CD28:B7-2[Biotinylated] Inhibitor Screening Assay Kit

Catalog #
72062
$1,070 *
Size: 96 reactions
Qty
*US Pricing only. For international pricing, please contact your local distributor.
Purchase
Description

The CD28:B7-2[Biotinylated] Inhibitor Screening Assay Kit is designed for screening and profiling inhibitors of CD28:B7-2 signaling. The key to this kit is the high sensitivity of detection of biotin-labeled B7-2 by streptavidin-HRP. Only a few simple steps on a microtiter plate are required for the assay. First, CD28 is coated on a 96-well plate. Next, B7-2 is incubated with CD28 on the plate. Finally, the plate is treated with streptavidin-HRP followed by addition of an HRP substrate to produce chemiluminescence, which can be measured using a chemiluminescence reader.

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Synonyms
T-Cell-Specific Surface Glycoprotein, TP44, T-lymphocyte activation antigen CD86, B7.2, FUN-1, B70, BU63, CD86, B72
Product Info
Storage and Usage
Citations
Assay Kit Format
Chemiluminescent
Supplied As
This kit comes in a convenient 96-well format, with biotin-labeled B7-2, purified CD28, streptavidin-labeled HRP, and assay buffer for 100 binding reactions.
Format
Catalog
Number 

Component

Amount

Storage
71159 B7-2, Biotin-labeled 20 µg -80 °C

Avoid multiple
freeze/thaw 
cycles
71113 CD28 20 µg -80 °C
79311 3x Immuno Buffer 1 50 ml -20 °C
Blocking Buffer 50 ml +4 °C
Streptavidin-HRP 15 µl -20 °C
HRP chemiluminescent substrate A
(transparent bottle)
6 ml +4 °C
HRP chemiluminescent substrate B
(brown bottle)
6 ml +4 °C
96-well white microplate 1 +4 °C
UniProt #
CD28: P10747; B7-2: P42081
Background
The activation of naïve T cells requires two signals; the specific T cell receptor recognition of MHC/Antigen on the surface of the antigen-presenting cell (APC), and the binding of B7-2 (CD86) ligand on the APC with the CD28 receptor on the T cell surface. CD28:B7-2 interaction is an important drug target for the regulation of T cells involved in autoimmunity, inflammation, tumor recognition, and immune tolerance.
References
1. Keir, M.E., et al. Immunol. Rev. 2005, 204: 128-143.

2. Yao, S., et al. Immunity 2011, 34(5):729-40.