Data & Images
|Product Name||Anti-CD86/B7-2 Antibody|
|Description||Rabbit IgG polyclonal antibody for T-lymphocyte activation antigen CD86(CD86) detection. Tested with WB in Mouse.|
|Cite This Product||Anti-CD86/B7-2 Antibody (Boster Biological Technology, Pleasanton CA, USA, Catalog # PA1394)|
|Replacement Item||This antibody may replace the following items: sc-1635|sc-1636|sc-19617|sc-28347|sc-58915|sc-9092 from Santa Cruz Biotechnology.|
*Our Boster Guarantee covers the use of this product in the above tested applications.
**For positive and negative control design, consult "Tissue specificity" under Protein Target Info.
|Recommended Detection Systems||Boster recommends Enhanced Chemiluminescent Kit with anti-Rabbit IgG (EK1002) for Western blot.
*Blocking peptide can be purchased at $50. Contact us for more information
**Boster also offers various secondary antibodies for Immunoflourescecne and IHC. Take advantage of the buy 1 primary antibody get 1 secondary antibody for free promotion for the entire year 2017!
|Immunogen||A synthetic peptide corresponding to a sequence at the N-terminus of mouse CD86(66-80aa YEHYLGTEKLDSVNA), different from the related rat sequence by two amino acids.|
|Cross Reactivity||No cross reactivity with other proteins|
|Contents||Each vial contains 5mg BSA, 0.9mg NaCl, 0.2mg Na2HPO4, 0.05mg Thimerosal, 0.05mg NaN3.
*carrier free antibody available upon request.
|Concentration||Add 0.2ml of distilled water will yield a concentration of 500ug/ml.|
|Storage||At -20˚C for one year. After reconstitution, at 4˚C for one month. It can also be aliquotted and stored frozen at -20˚C for a longer time.Avoid repeated freezing and thawing.|
|Purification||Immunogen affinity purified.|
Protein Target Info (Source: Uniprot.org)
You can check the tissue specificity below for information on selecting positive and negative control.
|Protein Name||T-lymphocyte activation antigen CD86|
|Molecular Weight||34666 MW|
|Protein Function||Receptor involved in the costimulatory signal essential for T-lymphocyte proliferation and interleukin-2 production, by binding CD28 or CTLA-4. May play a critical role in the early events of T-cell activation and costimulation of naive T-cells, such as deciding between immunity and anergy that is made by T- cells within 24 hours after activation.|
|Tissue Specificity||Expressed on activated B-cells.|
|Sequence Similarities||Contains 1 Ig-like C2-type (immunoglobulin-like) domain.|
|Subcellular Localization||Cell membrane ; Single-pass type I membrane protein .|
|Alternative Names||T-lymphocyte activation antigen CD86;Activation B7-2 antigen;Early T-cell costimulatory molecule 1;ETC-1;CD86;Cd86;|
|Research Areas|||immunology|adaptive immunity|t cells| immunology|cell type markers|non-lineage| microbiology|interspecies interaction|host virus interaction| stem cells|hematopoietic progenitors|lymphoid|b lymphocytic lineage|myeloid|dendritic cell lineage|monocytic lineage|regulatory t cells| kits/ lysates/ other|elisa kits|cd markers elisa kits||
Background for T-lymphocyte activation antigen CD86
Dilution Ratios/Recommended Concentrations
At Boster we strive to provide the best Anti-CD86/B7-2 Antibody by testing all applications on non-spiked tissues and cell lines to ensure that the affinity of the antibody is enough to react to the endogenouse level of the target protein. Read more about our QC panel here.
|Recommended dilution ratios are listed below:|
Western blot, 0.1-0.5μg/ml, Mouse|
**Boster provides high sensitivity secondary antibody kits for Western blotting and IHC. For more info see Related Products below.
Anti-CD86/B7-2 Antibody Images
Click the images to enlarge.
Lane 1: Recombinant Mouse CD86 Protein 10ng
Lane 2: Recombinant Mouse CD86 Protein 5ng
Lane 3: Recombinant Mouse CD86 Protein 2.5ng
1. Post-translational modification:phosphorylation, methylation, glycosylation etc. These modifications prevent SDS molecules from binding to the target protein and thus make the band size appear larger than expected
2. Post-translational cleavage: this can cause smaller bands and or multiple bands
3. Alternative splicing: the same gene can have alternative splicing patterns generating different size proteins, all with reactivities to the antibody.
4. Amino Acid R chain charge: SDS binds to positive charges. The different size and charge of the Amino Acid side chains can affect the amount of SDS binding and thus affect the observed band size.
5. Multimers: Multimers are usually broken up in reducing conditions. However if the interactions between the multimers are strong, the band may appear higher.,