Anti-Mouse CD2 Antibody

Product Details


CloneRM2-5
ApplicationFlow Cytometry, IP, Costimulation, Block
ReactivityMouse
FormatPurified
Target NameCD2, LFA-2, T11, Ly-37, SRBC-R
IsotypeRat IgG2b
Antibody TypeMonoclonal
Regulatory StatusRUO
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide
Protein Concentration0.5 mg/mL
Storage & HandlingThe antibody solution should be stored between 2°C and 8°C
Recommended UsageFor flow cytometric staining, it is recommended to use less than 0.2 µg of this reagent per 0.5-1.0 million cells in a 100 µL volume. Optimal reagent performance should be determined by titration for each specific application
See All FormatsClone RM2-5

Background Information


Mouse CD2 is a cell surface glycoprotein of the immunoglobulin superfamily expressed primarily on T lymphocytes, natural killer (NK) cells, and a subset of thymocytes. It functions as an adhesion and costimulatory receptor that promotes stable interactions between immune cells, facilitating antigen recognition, immune synapse formation, and lymphocyte activation. CD2 lowers the threshold for T-cell receptor (TCR) signaling by strengthening contact between T cells and antigen-presenting cells (APCs), thereby enhancing T-cell proliferation, cytokine production, and cytotoxic effector functions. In NK cells, CD2 similarly augments activation and target cell killing through cooperative signaling with other activating receptors.

Structurally, mouse CD2 is a type I transmembrane glycoprotein consisting of two extracellular immunoglobulin-like domains, a single transmembrane region, and a relatively long cytoplasmic tail that lacks intrinsic enzymatic activity but interacts with intracellular adaptor proteins involved in cytoskeletal organization and signal transduction. Unlike human CD2, whose principal ligand is CD58 (LFA-3), mouse CD2 binds primarily to CD48, another immunoglobulin superfamily member expressed on hematopoietic cells. The CD2-CD48 interaction mediates cell adhesion and promotes efficient communication between T cells, NK cells, B cells, dendritic cells, and macrophages during immune responses.

Mouse CD2 plays an important role in adaptive and innate immunity, and alterations in CD2-mediated signaling have been associated with impaired immune responses, autoimmunity, transplantation immunity, and inflammatory disease in experimental models. CD2-deficient mice exhibit defects in T-cell activation and reduced efficiency of immune synapse formation, although compensatory pathways often preserve overall immune function. Because of its restricted expression on lymphocytes, CD2 is widely used as a marker for T cells and NK cells in immunological research. Therapeutically, CD2 has been investigated as a target for modulating T-cell activation in autoimmune disease, transplantation, and inflammatory disorders. In mouse models, antibodies directed against CD2 have been used experimentally to deplete or regulate T cells, while CD2-targeted approaches continue to serve as valuable tools for studying immune regulation and evaluating novel immunotherapies.

Isotype Control


Rat IgG2b Isotype Control

Data Sheets


Anti-Mouse CD2 Antibody TDS

Related Protocols


Flow Cytometry Protocol

Frequently Asked Questions


How do I determine the optimal antibody concentration/titer for my experiment?
We recommend titrating each new antibody lot on your own cell type and instrument, since optimal concentration depends on cell density, target expression level, and cytometer sensitivity. Suggested starting dilutions or test sizes (e.g., µg or µl per 10^6 cells) are provided on the product page as a starting reference point, not a fixed requirement.

Can these antibodies be used for intracellular or intranuclear staining, or only surface staining?
Intended use (surface, intracellular, or both) is specified per product, indicated under Application. The appropriate Related Protocol is linked for each product. If you need to detect both surface and intracellular markers in the same panel, confirm each antibody's compatibility with your fixation/permeabilization protocol before combining them.

What controls should I use alongside these antibodies?
Matched isotype controls (same host species, isotype, and conjugate) are available for most clones to help distinguish specific binding from background/non-specific staining and are linked on each product page. Unstained, single-color compensation, and fluorescence-minus-one (FMO) controls are also recommended, especially for multicolor panel design.

Can I combine InnoCyto Flow Cytometry antibodies into a multicolor panel?
Yes — antibodies across our catalog are designed to be panel-compatible, and conjugate options are offered specifically to support multiplexing. When building a panel, pair bright fluorophores with low-expression targets, avoid excessive spectral overlap, and confirm compensation is set up correctly for your specific fluorochrome combination. Use our Panel Builder to simplify the process.

Have a product or application question? Consult our FAQs or contact us.