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Lactacystin (CAT#: ADC-P-106)
ADCs Toxins, Lactacystin is a cell-permeable, potent and selective proteasome inhibitor. A Streptomyces metabolite that is thought to bind irreversibly to the active site N-terminal threonine residue of the catalytic β-subunit of the 20S proteasome, thereby inhibiting its chymotrypsin and trypsin-like activities. Lactacystin induces neurite outgrowth in Neuro 2a neuroblastoma cells and has been reported to induce apoptosis in human monoblast U937 cells.
- Product Information
- CAS NO
- 133343-34-7
- Description
- ADCs Toxins, Lactacystin is a cell-permeable, potent and selective proteasome inhibitor. A Streptomyces metabolite that is thought to bind irreversibly to the active site N-terminal threonine residue of the catalytic β-subunit of the 20S proteasome, thereby inhibiting its chymotrypsin and trypsin-like activities. Lactacystin induces neurite outgrowth in Neuro 2a neuroblastoma cells and has been reported to induce apoptosis in human monoblast U937 cells.
- Classification
- Others
- Molecular Weight
- 376.43
- Purity
- 95%
For Research Use Only. NOT FOR CLINICAL USE.
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Customer Reviews
FAQ
Excellent
Lactacystin proved to be an essential tool in our neuroblastoma research. It effectively induced neurite outgrowth in Neuro 2a cells, offering valuable insights into neurodegenerative disease models.
Excellent
I used Lactacystin in ADC research, and it performed well as a proteasome inhibitor. Its ability to block proteasomal activity enhanced the cytotoxic effects of our ADCs on targeted cells.
Excellent
Lactacystin significantly inhibited the proteasome's chymotrypsin and trypsin-like activities in my assays, leading to reliable induction of apoptosis in U937 cells. A great addition to our lab's tools.
Excellent
In ADC development, Lactacystin has proven highly effective. Its proteasome inhibition mechanism synergized well with the payloads in our targeted therapy experiments, providing strong therapeutic effects.
Excellent
I applied Lactacystin to human U937 monoblast cells, and it consistently induced apoptosis. This product is highly effective for research focused on programmed cell death mechanisms.
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