CTLA4 : B7-2[Biotinylated] Inhibitor Screening Assay Kit

Catalog #
79658
$1,205 *
Size: 96 reactions
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Description

The CTLA4:B7-2[Biotinylated] Inhibitor Screening Assay Kit is designed for screening and profiling inhibitors of CTLA4:B7-2-biotin interaction. The key to this kit is the high sensitivity of detection of CTLA4 by streptavidin-HRP. Only a few simple steps on a microtiter plate are required for the assay. First, CTLA4 is coated on a 96-well plate. Next, B7-2-biotin is incubated with CTLA4 on the plate. Finally, the plate is treated with streptavidin-HRP followed by addition of an HRP substrate to produce chemiluminescence, which can then be measured using a chemiluminescence reader.

This product has been cited 1 time.

Synonyms
Cytotoxic T-lymphocyte-associated protein 4 CD152, T-lymphocyte activation antigen CD86, B7.2, FUN-1, B70, BU63, CD86, B72, CTLA-4
Product Info
Storage and Usage
Citations1
Assay Kit Format
Chemiluminescent
Supplied As
This kit comes in a convenient 96-well format, with CTLA4 (CD152), purified biotin-labeled B7-2 (CD86), streptavidin-labeled HRP, and assay buffer for 100 binding reactions.
Format
Catalog # Component Amount Storage
71149 CTLA4 (CD152), Fc-tag 10 µg -80°C

(Avoid freeze/ thaw cycles!)

71159 B7-2 (CD86), Fc-Biotin-labeled 3 µg -80°C
79742 Streptavidin-HRP 10 µl +4°C
79311 3x Immuno Buffer 1 50 ml -20°C
79728 Blocking Buffer 2 50 ml +4°C
  HRP chemiluminescent substrate A (transparent bottle) 6 ml +4°C
  HRP chemiluminescent substrate B (brown bottle) 6 ml +4°C
79699 White 96-well microplate 1 +4°C
UniProt #
CTLA4: P16410; B7-2: P42081
Background
B7-2 (CD86) signaling through CTLA4 (CD152) has been shown to inhibit T- cell activation. This co-inhibitory pathway can be overactive in many tumors, enabling cancers to escape the host’s immune system. CTLA4-blocking antibodies, including Ipilimumab (Yervoy) and Tremelimumab, have shown clinical efficacy in treating cancer.
References

1. Ohtani, H., et al., Lab Invest. 1997; 77(3): 231-241.
2. Robert, C., et al., N. Engl. J. Med. 2011; 364: 2517-2526.