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colorimetric ace kit wst  (Dojindo Labs)


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    Dojindo Labs colorimetric ace kit wst
    Anti‐hypertensive and anti‐adipogenic effects of aqueous and ethanolic larval extracts. (a) Angiotensin‐converting enzyme <t>(ACE)</t> inhibitory activity of larval extracts at the indicated concentrations (20–300 μg/mL), measured using a <t>colorimetric</t> <t>ACE</t> <t>Kit‐WST</t> assay according to the manufacturer's instructions. Results are expressed as percentage inhibition relative to untreated control. (b) Effects of larval extracts on intracellular lipid accumulation in differentiated 3T3‐L1 adipocytes. Cells were induced to differentiate for 8 days in the presence or absence of extracts (100–400 μg/mL), and lipid accumulation was quantified by Oil Red O staining at 520 nm. Untreated differentiated cells (−) served as control group. Data are expressed as mean ± SD from three independent biological experiments ( n = 3), each performed in triplicate. * p < 0.05 versus control.
    Colorimetric Ace Kit Wst, supplied by Dojindo Labs, used in various techniques. Bioz Stars score: 95/100, based on 180 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ace+kit+wst+kit/pmc13136604-69-6-9?v=Dojindo+Labs
    Average 95 stars, based on 180 article reviews
    colorimetric ace kit wst - by Bioz Stars, 2026-07
    95/100 stars

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    1) Product Images from "Solvent‐Dependent Biological Activities of Aqueous and Ethanolic Extracts From Edible Insect Larvae"

    Article Title: Solvent‐Dependent Biological Activities of Aqueous and Ethanolic Extracts From Edible Insect Larvae

    Journal: Food Science & Nutrition

    doi: 10.1002/fsn3.71848

    Anti‐hypertensive and anti‐adipogenic effects of aqueous and ethanolic larval extracts. (a) Angiotensin‐converting enzyme (ACE) inhibitory activity of larval extracts at the indicated concentrations (20–300 μg/mL), measured using a colorimetric ACE Kit‐WST assay according to the manufacturer's instructions. Results are expressed as percentage inhibition relative to untreated control. (b) Effects of larval extracts on intracellular lipid accumulation in differentiated 3T3‐L1 adipocytes. Cells were induced to differentiate for 8 days in the presence or absence of extracts (100–400 μg/mL), and lipid accumulation was quantified by Oil Red O staining at 520 nm. Untreated differentiated cells (−) served as control group. Data are expressed as mean ± SD from three independent biological experiments ( n = 3), each performed in triplicate. * p < 0.05 versus control.
    Figure Legend Snippet: Anti‐hypertensive and anti‐adipogenic effects of aqueous and ethanolic larval extracts. (a) Angiotensin‐converting enzyme (ACE) inhibitory activity of larval extracts at the indicated concentrations (20–300 μg/mL), measured using a colorimetric ACE Kit‐WST assay according to the manufacturer's instructions. Results are expressed as percentage inhibition relative to untreated control. (b) Effects of larval extracts on intracellular lipid accumulation in differentiated 3T3‐L1 adipocytes. Cells were induced to differentiate for 8 days in the presence or absence of extracts (100–400 μg/mL), and lipid accumulation was quantified by Oil Red O staining at 520 nm. Untreated differentiated cells (−) served as control group. Data are expressed as mean ± SD from three independent biological experiments ( n = 3), each performed in triplicate. * p < 0.05 versus control.

    Techniques Used: Activity Assay, WST Assay, Inhibition, Control, Staining



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    Anti‐hypertensive and anti‐adipogenic effects of aqueous and ethanolic larval extracts. (a) Angiotensin‐converting enzyme <t>(ACE)</t> inhibitory activity of larval extracts at the indicated concentrations (20–300 μg/mL), measured using a <t>colorimetric</t> <t>ACE</t> <t>Kit‐WST</t> assay according to the manufacturer's instructions. Results are expressed as percentage inhibition relative to untreated control. (b) Effects of larval extracts on intracellular lipid accumulation in differentiated 3T3‐L1 adipocytes. Cells were induced to differentiate for 8 days in the presence or absence of extracts (100–400 μg/mL), and lipid accumulation was quantified by Oil Red O staining at 520 nm. Untreated differentiated cells (−) served as control group. Data are expressed as mean ± SD from three independent biological experiments ( n = 3), each performed in triplicate. * p < 0.05 versus control.
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    Anti‐hypertensive and anti‐adipogenic effects of aqueous and ethanolic larval extracts. (a) Angiotensin‐converting enzyme (ACE) inhibitory activity of larval extracts at the indicated concentrations (20–300 μg/mL), measured using a colorimetric ACE Kit‐WST assay according to the manufacturer's instructions. Results are expressed as percentage inhibition relative to untreated control. (b) Effects of larval extracts on intracellular lipid accumulation in differentiated 3T3‐L1 adipocytes. Cells were induced to differentiate for 8 days in the presence or absence of extracts (100–400 μg/mL), and lipid accumulation was quantified by Oil Red O staining at 520 nm. Untreated differentiated cells (−) served as control group. Data are expressed as mean ± SD from three independent biological experiments ( n = 3), each performed in triplicate. * p < 0.05 versus control.

    Journal: Food Science & Nutrition

    Article Title: Solvent‐Dependent Biological Activities of Aqueous and Ethanolic Extracts From Edible Insect Larvae

    doi: 10.1002/fsn3.71848

    Figure Lengend Snippet: Anti‐hypertensive and anti‐adipogenic effects of aqueous and ethanolic larval extracts. (a) Angiotensin‐converting enzyme (ACE) inhibitory activity of larval extracts at the indicated concentrations (20–300 μg/mL), measured using a colorimetric ACE Kit‐WST assay according to the manufacturer's instructions. Results are expressed as percentage inhibition relative to untreated control. (b) Effects of larval extracts on intracellular lipid accumulation in differentiated 3T3‐L1 adipocytes. Cells were induced to differentiate for 8 days in the presence or absence of extracts (100–400 μg/mL), and lipid accumulation was quantified by Oil Red O staining at 520 nm. Untreated differentiated cells (−) served as control group. Data are expressed as mean ± SD from three independent biological experiments ( n = 3), each performed in triplicate. * p < 0.05 versus control.

    Article Snippet: ACE‐inhibitory activity was measured using a colorimetric ACE Kit‐WST (Dojindo, Japan) following the manufacturer's protocol (Kim et al. ).

    Techniques: Activity Assay, WST Assay, Inhibition, Control, Staining