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fluorogenic substrate suc leu leu val tyr amc  (MedChemExpress)


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    Structured Review

    MedChemExpress fluorogenic substrate suc leu leu val tyr amc
    Fluorogenic Substrate Suc Leu Leu Val Tyr Amc, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 19 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fluorogenic+substrate+suc+leu+leu+val+tyr+amc/Suc-Leu-Leu-Val-Tyr-AMC/pm41475191-46-6-12
    Average 94 stars, based on 19 article reviews
    fluorogenic substrate suc leu leu val tyr amc - by Bioz Stars, 2026-09
    94/100 stars

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    other:

    Article Title: PRRSV Nsp12 targets PSMA2 to suppress host proteasome activity and promote viral survival.
    Article Snippet: Porcine reproductive and respiratory syndrome virus (PRRSV) poses a significant threat to the global swine industry, employing complex mechanisms to interact with the host and evade host immune responses.. The ubiquitin-proteasome system (UPS) is central to host antiviral innate immunity, yet its interplay with PRRSV remains poorly understood.. In this study, Proteasome 20S Subunit Alpha 2 (PSMA2) was identified as a novel host restriction factor against highly pathogenic PRRSV (HP-PRRSV).



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    Boston Biochem fluorogenic proteasome substrate suc llvy amc
    Fig. 4. Evaluation of the effects of pesticides using the <t>proteasome</t> activities as endpoints. Cells were exposed to each pesticide (100 µM) or MG-132 (1 µM) as a positive control for 24 h, and then (A) chymotrypsin-like (Suc-LLVY-AMC) and (B) caspase-like (Z-LLE-AMC) proteasome activities were monitored by AMC- conjugated fluorescence substrates. All data are shown as the mean ± SD. * p < 0.05, * * p < 0.01 vs. the control group (one-way ANOVA followed by Dunnett’s post-hoc test).
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    Fig. 4. Evaluation of the effects of pesticides using the proteasome activities as endpoints. Cells were exposed to each pesticide (100 µM) or MG-132 (1 µM) as a positive control for 24 h, and then (A) chymotrypsin-like (Suc-LLVY-AMC) and (B) caspase-like (Z-LLE-AMC) proteasome activities were monitored by AMC- conjugated fluorescence substrates. All data are shown as the mean ± SD. * p < 0.05, * * p < 0.01 vs. the control group (one-way ANOVA followed by Dunnett’s post-hoc test).

    Journal: Toxicology

    Article Title: An adverse outcome pathway-based approach to assess the neurotoxicity by combined exposure to current-use pesticides.

    doi: 10.1016/j.tox.2023.153687

    Figure Lengend Snippet: Fig. 4. Evaluation of the effects of pesticides using the proteasome activities as endpoints. Cells were exposed to each pesticide (100 µM) or MG-132 (1 µM) as a positive control for 24 h, and then (A) chymotrypsin-like (Suc-LLVY-AMC) and (B) caspase-like (Z-LLE-AMC) proteasome activities were monitored by AMC- conjugated fluorescence substrates. All data are shown as the mean ± SD. * p < 0.05, * * p < 0.01 vs. the control group (one-way ANOVA followed by Dunnett’s post-hoc test).

    Article Snippet: The proteasome assay buffer (100 μL) [50 mM HEPES buffer (pH 7.8) containing 10 mM NaCl, 1.5 mM MgCl2, 1 mM EDTA, 1 mM EGTA, 250 mM sucrose, 5 mM DTT and 2 mM ATP] containing 2.5 μM of the fluorogenic proteasome substrate Suc-LLVY-AMC (succinyl-Leu-Leu-Val-Tyr-7-amino-4-methylcoumarin, #S-280) and Z-LLE-AMC (Z-Leu-Leu-Glu-7-amino-4methylcoumarin, #S-230; Boston Biochem, Cambridge, MA, USA) were added to the lysate sample (25 μL) in a 96-well black plate and incubated at 37 ◦C for 30 min.

    Techniques: Pesticides, Positive Control, Fluorescence, Control