Cat. No. HS-466 003 |
50 µg specific antibody, lyophilized. Affinity purified with the immunogen. Albumin and azide were added for stabilization. For reconstitution add 50 µl H2O to get a 1mg/ml solution in PBS. Then aliquot and store at -20°C to -80°C until use. Antibodies should be stored at +4°C when still lyophilized. Do not freeze! |
Applications |
Immunoprecipitation (IP); Immunoisolation or pulldown of a target molecule using an antibody. For details and product specific hints, please refer to the ”Remarks” section.', $event)" style="cursor: help;">IP: not tested yet Immunocytochemistry (ICC) on 4% PFA fixed cells. Immunoreactivity is usually revealed by fluorescence. Some antibodies require special fixation methods. For details, please refer to the “Remarks” section.', $event)" style="cursor: help;">ICC: not tested yet Immunohistochemistry (IHC) on 4% PFA perfusion fixed tissue with 24h PFA post fixation. Immunoreactivity is usually revealed by fluorescence or a chromogenic substrate. Some antibodies require special fixation methods or antigen retrieval steps. For details, please refer to the ”Remarks” section.', $event)" style="cursor: help;">IHC: 1 : 500 (see remarks) gallery Immunohistochemistry (IHC-P) of formalin fixed, paraffin embedded (FFPE) tissue (some antibodies require special antigen retrieval steps, please refer to the ”Remarks” section). Immunoreactivity is usually revealed by fluorescence or a chromogenic substrate.', $event)" style="cursor: help;">IHC-P: 1 : 400 gallery |
Immunogen | Synthetic peptide corresponding to AA 291 to 309 from mouse Cd86 (UniProt Id: P42082) |
Reactivity |
Reacts with: mouse (P42082). No signal: human (P42081), rat. Other species not tested yet. |
Remarks |
IHC: Heat-mediated antigen retrieval (in citrate buffer pH 6) is required for immunohistochemical staining of PFA fixed tissues. Methanol fixation is required for immunohistochemical staining of fresh frozen tissues. |
Data sheet | hs-466_003.pdf |
CD86 (Cluster of Differentiation 86, also known as B7.2) belongs to the B7 family of immune-regulatory cell-surface protein ligands (1). CD86 and the genetically closely linked CD80 protein (also known as B7.1) are expressed by antigen presenting cells and provide costimulatory signals necessary for T cell activation and tolerance via interaction with CD28 and cytotoxic T-lymphocyte antigen 4 (CTLA-4) expressed on T-cells. However, CD80 and CD86 have non-equivalent roles in immune modulation: CD86 is the dominant ligand for proliferation and survival of regulatory T cells (Tregs) (2) and shows in comparison with CD80 very high efficiency at increasing T cell killing capacity (3). CD86 is expressed only at low levels on resting B cells, dendritic cells and macrophages; activation results in enhanced CD86 expression (Collins et al., 2005). In the CNS, CD86 upregulation is a marker of activated pro-inflammatory M1 microglia (4). In oncology research, CD86 is a biomarker to phenotypically differentiate classically activated M1 macrophages from alternatively activated M2 macrophages in the tumor microenvironment (5).