Anti-Mouse CD155 (PVR) [Clone 4.24.1] — Purified in vivo GOLD™ Functional Grade

Anti-Mouse CD155 (PVR) [Clone 4.24.1] — Purified in vivo GOLD™ Functional Grade

Product No.: C2833

[product_table name="All Top" skus="C2833"]

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Clone
4.24.1
Target
CD155
Formats AvailableView All
Product Type
Monoclonal Antibody
Alternate Names
PVR (poliovirus receptor) homolog, Clone 4.24
Isotype
Rat IgG2a κ
Applications
B
,
FC
,
in vivo

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Antibody Details

Product Details

Reactive Species
Mouse
Host Species
Rat
Recommended Isotype Controls
Recommended Dilution Buffer
Immunogen
EL4 transfected with mouse CD155
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.
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.
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
FC The suggested concentration for this 4.24.1 antibody for staining cells in flow cytometry is ≤ 0.25 μg per 106 cells in a volume of 100 μl. Titration of the reagent is recommended for optimal performance for each application.
Additional Applications Reported In Literature ?
B
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 4.24.1 recognizes an epitope on mouse CD155.
Background
CD155 is a transmembrane glycoprotein member of a subfamily of immunoglobulin-like adhesion receptors (nectins). CD155 is commonly known as Poliovirus Receptor (PVR) because of its involvement as a cellular receptor for poliovirus. The normal function of CD155 is to establish intercellular adherens junctions between epithelial cells. Of its 3 extracellular immunoglobulin-like domains (D1, D2, and D3), the virus only recognizes D1. CD155 interacts with both CD226 and CD96 to induce cytotoxicity of NK cells and CTL. The precise role of CD155 in the immune system remains to be elucidated, though it is suspected to be involved in intestinal humoral immune responses. Furthermore, it is thought that CD155 may be used to positively select MHC-independent T cells in the thymus.
Antigen Distribution
CD155 is expressed at cell junctions on the primary vascular endothelial cells and is highly expressed on DP thymocytes.
Ligand/Receptor
CD226 (DNAM-1), CD96
Function
Apart from its function of adhering junction among contacting epithelial cells, the interaction of DNAM-1 (CD226) with its ligands CD155 and CD112 (nectin 2) induces cytotoxcity of NK cells and CD8+ T cells and cytokine secretion.
NCBI Gene Bank ID
Research Area
Immunology
.
Innate Immunity

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 4.24.1 is a monoclonal antibody specific for mouse CD155 (also known as PVR) and is commonly used in in vivo mouse studies to functionally target or detect CD155-expressing cells. In these studies, clone 4.24.1 serves as a tool for investigating the role of CD155 in immune modulation, tumor immunology, or cellular interactions.

Key details about its in vivo use:

  • Antibody type: It is produced in an in vivo functional grade suitable for in vivo studies, indicating low endotoxin levels and compatibility with systemic injection into mice.
  • Applications: Researchers employ clone 4.24.1 for:
    • Functional blockade or modulation of CD155-mediated pathways in living mice (for example, to analyze immune cell engagement, tumor immunity, or receptor-ligand interactions between CD155 and immune effectors).
    • Depletion or labeling of CD155+ cells to study their role in various physiological or pathological contexts.
    • Mechanistic studies: Used in experiments such as blocking assays, immune profiling, and examining CD155's role in tumor growth or immune escape.

Typical in vivo procedures may involve:

  • Systemic (intravenous or intraperitoneal) injection of clone 4.24.1 in mouse models, sometimes in combination with other agents, to analyze how CD155 affects outcomes like tumor progression, immune cell migration, or cytotoxic responses.
  • Functional assays or immune phenotyping following treatment, to measure changes in cell populations, cytokine responses, or disease parameters.

Supporting details:

  • Clone 4.24.1 is validated for in vivo use and is available as a low endotoxin, functional-grade reagent from several suppliers, indicating widespread application in experimental immunology and oncology.
  • CD155 expression is prominent at cell junctions in primary vascular endothelial cells, as well as on certain tumor and immune cells—making clone 4.24.1 of particular interest in tumor immunology.

Overall, clone 4.24.1 is an established antibody for specifically targeting mouse CD155 in vivo, enabling diverse functional, mechanistic, and depletion studies within immunology and oncology research contexts.

Several antibodies and proteins are commonly used alongside 4.24.1 (a 4-1BB agonist antibody) in the literature, particularly in the context of cancer immunotherapy and studies involving immune cell modulation.

In research focused on 4-1BB targeting, bispecific antibodies are a leading strategy. These antibodies are engineered to bind both 4-1BB and another target protein—often a tumor-associated or immune regulation antigen. The most frequently paired targets include:

  • Her2 (human epidermal growth factor receptor 2): Used for selectively directing 4-1BB agonism to Her2-positive tumor cells.
  • PD-L1 (Programmed death-ligand 1): Combining 4-1BB activation with PD-L1 blockade aims to simultaneously enhance T cell activity and block immunosuppression in the tumor microenvironment.
  • FAP (fibroblast activation protein): Targeting FAP, frequently expressed in tumor stroma, can help localize 4-1BB agonist action within the tumor.

Other proteins and antibodies commonly associated in these studies include:

  • Urelumab (BMS-663513) and Utomilumab (PF-05082566): First-generation monospecific clinical 4-1BB agonists, though their utility has been limited by toxicity or lack of efficacy.
  • PM1003: A bispecific nanobody combining 4-1BB agonism with PD-L1 engagement, noted for pronounced tumor activity and reduced toxicity.

In addition, studies frequently utilize general immunoassay antibodies for phenotypic characterization, such as anti-CD3, anti-CD8, anti-PD-1, and anti-Her2, depending on the co-target being investigated.

Summary Table: Commonly Paired Antibodies/Proteins with 4-1BB Agonists (like 4.24.1)

Co-target Protein/AntibodyReason for Pairing with 4-1BB
Her2Direct 4-1BB agonism to Her2+ tumors—enhanced specificity
PD-L1Block immunosuppression, boost T cell response
FAPLocalize action to tumor stroma, reduce off-target effects
Urelumab, UtomilumabBenchmark clinical comparators for 4-1BB activation
PM1003Clinical bispecific; high efficacy, low toxicity in trials

Many studies also employ antibodies targeting T cell markers and checkpoint proteins when profiling immune cells, but Her2, PD-L1, and FAP remain the most prominent in bispecific formats for therapeutic development with 4-1BB agonists.

If you have a specific experimental context (e.g., immunofluorescence, flow cytometry, or therapeutic applications), please clarify for more tailored recommendations.

Current search results do not identify any scientific literature, publications, or key findings specifically associated with "clone 4.24.1" or its citations. There are no matches for "clone 4.24.1" within provided databases, review guides, or discussions of citation practices.

Key Context from Search Results:

  • The importance of accurate citation practice and prevalence of citation inaccuracy is discussed in biomedical literature. However, these results are general and not related to "clone 4.24.1."
  • Evaluation of AI tools for literature reviews highlights that fabricated or incorrect citations are a problem, but no mention is made of "clone 4.24.1".
  • Critical analysis of literature is vital for scientific rigor, but the name or phrase in your query is not addressed in any guidance or example.

Possible Explanations:

  • It is possible "clone 4.24.1" refers to a highly specific research tool, software module, plasmid, antibody, or biological clone that is not broadly cited or is so new/obscure that it does not appear in indexed literature.
  • There may be a misidentification or typographical error in the query, or the topic might require searching specialized databases or proprietary research archives.

If you provide additional context—such as the field of research, species, or application—I can refine the search and provide more targeted information if available. As of now, there are no documented key findings linked to "clone 4.24.1" citations in scientific literature according to current sources.

Dosing regimens for clone 4.24.1 are not detailed in the provided search results; standard guidance summarizes dosing for more commonly used clones (such as anti-CTLA-4 clones 9H10 or 9D9, anti-CD4 GK1.5, and anti-CD8 2.43) in various mouse models. No direct mention or dosing schedule for clone 4.24.1 is given, suggesting limited publicly available data or that this clone is less widely used or reported in peer-reviewed protocols.

General guidelines from related antibody dosing in mouse models:

  • Typical doses for immune-modulating or depleting antibodies range from 100–250 ?g per mouse, administered intraperitoneally.
  • Dosing schedules commonly use 2–3 times per week, or every 3 days, depending on the antibody mechanism and study purpose.

Variation across mouse models:

  • Dosing can be model-dependent, varying by mouse strain, tumor model, immune status, and experimental aim.
  • For example, protocols for checkpoint inhibitors recommend not exceeding 200 ?g per dose to avoid toxicity, with modifications for sensitive strains or combination therapies.
  • Pharmacokinetics and pharmacodynamics assessments may sometimes support changing dose frequency, but inter-strain differences do not always justify major dose adjustments.

In summary, without clone-specific data for 4.24.1, use the standard extrapolation of 100–250 ?g per mouse intraperitoneally every 3 days as a starting point—then optimize based on pilot studies and published protocols for functionally similar antibodies. If your application is novel or high-risk, consult directly with suppliers or recent publications for any available updates, and always validate efficacy and safety in your specific model.

References & Citations

1. Kourepini, E. et al. (2016) J. Immunol. 196(9):3570-3580.
B
Flow Cytometry
in vivo 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.