Anti-mouse Tim-4 Antibody

Product Details


CloneRMT4-54
ApplicationFlow Cytometry
ReactivityMouse
FormatPurified
Target NameTim-4, Tim4, T cell immunoglobulin and mucin domain containing protein-4
IsotypeRat IgG2a
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 RMT4-54

Background Information


Mouse TIM-4 (T-cell immunoglobulin and mucin-domain containing protein 4), encoded by the Havcr2 gene, is a cell-surface immunoregulatory protein expressed primarily on antigen-presenting cells, including macrophages and dendritic cells. TIM-4 plays an important role in the recognition and clearance of apoptotic cells and in the regulation of immune responses. By binding phosphatidylserine exposed on the surface of apoptotic cells, TIM-4 helps phagocytic cells identify and remove dying cells, thereby contributing to tissue homeostasis and limiting the persistence of cellular debris and inflammatory signals.



Mouse TIM-4 is a type I transmembrane glycoprotein belonging to the TIM family. Its extracellular region contains an immunoglobulin-like V-type domain followed by a mucin-like domain, a transmembrane region, and a cytoplasmic tail. Unlike several other TIM family members, TIM-4 lacks a conventional intracellular signaling motif and primarily functions as a ligand-binding and cell-interaction molecule. Its best-characterized ligand is phosphatidylserine (PtdSer), which becomes exposed on the outer leaflet of the plasma membrane during apoptosis. TIM-4 can also participate in interactions with other immune-cell molecules, including pathways involving TIM-1.



Abnormal TIM-4-mediated recognition of apoptotic cells has been implicated in autoimmune and inflammatory diseases. Efficient clearance of apoptotic cells is important for preventing the accumulation of cellular material that can stimulate inappropriate immune responses. TIM-4 expression and function have been investigated in experimental models of autoimmune disease, allergy, transplantation, and tumor immunity. Depending on the cellular and disease context, TIM-4-mediated interactions can either promote immune tolerance or influence inflammatory responses.



Because TIM-4 participates in apoptotic-cell clearance and immune regulation, it is being investigated as a potential therapeutic target. Modulating TIM-4 activity may influence macrophage-mediated clearance, immune tolerance, and inflammatory responses. Experimental approaches targeting the TIM-4 pathway have been explored in autoimmune disease, transplantation, and cancer research. Mouse TIM-4 is therefore also an important research tool for studying phagocytosis, immune regulation, and mechanisms controlling the response to apoptotic cells.

Isotype Control


Rat IgG2a Isotype Control Antibody

Data Sheets


Anti-mouse Tim-4 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.