saturated aqueous uranyl acetate solution and sato lead stain Search Results


93
Addgene inc sat1 cds
( A ) Diagram of the hypothesis of PBA-derived phenylacetyl-CoA competing with acetyl-CoA to interfere with <t>SAT1-mediated</t> polyamine catabolism and acetyl-CoA consumption. SPDSY, spermidine synthase; PAO: peroxisomal N 1 -acetyl-spermine/spermidine oxidase; SMOX, spermine oxidase. ( B ) Acetyl-CoA level in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. Cells from 4 separate experiments were stored at –80°C and then tested in a single plate. n = 4; 1-way ANOVA multiple comparisons (matched). ( C ) Dot blot of acetyl-lysine in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. The values of the quantification were normalized with the control samples. ( D ) Western blot of the samples in C . Acetylated histones and nonhistone proteins in the bracket areas were quantified separately and normalized with β-Actin level. All values were further normalized by the control samples. ( E ) Western blot of HA-tagged SAT1 overexpressed in HEK293T cells with PBA, MG132, or the combination treatment. The HA-SAT1 level was normalized with the β-Actin level. The values of the cells without HA-SAT1 plasmid transfection were set as background. All the values were further normalized by that of the cells with indicated treatment. ( F ) Western blot of SAT1 induced by DENSPM in patient fibroblasts (CMS1849a) with indicated treatment. The SAT1 level was normalized with the β-Actin level. Values of the cells without DENSPM treatment were set as background. All values were further normalized by that of cells with DENSPM and without PBA or MG132 treatment. Images in C – F are representative of 3 separate experiments. n =3; * P < 0.05, ** P < 0.01, *** P < 0.001; 1-way ANOVA multiple comparisons (matched). Data represent mean ± SEM.
Sat1 Cds, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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( A ) Diagram of the hypothesis of PBA-derived phenylacetyl-CoA competing with acetyl-CoA to interfere with <t>SAT1-mediated</t> polyamine catabolism and acetyl-CoA consumption. SPDSY, spermidine synthase; PAO: peroxisomal N 1 -acetyl-spermine/spermidine oxidase; SMOX, spermine oxidase. ( B ) Acetyl-CoA level in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. Cells from 4 separate experiments were stored at –80°C and then tested in a single plate. n = 4; 1-way ANOVA multiple comparisons (matched). ( C ) Dot blot of acetyl-lysine in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. The values of the quantification were normalized with the control samples. ( D ) Western blot of the samples in C . Acetylated histones and nonhistone proteins in the bracket areas were quantified separately and normalized with β-Actin level. All values were further normalized by the control samples. ( E ) Western blot of HA-tagged SAT1 overexpressed in HEK293T cells with PBA, MG132, or the combination treatment. The HA-SAT1 level was normalized with the β-Actin level. The values of the cells without HA-SAT1 plasmid transfection were set as background. All the values were further normalized by that of the cells with indicated treatment. ( F ) Western blot of SAT1 induced by DENSPM in patient fibroblasts (CMS1849a) with indicated treatment. The SAT1 level was normalized with the β-Actin level. Values of the cells without DENSPM treatment were set as background. All values were further normalized by that of cells with DENSPM and without PBA or MG132 treatment. Images in C – F are representative of 3 separate experiments. n =3; * P < 0.05, ** P < 0.01, *** P < 0.001; 1-way ANOVA multiple comparisons (matched). Data represent mean ± SEM.
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90
Verlag GmbH data book on mechanical properties of living cells, tissues, and organs
( A ) Diagram of the hypothesis of PBA-derived phenylacetyl-CoA competing with acetyl-CoA to interfere with <t>SAT1-mediated</t> polyamine catabolism and acetyl-CoA consumption. SPDSY, spermidine synthase; PAO: peroxisomal N 1 -acetyl-spermine/spermidine oxidase; SMOX, spermine oxidase. ( B ) Acetyl-CoA level in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. Cells from 4 separate experiments were stored at –80°C and then tested in a single plate. n = 4; 1-way ANOVA multiple comparisons (matched). ( C ) Dot blot of acetyl-lysine in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. The values of the quantification were normalized with the control samples. ( D ) Western blot of the samples in C . Acetylated histones and nonhistone proteins in the bracket areas were quantified separately and normalized with β-Actin level. All values were further normalized by the control samples. ( E ) Western blot of HA-tagged SAT1 overexpressed in HEK293T cells with PBA, MG132, or the combination treatment. The HA-SAT1 level was normalized with the β-Actin level. The values of the cells without HA-SAT1 plasmid transfection were set as background. All the values were further normalized by that of the cells with indicated treatment. ( F ) Western blot of SAT1 induced by DENSPM in patient fibroblasts (CMS1849a) with indicated treatment. The SAT1 level was normalized with the β-Actin level. Values of the cells without DENSPM treatment were set as background. All values were further normalized by that of cells with DENSPM and without PBA or MG132 treatment. Images in C – F are representative of 3 separate experiments. n =3; * P < 0.05, ** P < 0.01, *** P < 0.001; 1-way ANOVA multiple comparisons (matched). Data represent mean ± SEM.
Data Book On Mechanical Properties Of Living Cells, Tissues, And Organs, supplied by Verlag GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Federation of European Neuroscience Societies satc protein
( A ) Diagram of the hypothesis of PBA-derived phenylacetyl-CoA competing with acetyl-CoA to interfere with <t>SAT1-mediated</t> polyamine catabolism and acetyl-CoA consumption. SPDSY, spermidine synthase; PAO: peroxisomal N 1 -acetyl-spermine/spermidine oxidase; SMOX, spermine oxidase. ( B ) Acetyl-CoA level in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. Cells from 4 separate experiments were stored at –80°C and then tested in a single plate. n = 4; 1-way ANOVA multiple comparisons (matched). ( C ) Dot blot of acetyl-lysine in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. The values of the quantification were normalized with the control samples. ( D ) Western blot of the samples in C . Acetylated histones and nonhistone proteins in the bracket areas were quantified separately and normalized with β-Actin level. All values were further normalized by the control samples. ( E ) Western blot of HA-tagged SAT1 overexpressed in HEK293T cells with PBA, MG132, or the combination treatment. The HA-SAT1 level was normalized with the β-Actin level. The values of the cells without HA-SAT1 plasmid transfection were set as background. All the values were further normalized by that of the cells with indicated treatment. ( F ) Western blot of SAT1 induced by DENSPM in patient fibroblasts (CMS1849a) with indicated treatment. The SAT1 level was normalized with the β-Actin level. Values of the cells without DENSPM treatment were set as background. All values were further normalized by that of cells with DENSPM and without PBA or MG132 treatment. Images in C – F are representative of 3 separate experiments. n =3; * P < 0.05, ** P < 0.01, *** P < 0.001; 1-way ANOVA multiple comparisons (matched). Data represent mean ± SEM.
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Makoto USA Inc makoto imai
( A ) Diagram of the hypothesis of PBA-derived phenylacetyl-CoA competing with acetyl-CoA to interfere with <t>SAT1-mediated</t> polyamine catabolism and acetyl-CoA consumption. SPDSY, spermidine synthase; PAO: peroxisomal N 1 -acetyl-spermine/spermidine oxidase; SMOX, spermine oxidase. ( B ) Acetyl-CoA level in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. Cells from 4 separate experiments were stored at –80°C and then tested in a single plate. n = 4; 1-way ANOVA multiple comparisons (matched). ( C ) Dot blot of acetyl-lysine in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. The values of the quantification were normalized with the control samples. ( D ) Western blot of the samples in C . Acetylated histones and nonhistone proteins in the bracket areas were quantified separately and normalized with β-Actin level. All values were further normalized by the control samples. ( E ) Western blot of HA-tagged SAT1 overexpressed in HEK293T cells with PBA, MG132, or the combination treatment. The HA-SAT1 level was normalized with the β-Actin level. The values of the cells without HA-SAT1 plasmid transfection were set as background. All the values were further normalized by that of the cells with indicated treatment. ( F ) Western blot of SAT1 induced by DENSPM in patient fibroblasts (CMS1849a) with indicated treatment. The SAT1 level was normalized with the β-Actin level. Values of the cells without DENSPM treatment were set as background. All values were further normalized by that of cells with DENSPM and without PBA or MG132 treatment. Images in C – F are representative of 3 separate experiments. n =3; * P < 0.05, ** P < 0.01, *** P < 0.001; 1-way ANOVA multiple comparisons (matched). Data represent mean ± SEM.
Makoto Imai, supplied by Makoto USA Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Verlag GmbH basics of corrosion chemistry, first edition
( A ) Diagram of the hypothesis of PBA-derived phenylacetyl-CoA competing with acetyl-CoA to interfere with <t>SAT1-mediated</t> polyamine catabolism and acetyl-CoA consumption. SPDSY, spermidine synthase; PAO: peroxisomal N 1 -acetyl-spermine/spermidine oxidase; SMOX, spermine oxidase. ( B ) Acetyl-CoA level in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. Cells from 4 separate experiments were stored at –80°C and then tested in a single plate. n = 4; 1-way ANOVA multiple comparisons (matched). ( C ) Dot blot of acetyl-lysine in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. The values of the quantification were normalized with the control samples. ( D ) Western blot of the samples in C . Acetylated histones and nonhistone proteins in the bracket areas were quantified separately and normalized with β-Actin level. All values were further normalized by the control samples. ( E ) Western blot of HA-tagged SAT1 overexpressed in HEK293T cells with PBA, MG132, or the combination treatment. The HA-SAT1 level was normalized with the β-Actin level. The values of the cells without HA-SAT1 plasmid transfection were set as background. All the values were further normalized by that of the cells with indicated treatment. ( F ) Western blot of SAT1 induced by DENSPM in patient fibroblasts (CMS1849a) with indicated treatment. The SAT1 level was normalized with the β-Actin level. Values of the cells without DENSPM treatment were set as background. All values were further normalized by that of cells with DENSPM and without PBA or MG132 treatment. Images in C – F are representative of 3 separate experiments. n =3; * P < 0.05, ** P < 0.01, *** P < 0.001; 1-way ANOVA multiple comparisons (matched). Data represent mean ± SEM.
Basics Of Corrosion Chemistry, First Edition, supplied by Verlag GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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TOSHO Co Inc liquid crystals
( A ) Diagram of the hypothesis of PBA-derived phenylacetyl-CoA competing with acetyl-CoA to interfere with <t>SAT1-mediated</t> polyamine catabolism and acetyl-CoA consumption. SPDSY, spermidine synthase; PAO: peroxisomal N 1 -acetyl-spermine/spermidine oxidase; SMOX, spermine oxidase. ( B ) Acetyl-CoA level in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. Cells from 4 separate experiments were stored at –80°C and then tested in a single plate. n = 4; 1-way ANOVA multiple comparisons (matched). ( C ) Dot blot of acetyl-lysine in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. The values of the quantification were normalized with the control samples. ( D ) Western blot of the samples in C . Acetylated histones and nonhistone proteins in the bracket areas were quantified separately and normalized with β-Actin level. All values were further normalized by the control samples. ( E ) Western blot of HA-tagged SAT1 overexpressed in HEK293T cells with PBA, MG132, or the combination treatment. The HA-SAT1 level was normalized with the β-Actin level. The values of the cells without HA-SAT1 plasmid transfection were set as background. All the values were further normalized by that of the cells with indicated treatment. ( F ) Western blot of SAT1 induced by DENSPM in patient fibroblasts (CMS1849a) with indicated treatment. The SAT1 level was normalized with the β-Actin level. Values of the cells without DENSPM treatment were set as background. All values were further normalized by that of cells with DENSPM and without PBA or MG132 treatment. Images in C – F are representative of 3 separate experiments. n =3; * P < 0.05, ** P < 0.01, *** P < 0.001; 1-way ANOVA multiple comparisons (matched). Data represent mean ± SEM.
Liquid Crystals, supplied by TOSHO Co Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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TANAKA SCIENTIFIC LIMITED funano, a
( A ) Diagram of the hypothesis of PBA-derived phenylacetyl-CoA competing with acetyl-CoA to interfere with <t>SAT1-mediated</t> polyamine catabolism and acetyl-CoA consumption. SPDSY, spermidine synthase; PAO: peroxisomal N 1 -acetyl-spermine/spermidine oxidase; SMOX, spermine oxidase. ( B ) Acetyl-CoA level in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. Cells from 4 separate experiments were stored at –80°C and then tested in a single plate. n = 4; 1-way ANOVA multiple comparisons (matched). ( C ) Dot blot of acetyl-lysine in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. The values of the quantification were normalized with the control samples. ( D ) Western blot of the samples in C . Acetylated histones and nonhistone proteins in the bracket areas were quantified separately and normalized with β-Actin level. All values were further normalized by the control samples. ( E ) Western blot of HA-tagged SAT1 overexpressed in HEK293T cells with PBA, MG132, or the combination treatment. The HA-SAT1 level was normalized with the β-Actin level. The values of the cells without HA-SAT1 plasmid transfection were set as background. All the values were further normalized by that of the cells with indicated treatment. ( F ) Western blot of SAT1 induced by DENSPM in patient fibroblasts (CMS1849a) with indicated treatment. The SAT1 level was normalized with the β-Actin level. Values of the cells without DENSPM treatment were set as background. All values were further normalized by that of cells with DENSPM and without PBA or MG132 treatment. Images in C – F are representative of 3 separate experiments. n =3; * P < 0.05, ** P < 0.01, *** P < 0.001; 1-way ANOVA multiple comparisons (matched). Data represent mean ± SEM.
Funano, A, supplied by TANAKA SCIENTIFIC LIMITED, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bioactive peptides derived from food sources and their use as bioactives in commercial products.
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Bioactive peptides derived from food sources and their use as bioactives in commercial products.
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Bioactive peptides derived from food sources and their use as bioactives in commercial products.
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Bioactive peptides derived from food sources and their use as bioactives in commercial products.
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Image Search Results


( A ) Diagram of the hypothesis of PBA-derived phenylacetyl-CoA competing with acetyl-CoA to interfere with SAT1-mediated polyamine catabolism and acetyl-CoA consumption. SPDSY, spermidine synthase; PAO: peroxisomal N 1 -acetyl-spermine/spermidine oxidase; SMOX, spermine oxidase. ( B ) Acetyl-CoA level in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. Cells from 4 separate experiments were stored at –80°C and then tested in a single plate. n = 4; 1-way ANOVA multiple comparisons (matched). ( C ) Dot blot of acetyl-lysine in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. The values of the quantification were normalized with the control samples. ( D ) Western blot of the samples in C . Acetylated histones and nonhistone proteins in the bracket areas were quantified separately and normalized with β-Actin level. All values were further normalized by the control samples. ( E ) Western blot of HA-tagged SAT1 overexpressed in HEK293T cells with PBA, MG132, or the combination treatment. The HA-SAT1 level was normalized with the β-Actin level. The values of the cells without HA-SAT1 plasmid transfection were set as background. All the values were further normalized by that of the cells with indicated treatment. ( F ) Western blot of SAT1 induced by DENSPM in patient fibroblasts (CMS1849a) with indicated treatment. The SAT1 level was normalized with the β-Actin level. Values of the cells without DENSPM treatment were set as background. All values were further normalized by that of cells with DENSPM and without PBA or MG132 treatment. Images in C – F are representative of 3 separate experiments. n =3; * P < 0.05, ** P < 0.01, *** P < 0.001; 1-way ANOVA multiple comparisons (matched). Data represent mean ± SEM.

Journal: JCI Insight

Article Title: Phenylbutyrate modulates polyamine acetylase and ameliorates Snyder-Robinson syndrome in a Drosophila model and patient cells

doi: 10.1172/jci.insight.158457

Figure Lengend Snippet: ( A ) Diagram of the hypothesis of PBA-derived phenylacetyl-CoA competing with acetyl-CoA to interfere with SAT1-mediated polyamine catabolism and acetyl-CoA consumption. SPDSY, spermidine synthase; PAO: peroxisomal N 1 -acetyl-spermine/spermidine oxidase; SMOX, spermine oxidase. ( B ) Acetyl-CoA level in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. Cells from 4 separate experiments were stored at –80°C and then tested in a single plate. n = 4; 1-way ANOVA multiple comparisons (matched). ( C ) Dot blot of acetyl-lysine in HEK293T cells with SAT1 overexpression with or without 2 mM PBA treatment. The values of the quantification were normalized with the control samples. ( D ) Western blot of the samples in C . Acetylated histones and nonhistone proteins in the bracket areas were quantified separately and normalized with β-Actin level. All values were further normalized by the control samples. ( E ) Western blot of HA-tagged SAT1 overexpressed in HEK293T cells with PBA, MG132, or the combination treatment. The HA-SAT1 level was normalized with the β-Actin level. The values of the cells without HA-SAT1 plasmid transfection were set as background. All the values were further normalized by that of the cells with indicated treatment. ( F ) Western blot of SAT1 induced by DENSPM in patient fibroblasts (CMS1849a) with indicated treatment. The SAT1 level was normalized with the β-Actin level. Values of the cells without DENSPM treatment were set as background. All values were further normalized by that of cells with DENSPM and without PBA or MG132 treatment. Images in C – F are representative of 3 separate experiments. n =3; * P < 0.05, ** P < 0.01, *** P < 0.001; 1-way ANOVA multiple comparisons (matched). Data represent mean ± SEM.

Article Snippet: The SAT1 CDS was amplified from Addgene plasmid 25493 (a gift from Cheryl Arrowsmith, University Health Network, Toronto, Ontario, Canada).

Techniques: Derivative Assay, Over Expression, Dot Blot, Control, Western Blot, Plasmid Preparation, Transfection

Bioactive peptides derived from food sources and their use as bioactives in commercial products.

Journal: International Journal of Molecular Sciences

Article Title: Bioactive Carbohydrates and Peptides in Foods: An Overview of Sources, Downstream Processing Steps and Associated Bioactivities

doi: 10.3390/ijms160922485

Figure Lengend Snippet: Bioactive peptides derived from food sources and their use as bioactives in commercial products.

Article Snippet: VY , Antihypertensive , Sato Marine Super P , Sato Pharmaceutical Co., Ltd., Tokyo, Japan , Tablet , Sardine , [ ] .

Techniques: Derivative Assay, Sequencing, Capsules, Control, Cream