| Product Includes | Product # | Quantity | Mol. Wt | Isotype/Source |
|---|---|---|---|---|
| CRBN (D8H3S) Rabbit mAb | 71810 | 20 µl | 55 kDa | Rabbit IgG |
| VHL Antibody | 68547 | 20 µl | 18-22 kDa | Rabbit |
| c-IAP1 (D5G9) Rabbit mAb | 7065 | 20 µl | 62 kDa | Rabbit IgG |
| KEAP1 (D6B12) Rabbit mAb | 8047 | 20 µl | 60-64 kDa | Rabbit IgG |
| MDM2 (D1V2Z) Rabbit mAb | 86934 | 20 µl | 90 kDa | Rabbit IgG |
| β-TrCP (D13F10) Rabbit mAb | 4394 | 20 µl | 62 kDa | Rabbit IgG |
| XIAP (D2Z8W) Rabbit mAb | 14334 | 20 µl | 53 kDa | Rabbit IgG |
| Anti-rabbit IgG, HRP-linked Antibody | 7074 | 100 µl | Goat |
Please visit cellsignal.com for individual component applications, species cross-reactivity, dilutions, protocols, and additional product information.
Description
The PROTAC E3 Ligase Profiling Antibody Sampler Kit provides an economical means of detecting selected PROTAC E3 ligases. The kit includes enough antibodies to perform two western blot experiments with each primary antibody.
Storage
Background
PROTAC (proteolysis-targeting chimera) is a technique that uses a class of small molecules to target specific proteins for degradation (1). The small molecules are heterobifunctional, consisting of two protein binding parts joined by a linker. One part of the molecule binds a protein of interest (POI), while the other part binds to an E3 ubiquitin ligase, bringing the E3 ligase close to the POI for ubiquitination coupled protein degradation (2). The first successful PROTAC study used the chimeric PROTAC-1 molecule to recruit the β-TrCP E3 ligase to dictate the ubiquitination and degradation of MetAP2 (3). There are over 600 E3 ligases, and only a few have been successfully developed by PROTAC to degrade target proteins (4). Among them, CRBN- and VHL-based PROTAC have been extensively explored and successfully applied for multiple disease treatments (5,6). The E3 ligased MDM2, c-IAP, and XIAP are fruitful in using PROTAC strategy for cancer treatment (7-9). PROTAC design using the KEAP1 E3 ligase has been developed for degradation of BRD3, BRD4, and Tau. KEAP1 is another promising member of the PROTAC team (10,11).
- Békés, M. et al. (2022) Nat Rev Drug Discov 21, 181-200.
- Li, X. and Song, Y. (2020) J Hematol Oncol 13, 50.
- Sakamoto, K.M. et al. (2001) Proc Natl Acad Sci USA 98, 8554-9.
- Zou, Y. et al. (2019) Cell Biochem Funct 37, 21-30.
- Wang, C. et al. (2021) Eur J Med Chem 225, 113749.
- Wang, C. et al. (2022) Eur J Med Chem 227, 113906.
- Naito, M. et al. (2019) Drug Discov Today Technol 31, 35-42.
- Vicente, A.T.S. and Salvador, J.A.R. (2022) Int J Mol Sci 23, 11068. doi: 10.3390/ijms231911068.
- Park, S. et al. (2023) Eur J Med Chem 245, 114910.
- Wei, J. et al. (2021) J Am Chem Soc 143, 15073-15083.
- Lu, M. et al. (2018) Eur J Med Chem 146, 251-259.
Background References
Trademarks and Patents
Limited Uses
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