sodium l-ascorbate Search Results


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  • 95
    Millipore sodium l ascorbate
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Sodium L Ascorbate, supplied by Millipore, used in various techniques. Bioz Stars score: 95/100, based on 336 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    PeproTech pdgf ascorbic acid
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Pdgf Ascorbic Acid, supplied by PeproTech, used in various techniques. Bioz Stars score: 92/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    84
    Santa Cruz Biotechnology sodium l ascorbate
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Sodium L Ascorbate, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 84/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    84
    TCI Tokyo Chemical Industry sodium l ascorbate
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Sodium L Ascorbate, supplied by TCI Tokyo Chemical Industry, used in various techniques. Bioz Stars score: 84/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    84
    Applichem sodium l ascorbate
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Sodium L Ascorbate, supplied by Applichem, used in various techniques. Bioz Stars score: 84/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    87
    Millipore 5x10 5 m sodium l ascorbate
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    5x10 5 M Sodium L Ascorbate, supplied by Millipore, used in various techniques. Bioz Stars score: 87/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    76
    Millipore sigma sodium l ascorbate cat no
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Sigma Sodium L Ascorbate Cat No, supplied by Millipore, used in various techniques. Bioz Stars score: 76/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    78
    Thermo Fisher l ascorbate acid sodium salt
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    L Ascorbate Acid Sodium Salt, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 78/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    95
    Millipore sodium ascorbate
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Sodium Ascorbate, supplied by Millipore, used in various techniques. Bioz Stars score: 95/100, based on 809 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    81
    Tocris sodium ascorbate
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Sodium Ascorbate, supplied by Tocris, used in various techniques. Bioz Stars score: 81/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    90
    Thermo Fisher reaction buffer
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Reaction Buffer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 5752 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    90
    Thermo Fisher click it reaction buffer
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Click It Reaction Buffer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 101 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    87
    Millipore 10 undecynoic acid
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    10 Undecynoic Acid, supplied by Millipore, used in various techniques. Bioz Stars score: 87/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    79
    Millipore ascorbic acid 2phosphate
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Ascorbic Acid 2phosphate, supplied by Millipore, used in various techniques. Bioz Stars score: 79/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    86
    Millipore mmol ascorbic acid
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Mmol Ascorbic Acid, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    78
    Millipore 50 m ascorbic acid
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    50 M Ascorbic Acid, supplied by Millipore, used in various techniques. Bioz Stars score: 78/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Lonza egm 2 bullet kit
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Egm 2 Bullet Kit, supplied by Lonza, used in various techniques. Bioz Stars score: 99/100, based on 482 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    SAS institute vitamin c sas
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Vitamin C Sas, supplied by SAS institute, used in various techniques. Bioz Stars score: 75/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Supelco constructedwith l ascorbic acid
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Constructedwith L Ascorbic Acid, supplied by Supelco, used in various techniques. Bioz Stars score: 79/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    76
    Merck KGaA ascorbic acid reflectoquant
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Ascorbic Acid Reflectoquant, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 76/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    79
    STEMCELL Technologies Inc ascorbic acid 2 phospate
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
    Ascorbic Acid 2 Phospate, supplied by STEMCELL Technologies Inc, used in various techniques. Bioz Stars score: 79/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore magnisum l ascorbic acid phosphate
    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
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    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P
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    Ascorbic acid 6-palmitate and salmon sperm protamine act as broad-spectrum anti-toxins. ( a ) Ascorbic acid 6-palmitate and salmon sperm protamine were tested for their ability to inhibit LF-PA83-mediated cytotoxicity. RAW264.7 cells were seeded at 1 × 10 4  cells/well on 96-well plates and the following day were incubated with indicated doses of drugs for 1 hour, followed by 3 hours intoxication with 0.5 μg/ml PA83 + LF. ( b ) Sixteen μM of salmon sperm protamine reduces cellular sensitivity to LF + PA63. RAW264.7 cells were pretreated either with DMSO or with protamine for 1 hour, and then treated with 0.5 μg/ml of LF and PA63 for 6 hours. Averages, standard deviations, and  P  values are shown for each condition. ( c,d ) Ascorbic acid 6-palmitate and salmon sperm protamine were tested for their ability to inhibit cytotoxicities mediated by  Pseudomonas aeruginosa  exotoxin A and Cholera toxin. RAW264.7 cells were seeded at 1 × 10 4  cells/well on 96-well plates and the following day were incubated with indicated doses of drugs for 1 hour, followed by 12 hours intoxication with 2 and 4 μg/ml of  Pseudomonas  ( c ) and Cholera ( d ) toxins respectively. Cell viability was determined by MTT assay (Materials and Methods) and is shown as the percentage of survivors relative to cells not treated with drugs. Averages, standard deviations, and  P  values are shown for each condition. Each  P  value represents a comparison of drug-treatment condition to a condition without drugs.
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    Ascorbic acid 6-palmitate and salmon sperm protamine act as broad-spectrum anti-toxins. ( a ) Ascorbic acid 6-palmitate and salmon sperm protamine were tested for their ability to inhibit LF-PA83-mediated cytotoxicity. RAW264.7 cells were seeded at 1 × 10 4  cells/well on 96-well plates and the following day were incubated with indicated doses of drugs for 1 hour, followed by 3 hours intoxication with 0.5 μg/ml PA83 + LF. ( b ) Sixteen μM of salmon sperm protamine reduces cellular sensitivity to LF + PA63. RAW264.7 cells were pretreated either with DMSO or with protamine for 1 hour, and then treated with 0.5 μg/ml of LF and PA63 for 6 hours. Averages, standard deviations, and  P  values are shown for each condition. ( c,d ) Ascorbic acid 6-palmitate and salmon sperm protamine were tested for their ability to inhibit cytotoxicities mediated by  Pseudomonas aeruginosa  exotoxin A and Cholera toxin. RAW264.7 cells were seeded at 1 × 10 4  cells/well on 96-well plates and the following day were incubated with indicated doses of drugs for 1 hour, followed by 12 hours intoxication with 2 and 4 μg/ml of  Pseudomonas  ( c ) and Cholera ( d ) toxins respectively. Cell viability was determined by MTT assay (Materials and Methods) and is shown as the percentage of survivors relative to cells not treated with drugs. Averages, standard deviations, and  P  values are shown for each condition. Each  P  value represents a comparison of drug-treatment condition to a condition without drugs.
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    Uptake of [ 14 C] AA in presence of L-ascorbic acid (L-AA), D-isoascorbic acid (D-Iso AA), <t>dehydro</t> ascorbic acid <t>(DHAA),</t> D-glucose and para-amino hippuric acid (PAHA) at three different concentrations across HCEC and D407 Cells. [ 14 C] AA uptake was performed
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    Triangle Biosystems tbsia
    Uptake of [ 14 C] AA in presence of L-ascorbic acid (L-AA), D-isoascorbic acid (D-Iso AA), <t>dehydro</t> ascorbic acid <t>(DHAA),</t> D-glucose and para-amino hippuric acid (PAHA) at three different concentrations across HCEC and D407 Cells. [ 14 C] AA uptake was performed
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    Millipore 2 phospho vitamin c pvitc
    Uptake of [ 14 C] AA in presence of L-ascorbic acid (L-AA), D-isoascorbic acid (D-Iso AA), <t>dehydro</t> ascorbic acid <t>(DHAA),</t> D-glucose and para-amino hippuric acid (PAHA) at three different concentrations across HCEC and D407 Cells. [ 14 C] AA uptake was performed
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    Uptake of [ 14 C] AA in presence of L-ascorbic acid (L-AA), D-isoascorbic acid (D-Iso AA), <t>dehydro</t> ascorbic acid <t>(DHAA),</t> D-glucose and para-amino hippuric acid (PAHA) at three different concentrations across HCEC and D407 Cells. [ 14 C] AA uptake was performed
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    Image Search Results


    APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2  were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P

    Journal: EMBO Reports

    Article Title: Restoration of 5‐hydroxymethylcytosine by ascorbate blocks kidney tumour growth

    doi: 10.15252/embr.201745401

    Figure Lengend Snippet: APM significantly increases 5hmC levels at physiological concentrations but with decreased cell damage compared with AsANa Dot blot assays of 5hmC levels upon vitamin C treatment in ccRCC cell lines (786‐O, A498). AsANa represents sodium L‐ascorbate, and APM represents L‐ascorbic acid 2‐phosphate sesquimagnesium. Dot blot assays of 5hmC levels upon vitamin C treatment at physiological concentrations. 769‐P is a ccRCC cell line. Dot blot assays of 5hmC and 5mC levels in 786‐O and A498 ccRCC cells and HK‐2 cells. The cells were treated for 24 h with 250 μM vitamin C. Cell viability was evaluated using the MTS assay after the addition of vitamin C for 48 h. Cell apoptosis was analysed by flow cytometry with Annexin V and PI staining. 786‐O cells were treated with vitamin C for 24 h. Extracellular concentrations of H 2 O 2 were measured with or without vitamin C treatment at the indicated concentrations. Cells treated with catalase were used as a positive control. * P

    Article Snippet: The cells were cultured with sodium L‐ascorbate (Sigma, #A4034) or L‐ascorbic APM (Sigma, #A8960) as indicated.

    Techniques: Dot Blot, MTS Assay, Flow Cytometry, Cytometry, Staining, Positive Control

    Ascorbic acid 6-palmitate and salmon sperm protamine act as broad-spectrum anti-toxins. ( a ) Ascorbic acid 6-palmitate and salmon sperm protamine were tested for their ability to inhibit LF-PA83-mediated cytotoxicity. RAW264.7 cells were seeded at 1 × 10 4  cells/well on 96-well plates and the following day were incubated with indicated doses of drugs for 1 hour, followed by 3 hours intoxication with 0.5 μg/ml PA83 + LF. ( b ) Sixteen μM of salmon sperm protamine reduces cellular sensitivity to LF + PA63. RAW264.7 cells were pretreated either with DMSO or with protamine for 1 hour, and then treated with 0.5 μg/ml of LF and PA63 for 6 hours. Averages, standard deviations, and  P  values are shown for each condition. ( c,d ) Ascorbic acid 6-palmitate and salmon sperm protamine were tested for their ability to inhibit cytotoxicities mediated by  Pseudomonas aeruginosa  exotoxin A and Cholera toxin. RAW264.7 cells were seeded at 1 × 10 4  cells/well on 96-well plates and the following day were incubated with indicated doses of drugs for 1 hour, followed by 12 hours intoxication with 2 and 4 μg/ml of  Pseudomonas  ( c ) and Cholera ( d ) toxins respectively. Cell viability was determined by MTT assay (Materials and Methods) and is shown as the percentage of survivors relative to cells not treated with drugs. Averages, standard deviations, and  P  values are shown for each condition. Each  P  value represents a comparison of drug-treatment condition to a condition without drugs.

    Journal: Scientific Reports

    Article Title: Cross-inhibition of pathogenic agents and the host proteins they exploit

    doi: 10.1038/srep34846

    Figure Lengend Snippet: Ascorbic acid 6-palmitate and salmon sperm protamine act as broad-spectrum anti-toxins. ( a ) Ascorbic acid 6-palmitate and salmon sperm protamine were tested for their ability to inhibit LF-PA83-mediated cytotoxicity. RAW264.7 cells were seeded at 1 × 10 4 cells/well on 96-well plates and the following day were incubated with indicated doses of drugs for 1 hour, followed by 3 hours intoxication with 0.5 μg/ml PA83 + LF. ( b ) Sixteen μM of salmon sperm protamine reduces cellular sensitivity to LF + PA63. RAW264.7 cells were pretreated either with DMSO or with protamine for 1 hour, and then treated with 0.5 μg/ml of LF and PA63 for 6 hours. Averages, standard deviations, and P values are shown for each condition. ( c,d ) Ascorbic acid 6-palmitate and salmon sperm protamine were tested for their ability to inhibit cytotoxicities mediated by Pseudomonas aeruginosa exotoxin A and Cholera toxin. RAW264.7 cells were seeded at 1 × 10 4 cells/well on 96-well plates and the following day were incubated with indicated doses of drugs for 1 hour, followed by 12 hours intoxication with 2 and 4 μg/ml of Pseudomonas ( c ) and Cholera ( d ) toxins respectively. Cell viability was determined by MTT assay (Materials and Methods) and is shown as the percentage of survivors relative to cells not treated with drugs. Averages, standard deviations, and P values are shown for each condition. Each P value represents a comparison of drug-treatment condition to a condition without drugs.

    Article Snippet: Salmon sperm protamine, cetylpyridinium bromide, domiphen bromide, cetalkonium chloride, sodium lauryl sulfate, ascorbic acid 6-palmitate, sodium dodecylbenzenesulfonate, docusate sodium, and candesartan cilexetil were purchased from Sigma-Aldrich (St. Louis, MO, USA).

    Techniques: Activated Clotting Time Assay, Incubation, MTT Assay

    Uptake of [ 14 C] AA in presence of L-ascorbic acid (L-AA), D-isoascorbic acid (D-Iso AA), dehydro ascorbic acid (DHAA), D-glucose and para-amino hippuric acid (PAHA) at three different concentrations across HCEC and D407 Cells. [ 14 C] AA uptake was performed

    Journal: Current eye research

    Article Title: Functional Characterization and Molecular Identification of Vitamin C Transporter (SVCT2) in Human Corneal Epithelial (HCEC) and Retinal Pigment Epithelial (D407) Cells

    doi: 10.3109/02713683.2014.935443

    Figure Lengend Snippet: Uptake of [ 14 C] AA in presence of L-ascorbic acid (L-AA), D-isoascorbic acid (D-Iso AA), dehydro ascorbic acid (DHAA), D-glucose and para-amino hippuric acid (PAHA) at three different concentrations across HCEC and D407 Cells. [ 14 C] AA uptake was performed

    Article Snippet: Unlabeled L-ascorbic acid, D-iso-ascorbic acid, dehydro-ascorbic acid (DHAA), glucose, para-amino hippuric acid (PAHA), sodium azide, ouabain, 2,4-dinitrophenol, choline chloride, HEPES, bovine insulin, human epidermal growth factor, Triton X-100, phorbol-12-myristate-13-acetate (PMA), bisindolylmaleimide I (BIS), 3-isobutyl-1-methyl-xanthine (IBMX), 4,4′-di-isothiocyanatostilbene-2,2′-disulphonic acid (DIDS), 4-acetamido-4′-isothiocya-nostilbene-2,2′-disulfonic acid (SITC) and D-glucose were purchased from Sigma Chemical Co (St. Louis, MO).

    Techniques: