Flow cytometric analysis of SD Rat splenocytes treated 4h with 10μg/ml LPS (Right) or untreated (Left) labeling CD86 at 1/2000 dilution (0.1 μg). Goat Anti - Mouse IgG Alexa Fluor® 488 was used as the secondary antibody. Then cells were stained with CD45RA - Allophycocyanin separately. Gated on total viable cells.
Product Details
Product Details
Product Specification
Host | Mouse |
Antigen | CD86 |
Location | Cell membrane |
Accession | A6IRC2 |
Clone Number | S-R580 |
Antibody Type | Mouse mAb |
Isotype | IgG1,k |
Application | FCM |
Reactivity | Rt |
Positive Sample | SD Rat splenocytes treated 4h with 10μg/ml LPS |
Purification | Protein G |
Concentration | 2 mg/ml |
Conjugation | Unconjugated |
Physical Appearance | Liquid |
Storage Buffer | PBS pH7.4 |
Stability & Storage | 12 months from date of receipt / reconstitution, 2 to 8 °C as supplied. |
Dilution
application | dilution | species |
FCM | 1:2000 | Rt |
Background
CD86, also known as B7-2, is a 70 kDa glycoprotein and a type I membrane protein that belongs to the immunoglobulin superfamily. It is primarily expressed on antigen-presenting cells (APCs) such as dendritic cells, macrophages, and B cells. CD86 serves as a ligand for two T cell surface proteins: CD28 and CTLA-4. The interaction between CD86 and CD28 provides a crucial co-stimulatory signal for T cell activation and survival, while binding to CTLA-4 negatively regulates T cell activation, thereby dampening the immune response. Additionally, CD86 plays a role in B cell function regulation and can influence IgG1 production. It is rapidly upregulated on B cells upon activation and can be induced on monocytes by interferon-gamma. CD86 is also involved in various immune processes, including the activation of the NF-kappa-B signaling pathway and the regulation of cytokine production.
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