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ac devd afc  (MedChemExpress)


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    Structured Review

    MedChemExpress ac devd afc
    Action of cetuximab-vc-MMAF on cell viability. A. Flow cytometry-based apoptosis assay of cells treated with the cetuximab-vc-MMAF (10 nM) for the indicated times. Live cells are shown in the lower left quadrant (Annexin V-/PI-), while the other three quadrants represent different stages of non-viable cells. B. Graphical representation of non-viable cells for each condition. Data are plotted as mean ± SD of three independent experiments. C. Western blot analysis of apoptosis-related proteins at the indicated time points following treatment with 10 nM cetuximab-vc-MMAF. Actin was used as a loading control, and molecular weight markers are shown at the right. D. Analysis of caspase-3 activity in cells treated with cetuximab-vc-MMAF (10 nM) for the indicated times. Data represent mean ± SD of fluorescence intensity resulting from substrate cleavage <t>(Ac-DEVD-AFC)</t> by activated caspase-3 in two independent experiments.
    Ac Devd Afc, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 16 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ac+devd+afc/Ac-DEVD-AFC/pmc12997193-46-32-44
    Average 94 stars, based on 16 article reviews
    ac devd afc - by Bioz Stars, 2026-10
    94/100 stars

    Images

    1) Product Images from "Rational payload selection enables high antitumoral efficacy of an anti-EGFR antibody-drug conjugate against ovarian tumors"

    Article Title: Rational payload selection enables high antitumoral efficacy of an anti-EGFR antibody-drug conjugate against ovarian tumors

    Journal: Neoplasia (New York, N.Y.)

    doi: 10.1016/j.neo.2026.101295

    Action of cetuximab-vc-MMAF on cell viability. A. Flow cytometry-based apoptosis assay of cells treated with the cetuximab-vc-MMAF (10 nM) for the indicated times. Live cells are shown in the lower left quadrant (Annexin V-/PI-), while the other three quadrants represent different stages of non-viable cells. B. Graphical representation of non-viable cells for each condition. Data are plotted as mean ± SD of three independent experiments. C. Western blot analysis of apoptosis-related proteins at the indicated time points following treatment with 10 nM cetuximab-vc-MMAF. Actin was used as a loading control, and molecular weight markers are shown at the right. D. Analysis of caspase-3 activity in cells treated with cetuximab-vc-MMAF (10 nM) for the indicated times. Data represent mean ± SD of fluorescence intensity resulting from substrate cleavage (Ac-DEVD-AFC) by activated caspase-3 in two independent experiments.
    Figure Legend Snippet: Action of cetuximab-vc-MMAF on cell viability. A. Flow cytometry-based apoptosis assay of cells treated with the cetuximab-vc-MMAF (10 nM) for the indicated times. Live cells are shown in the lower left quadrant (Annexin V-/PI-), while the other three quadrants represent different stages of non-viable cells. B. Graphical representation of non-viable cells for each condition. Data are plotted as mean ± SD of three independent experiments. C. Western blot analysis of apoptosis-related proteins at the indicated time points following treatment with 10 nM cetuximab-vc-MMAF. Actin was used as a loading control, and molecular weight markers are shown at the right. D. Analysis of caspase-3 activity in cells treated with cetuximab-vc-MMAF (10 nM) for the indicated times. Data represent mean ± SD of fluorescence intensity resulting from substrate cleavage (Ac-DEVD-AFC) by activated caspase-3 in two independent experiments.

    Techniques Used: Flow Cytometry, Apoptosis Assay, Western Blot, Control, Molecular Weight, Activity Assay, Fluorescence

    Related Articles

    Concentration Assay:

    Article Title: Spotted seabass Lateolabrax maculatus GSDMEa: a pyroptosis executor activated by CASP3/7 during bacterial infection.
    Article Snippet: Pyroptosis is a lytic form of programmed cell death executed by gasdermin, which is activated by caspase (CASP) cleavage.. Pyroptosis plays a pivotal role in host defense against bacterial infection.. Spotted seabass Lateolabrax maculatus, one of the major aquaculture fish in China, is vulnerable to the bacterial pathogen Photobacterium damselae subsp. piscicida (PDP), which causes significant economic losses due to high mortality outbreaks.

    Article Title: Compositions and methods for inhibiting M
    Article Snippet: .. Calpain I, Cathepsin L and Cathepsin K enzymatic assays were carried as previously described.33 Caspase-3 enzymatic assay was carried out as follows: 1 unit Caspase-3 protein was diluted into 1600 μl reaction buffer (20 mM HEPES pH7.4, 2 mM EDTA, 0.1% CHAPS and 5 mM DTT); 100 μl diluted protein was incubated with 1 μl various concentration of testing compounds for 30 min at 30° C.; the enzymatic reaction was initiated by adding 1 μl of 2 mM Ac-DEVD-AFC (Medchemexpress, Catalog #HY-P1005). .. The reaction was monitored a Molecular Devices SpectraMax iD3 plate reader with excitation at 400 nm and emission at 505 nm at 30° C. for 1 hour.

    Incubation:

    Article Title: Spotted seabass Lateolabrax maculatus GSDMEa: a pyroptosis executor activated by CASP3/7 during bacterial infection.
    Article Snippet: Pyroptosis is a lytic form of programmed cell death executed by gasdermin, which is activated by caspase (CASP) cleavage.. Pyroptosis plays a pivotal role in host defense against bacterial infection.. Spotted seabass Lateolabrax maculatus, one of the major aquaculture fish in China, is vulnerable to the bacterial pathogen Photobacterium damselae subsp. piscicida (PDP), which causes significant economic losses due to high mortality outbreaks.

    Article Title: Compositions and methods for inhibiting M
    Article Snippet: .. Calpain I, Cathepsin L and Cathepsin K enzymatic assays were carried as previously described.33 Caspase-3 enzymatic assay was carried out as follows: 1 unit Caspase-3 protein was diluted into 1600 μl reaction buffer (20 mM HEPES pH7.4, 2 mM EDTA, 0.1% CHAPS and 5 mM DTT); 100 μl diluted protein was incubated with 1 μl various concentration of testing compounds for 30 min at 30° C.; the enzymatic reaction was initiated by adding 1 μl of 2 mM Ac-DEVD-AFC (Medchemexpress, Catalog #HY-P1005). .. The reaction was monitored a Molecular Devices SpectraMax iD3 plate reader with excitation at 400 nm and emission at 505 nm at 30° C. for 1 hour.

    Article Title: Characterization of the Apoptotic and Antimicrobial Activities of Two Initiator Caspases of Sea Cucumber Apostichopus japonicus
    Article Snippet: .. Briefly, the lysates were incubated with commercial fluorogenic substrates Ac-YVAD-AFC, Ac-VDVAD-AFC, Ac-DEVD-AFC, Ac-VEID-AFC, Ac-IETD-AFC, and Ac-LEHD-AFC (MedChem Express, Princeton, NJ, USA) in a 100 μL reaction system containing 50 mM HEPES (pH 7.5), 3 mM EDTA, 150 mM NaCl, 0.005% ( v / v ) Tween 20, and 10 mM DTT. .. Briefly, the lysates were incubated with commercial fluorogenic substrates Ac-YVAD-AFC, Ac-VDVAD-AFC, Ac-DEVD-AFC, Ac-VEID-AFC, Ac-IETD-AFC, and Ac-LEHD-AFC (MedChem Express, Princeton, NJ, USA) in a 100 μL reaction system containing 50 mM HEPES (pH 7.5), 3 mM EDTA, 150 mM NaCl, 0.005% ( v / v ) Tween 20, and 10 mM DTT.

    Enzymatic Assay:

    Article Title: Compositions and methods for inhibiting M
    Article Snippet: .. Calpain I, Cathepsin L and Cathepsin K enzymatic assays were carried as previously described.33 Caspase-3 enzymatic assay was carried out as follows: 1 unit Caspase-3 protein was diluted into 1600 μl reaction buffer (20 mM HEPES pH7.4, 2 mM EDTA, 0.1% CHAPS and 5 mM DTT); 100 μl diluted protein was incubated with 1 μl various concentration of testing compounds for 30 min at 30° C.; the enzymatic reaction was initiated by adding 1 μl of 2 mM Ac-DEVD-AFC (Medchemexpress, Catalog #HY-P1005). .. The reaction was monitored a Molecular Devices SpectraMax iD3 plate reader with excitation at 400 nm and emission at 505 nm at 30° C. for 1 hour.

    Conjugation Assay:

    Article Title: Rational payload selection enables high antitumoral efficacy of an anti-EGFR antibody-drug conjugate against ovarian tumors
    Article Snippet: The Immobilon®-P transfer membranes, Bovine Serum Albumin (BSA), Hoechst 33342, and Matrigel were obtained from Merck Millipore Corp. (Darmstadt, Germany). .. The payloads used for antibodies conjugation, MC-GGFG-DXD (DXd, catalog reference: HY-13631E), MC-Val-Cit-PAB-MMAF (Vc-MMAF, catalog reference: HY-112786) and McMMAF (catalog reference: HY-15578), the belantamab mafodotin ADC (catalog reference: HY-P3239), as well as the Ac-DEVD-AFC (catalog reference: HY-P1005) substrate for caspase-3 activity detection, were purchased from MedChem Express (Princeton, NJ, USA). .. The SMCC-DM1 cytotoxin (catalog reference: SET0101) was obtained from Levena (Tokyo, Japan).

    Article Title: Rational payload selection enables high antitumoral efficacy of an anti-EGFR antibody-drug conjugate against ovarian tumors.
    Article Snippet: The Immobilon®-P transfer membranes, Bovine Serum Albumin (BSA), Hoechst 33342, and Matrigel were obtained from Merck Millipore Corp. (Darmstadt, Germany). .. The payloads used for antibodies conjugation, MC-GGFG-DXD (DXd, catalog reference: HY-13631E), MCVal-Cit-PAB-MMAF (Vc-MMAF, catalog reference: HY-112786) and McMMAF (catalog reference: HY-15578), the belantamab mafodotin ADC (catalog reference: HY-P3239), as well as the Ac-DEVD-AFC (catalog reference: HY-P1005) substrate for caspase-3 activity detection, were purchased from MedChem Express (Princeton, NJ, USA). .. The SMCC-DM1 cytotoxin (catalog reference: SET0101) was obtained from Levena (Tokyo, Japan).

    Activity Assay:

    Article Title: Rational payload selection enables high antitumoral efficacy of an anti-EGFR antibody-drug conjugate against ovarian tumors
    Article Snippet: The Immobilon®-P transfer membranes, Bovine Serum Albumin (BSA), Hoechst 33342, and Matrigel were obtained from Merck Millipore Corp. (Darmstadt, Germany). .. The payloads used for antibodies conjugation, MC-GGFG-DXD (DXd, catalog reference: HY-13631E), MC-Val-Cit-PAB-MMAF (Vc-MMAF, catalog reference: HY-112786) and McMMAF (catalog reference: HY-15578), the belantamab mafodotin ADC (catalog reference: HY-P3239), as well as the Ac-DEVD-AFC (catalog reference: HY-P1005) substrate for caspase-3 activity detection, were purchased from MedChem Express (Princeton, NJ, USA). .. The SMCC-DM1 cytotoxin (catalog reference: SET0101) was obtained from Levena (Tokyo, Japan).

    Article Title: Paralichthys olivaceus GSDME-mediated pyroptosis is regulated by multiple caspases in different manners.
    Article Snippet: Pyroptosis is a type of programmed cell death mediated by gasdermin (GSDM).. GSDM is activated by caspase (CASP), which cleaves GSDM to release the N-terminal (NT) fragment that forms channels in the plasma membrane and leads to cell death.. To date, research on pyroptosis in teleost is limited.

    Article Title: Rational payload selection enables high antitumoral efficacy of an anti-EGFR antibody-drug conjugate against ovarian tumors.
    Article Snippet: The Immobilon®-P transfer membranes, Bovine Serum Albumin (BSA), Hoechst 33342, and Matrigel were obtained from Merck Millipore Corp. (Darmstadt, Germany). .. The payloads used for antibodies conjugation, MC-GGFG-DXD (DXd, catalog reference: HY-13631E), MCVal-Cit-PAB-MMAF (Vc-MMAF, catalog reference: HY-112786) and McMMAF (catalog reference: HY-15578), the belantamab mafodotin ADC (catalog reference: HY-P3239), as well as the Ac-DEVD-AFC (catalog reference: HY-P1005) substrate for caspase-3 activity detection, were purchased from MedChem Express (Princeton, NJ, USA). .. The SMCC-DM1 cytotoxin (catalog reference: SET0101) was obtained from Levena (Tokyo, Japan).

    Lysis:

    Article Title: Paralichthys olivaceus GSDME-mediated pyroptosis is regulated by multiple caspases in different manners.
    Article Snippet: Pyroptosis is a type of programmed cell death mediated by gasdermin (GSDM).. GSDM is activated by caspase (CASP), which cleaves GSDM to release the N-terminal (NT) fragment that forms channels in the plasma membrane and leads to cell death.. To date, research on pyroptosis in teleost is limited.

    CCK-8 Assay:

    Article Title: Signaling Mechanism of Cuproptosis Activating cGAS-STING Immune Pathway
    Article Snippet: .. Ac-DEVD-AFC, GM-CSF, Cell Counting Kit-8, and IL-4 were purchased from Medchemexpress Co., ltd.; Hoechst 33342 (C1026) was purchased from Beyotime Biotechnology. .. Reagent Pro (MI20201); MR05101MonScript RTIII All-in-One Mix with dsDNase (MR05101) and MonAmp SYBR Green qPCR Mix (Low ROX) (MQ10201) were purchased from Mona Biotechnology Co., Ltd.; IFN-β(EMC016.96), TNF-α(EMC102a(H).96), IFNγ(EMC101g(H).96) ELISA kit was purchased from Neobioscience.



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    Action of cetuximab-vc-MMAF on cell viability. A. Flow cytometry-based apoptosis assay of cells treated with the cetuximab-vc-MMAF (10 nM) for the indicated times. Live cells are shown in the lower left quadrant (Annexin V-/PI-), while the other three quadrants represent different stages of non-viable cells. B. Graphical representation of non-viable cells for each condition. Data are plotted as mean ± SD of three independent experiments. C. Western blot analysis of apoptosis-related proteins at the indicated time points following treatment with 10 nM cetuximab-vc-MMAF. Actin was used as a loading control, and molecular weight markers are shown at the right. D. Analysis of caspase-3 activity in cells treated with cetuximab-vc-MMAF (10 nM) for the indicated times. Data represent mean ± SD of fluorescence intensity resulting from substrate cleavage <t>(Ac-DEVD-AFC)</t> by activated caspase-3 in two independent experiments.
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    Action of cetuximab-vc-MMAF on cell viability. A. Flow cytometry-based apoptosis assay of cells treated with the cetuximab-vc-MMAF (10 nM) for the indicated times. Live cells are shown in the lower left quadrant (Annexin V-/PI-), while the other three quadrants represent different stages of non-viable cells. B. Graphical representation of non-viable cells for each condition. Data are plotted as mean ± SD of three independent experiments. C. Western blot analysis of apoptosis-related proteins at the indicated time points following treatment with 10 nM cetuximab-vc-MMAF. Actin was used as a loading control, and molecular weight markers are shown at the right. D. Analysis of caspase-3 activity in cells treated with cetuximab-vc-MMAF (10 nM) for the indicated times. Data represent mean ± SD of fluorescence intensity resulting from substrate cleavage <t>(Ac-DEVD-AFC)</t> by activated caspase-3 in two independent experiments.
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    Image Search Results


    Action of cetuximab-vc-MMAF on cell viability. A. Flow cytometry-based apoptosis assay of cells treated with the cetuximab-vc-MMAF (10 nM) for the indicated times. Live cells are shown in the lower left quadrant (Annexin V-/PI-), while the other three quadrants represent different stages of non-viable cells. B. Graphical representation of non-viable cells for each condition. Data are plotted as mean ± SD of three independent experiments. C. Western blot analysis of apoptosis-related proteins at the indicated time points following treatment with 10 nM cetuximab-vc-MMAF. Actin was used as a loading control, and molecular weight markers are shown at the right. D. Analysis of caspase-3 activity in cells treated with cetuximab-vc-MMAF (10 nM) for the indicated times. Data represent mean ± SD of fluorescence intensity resulting from substrate cleavage (Ac-DEVD-AFC) by activated caspase-3 in two independent experiments.

    Journal: Neoplasia (New York, N.Y.)

    Article Title: Rational payload selection enables high antitumoral efficacy of an anti-EGFR antibody-drug conjugate against ovarian tumors

    doi: 10.1016/j.neo.2026.101295

    Figure Lengend Snippet: Action of cetuximab-vc-MMAF on cell viability. A. Flow cytometry-based apoptosis assay of cells treated with the cetuximab-vc-MMAF (10 nM) for the indicated times. Live cells are shown in the lower left quadrant (Annexin V-/PI-), while the other three quadrants represent different stages of non-viable cells. B. Graphical representation of non-viable cells for each condition. Data are plotted as mean ± SD of three independent experiments. C. Western blot analysis of apoptosis-related proteins at the indicated time points following treatment with 10 nM cetuximab-vc-MMAF. Actin was used as a loading control, and molecular weight markers are shown at the right. D. Analysis of caspase-3 activity in cells treated with cetuximab-vc-MMAF (10 nM) for the indicated times. Data represent mean ± SD of fluorescence intensity resulting from substrate cleavage (Ac-DEVD-AFC) by activated caspase-3 in two independent experiments.

    Article Snippet: The payloads used for antibodies conjugation, MC-GGFG-DXD (DXd, catalog reference: HY-13631E), MC-Val-Cit-PAB-MMAF (Vc-MMAF, catalog reference: HY-112786) and McMMAF (catalog reference: HY-15578), the belantamab mafodotin ADC (catalog reference: HY-P3239), as well as the Ac-DEVD-AFC (catalog reference: HY-P1005) substrate for caspase-3 activity detection, were purchased from MedChem Express (Princeton, NJ, USA).

    Techniques: Flow Cytometry, Apoptosis Assay, Western Blot, Control, Molecular Weight, Activity Assay, Fluorescence