iF647 Anti-Mouse CD134 (OX-40) Antibody

Product Details


CloneOX-86
ApplicationFlow Cytometry
ReactivityMouse
FormatiF647
Target NameCD134, OX-40, OX40, TNFRSF4, ACT35
IsotypeRat IgG1
Antibody TypeMonoclonal
Regulatory StatusRUO
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and 0.2% (w/v) BSA
Protein Concentration0.2 mg/mL
Storage & HandlingThe antibody solution should be stored undiluted between 2°C and 8°C, and protected from prolonged exposure to light. Do not freeze.
Recommended UsageFor flow cytometric staining, it is recommended to use 5 µL 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. iF647 has an excitation max at 656 nm and an emission max at 670 nm.
Excitation LaserRed Laser (633 nm)
See All FormatsClone OX-86

Background Information


Mouse CD134, also known as OX40 or TNFRSF4, is a member of the tumor necrosis factor receptor (TNFR) superfamily and an important costimulatory receptor on T cells. OX40 is induced following T-cell receptor activation and is expressed predominantly on activated CD4+ and CD8+ T cells. In mice, OX40 is also constitutively expressed on certain regulatory T cells (Tregs). OX40 signaling promotes T-cell proliferation, survival, differentiation, cytokine production, and formation of memory T cells, thereby strengthening and sustaining antigen-specific immune responses.



Mouse OX40 is a type I transmembrane glycoprotein belonging to the TNFR superfamily. It contains an extracellular region with characteristic cysteine-rich domains, a single transmembrane segment, and a cytoplasmic signaling tail. The principal and currently established ligand is OX40 ligand (OX40L), also known as CD252 or TNFSF4. OX40L is a type II transmembrane TNF-superfamily protein expressed primarily by activated antigen-presenting cells, including dendritic cells, macrophages, and B cells. OX40L forms a trimer and engages OX40 to initiate downstream signaling through pathways including NF-κB and PI3K/Akt.



Excessive OX40 signaling can contribute to chronic inflammation and autoimmune disease. In mouse models, the OX40–OX40L pathway has been implicated in experimental autoimmune encephalomyelitis, asthma, colitis, diabetes, arthritis, graft-versus-host disease, and transplant rejection. Blocking OX40 or OX40L can substantially reduce disease severity in several of these models, supporting the pathway as a potential therapeutic target.



Therapeutically, OX40 can be targeted in two opposing ways. Agonistic anti-OX40 antibodies or OX40L-based agonists can enhance T-cell activation and antitumor immunity, making OX40 an attractive target for cancer immunotherapy and vaccine development. Conversely, antagonistic antibodies or OX40L blockade may suppress pathogenic T-cell responses in autoimmune and inflammatory diseases. OX40 agonists, including combinations with immune-checkpoint inhibitors, continue to be investigated clinically, although antitumor efficacy has so far been variable.

Isotype Control


iF647 Rat IgG1 Isotype Control Antibody

Data Sheets


iF647 Anti-Mouse CD134 (OX-40) 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.