APC/Cyanine7 Anti-Human CD86 Antibody

Product Details


CloneIT2.2
ApplicationFlow Cytometry
ReactivityHuman
FormatAPC/Cyanine7
Target NameCD86, B7-2, B70
IsotypeMouse IgG2b
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 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. APC/Cyanine7 has an excitation max at 650 nm and an emission max at 774 nm.
Excitation LaserRed Laser (633 nm)
See All FormatsClone IT2.2

Background Information


Human CD86, also known as B7-2, is a type I transmembrane glycoprotein and a key costimulatory molecule expressed primarily on professional antigen-presenting cells (APCs), including dendritic cells, macrophages, and B cells. Encoded by the CD86 gene, CD86 is rapidly upregulated following immune activation and plays an essential role in regulating adaptive immune responses. Its primary function is to provide the second signal required for full T-cell activation, proliferation, and cytokine production after antigen recognition by the T-cell receptor.



CD86 belongs to the immunoglobulin (Ig) superfamily and consists of two extracellular Ig-like domains, a single transmembrane domain, and a short cytoplasmic tail. The principal ligands for CD86 are CD28 and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), both expressed on T cells. Binding of CD86 to CD28 delivers a positive costimulatory signal that promotes T-cell activation and survival, whereas interaction with CTLA-4 transmits an inhibitory signal that suppresses immune responses and helps maintain peripheral tolerance. The balance between these receptor interactions is critical for immune homeostasis.



Aberrant CD86 expression has been implicated in numerous diseases, including autoimmune disorders such as rheumatoid arthritis, systemic lupus erythematosus, and multiple sclerosis, where excessive costimulation contributes to pathogenic T-cell activation. Increased CD86 expression has also been observed in chronic inflammatory conditions and certain hematologic and solid malignancies, where it may influence antitumor immunity or immune evasion.



CD86 is an important therapeutic target for immune modulation. CTLA-4-Ig fusion proteins, including abatacept and belatacept, bind CD86 (and CD80) to block CD28-mediated costimulation, thereby suppressing T-cell activation. These agents are approved for the treatment of autoimmune diseases and prevention of transplant rejection. Ongoing research is evaluating additional therapeutic strategies targeting the CD80/CD86 pathway to enhance cancer immunotherapy, promote transplantation tolerance, and treat autoimmune and inflammatory diseases.

Isotype Control


APC/Cyanine7 Mouse IgG2b Isotype Control

Data Sheets


APC/Cyanine7 Anti-Human 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.