, Singh AK, Lombardi V, Lee WL, Freeman GJ, Sharpe AH, Umetsu DT, Dekruyff RH. PD-L1 and PD-L2 modulate airway inflammation and iNKT-cell- dependent airway hyperreactivity in opposing directions. Mucosal Immunol. 2010; 3:81- 91. PMCID: PMC2845714
2.) . Xiao Y, Yu S, Zhu B, Bedoret D, Bu X, Francisco LM, Hua P, Duke-Cohan JS, Umetsu DT, Sharpe AH, DeKruyff RH*, Freeman GJ* (* indicates co-senior authors). RGMb is a novel binding partner for PD-L2 and its engagement with PD-L2 promotes respiratory tolerance. J Exp Med. 2014; 211:943-59. PMCID: PMC4010901.
B
Flow Cytometry
in vivo Protocol
General Western Blot Protocol

Certificate of Analysis

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Formats Available

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