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Caspase 3 ac devd amc

Manufactured by Enzo Life Sciences
Sourced in Switzerland, United States

Caspase 3 (AC-DEVD-AMC) is a fluorogenic substrate used for the detection and measurement of caspase-3 activity. Caspase-3 is a key executioner caspase involved in the apoptosis (programmed cell death) pathway. The AC-DEVD-AMC substrate contains the caspase-3 cleavage sequence DEVD, which, upon cleavage by active caspase-3, releases the fluorescent AMC (7-amino-4-methylcoumarin) moiety, allowing for quantitative measurement of caspase-3 activity.

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2 protocols using caspase 3 ac devd amc

1

Apoptosis and Mitochondrial Assays

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Caspase 3 (AC-DEVD-AMC) and Caspase 9 (AC-LEHD-AMC) substrates were obtained from Enzo (Lausen, Switzerland). APOPercentage assays with releasing buffer were obtained from Biocolor (Belfast, Northern Ireland). A mitochondrial stain 5,50, 6,60-tetrachloro-1,10,3,30-tetraethylbenzimidazolyl carbocyanine iodide (JC-1) and Probenecid were obtained from Santa Cruz (Dallas, Texas, USA). Pluronic® F-127 was obtained from Biovision(San Francisco, USA). Dihydrorhodamine-123 (DHR 123), was obtained from Sigma Aldrich (St. Louis, MO), Fura-2 AM calcium fl orescent dye was obtained from Calbiochem (Darmstadt, Germany).
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2

Isoquercitrin Extraction and Characterization

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Organic solvents of analytical grade were purchased either from POCh S.A. (Gliwice, Poland) or from Merck (Darmstadt, Germany). Water was purified by a Milli-Q system (Millipore Corp., Bedford, MA, USA). MeOH and MeCN of HPLC grade were purchased from Merck (Darmstadt, Germany). Dulbecco’s Modified Eagle’s Medium (DMEM) and fetal bovine serum (FBS) were from Gibco (Invitrogen, Paisley, UK). WST-1 assay was purchased from Roche Diagnostic (Basel, Switzerland). Caspase-3 (Ac-DEVD-AMC) and cathepsin D (MOCA-Gly-Lys-Pro-Ile-Leu-Phe-Phe-Arg-Leu-Lys(Dnp)-D-Arg-NH2) fluorogenic substrates were obtained from Enzo Life Sciences (New York, NY, USA). All other reagents were from Sigma (Sigma-Aldrich Chemie GmbH, Schnelldorf, Germany). Isoquercitrin (purity > 95% by HPLC) was isolated from flowers of Xerolekia speciosissima (L.) Anderb. [60 (link)].
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