iF647 Anti-mouse CD86 Antibody

Product Details


CloneGL-1
ApplicationFlow Cytometry
ReactivityMouse
FormatiF647
Target NameCD86, B7-2, Ly-58, B70
IsotypeRat IgG2a
Antibody TypeMonoclonal
Regulatory StatusRUO
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and 0.2% (w/v) BSA
Protein ConcentrationSupplied at a lot-specific concentration.
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 less than 0.5 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. iF647 has an excitation max at 656 nm and an emission max at 670 nm.
Excitation LaserRed Laser (633 nm)
See All FormatsClone GL-1

Background Information


Mouse CD86 (also known as B7-2) is a co-stimulatory surface protein expressed primarily on antigen-presenting cells (APCs), including dendritic cells, macrophages, and B cells. It plays a central role in T cell activation by providing the necessary second signal required for full T cell priming, complementing antigen recognition through the T cell receptor. Upon immune stimulation, CD86 expression is rapidly upregulated, enabling efficient initiation of adaptive immune responses and regulation of T cell differentiation.

Structurally, CD86 is a type I transmembrane glycoprotein and a member of the immunoglobulin superfamily. It contains extracellular IgV- and IgC-like domains responsible for ligand binding, a single-pass transmembrane region, and a short cytoplasmic tail lacking intrinsic enzymatic activity. Despite this, CD86 can participate in intracellular signaling through association with adaptor molecules and membrane microdomains, influencing APC activation and cytokine production.

The primary ligands of CD86 are CD28 and CTLA-4 (CD152), both expressed on T cells. Interaction with CD28 delivers a positive co-stimulatory signal that promotes T cell proliferation, cytokine secretion, and survival, while binding to CTLA-4 transmits inhibitory signals that dampen immune responses and maintain tolerance.

CD86 is implicated in autoimmune diseases, transplant rejection, and chronic inflammation due to dysregulated co-stimulation. It is also involved in tumor immune evasion by influencing T cell activation thresholds.

Therapeutically, the CD86 pathway is targeted by agents such as CTLA-4-Ig fusion proteins (e.g., abatacept) that block CD28-mediated co-stimulation, providing benefit in autoimmune diseases. Modulating CD86 activity also holds promise in cancer immunotherapy and transplant tolerance strategies.

Isotype Control


iF647 Rat IgG2a Isotype control

Data Sheets


iF647 Anti-mouse CD86 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.