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DeNovix fluorometer ds 11 fx
Fluorometer Ds 11 Fx, supplied by DeNovix, used in various techniques. Bioz Stars score: 97/100, based on 1075 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/spectrophotometer+fluorometer/Microvolume+Spectrophotometer+And+Fluorometer+DeNovix+DS-11+FX/pmc13179062-313-8-12
Average 97 stars, based on 1075 article reviews
fluorometer ds 11 fx - by Bioz Stars, 2026-10
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Spectrophotometry:

Article Title: Assessment of nucleic acid extraction protocols for antibiotic resistance genes (ARGs) quantification in aircraft wastewater
Article Snippet: After homogenization, nucleic acid extraction was completed as per the Qiagen AllPrep PowerViral DNA/RNA Kit (Qiagen) instructions except elution was performed with 200 μL of RNase-free water to match the elution volume of the DNeasy Blood and Tissue Kit (Qiagen). .. The concentrations of extracted DNA were determined by a DeNovix Spectrophotometer/Fluorometer (DeNovix DS-11, Wilmington, USA). ..

Article Title: Priming from within: TLR2 dependent but receptor independent activation of the mammary macrophage inflammasome by Streptococcus uberis
Article Snippet: .. The RNA pellets were subsequently dried, resuspended in RNase free water and the concentration determined and adjusted to approximately 15 ng/μL using a spectrophotometer/fluorometer (Denovix, DS-11 FX+). .. RT qRT-PCR of the RNA was completed using Luna ® Universal One-Step RT-qPCR Kit with the primers (Sigma) listed in (10 μM in DNase free water).

Article Title: Root-associated Streptomyces produce galbonolides to modulate plant immunity and promote rhizosphere colonization.
Article Snippet: The total microbe DNA from 100 mg of bulk or rhizosphere samples 186 was extracted using the Quick-DNA Fecal/Soil Microbe Miniprep kit (Zymo Research) following 187 manufacturer’s instructions. .. DNA was eluted in 100 μL DNA Elution Buffer, quantified with DS-11 188 Spectrophotometer/Fluorometer (DeNovix), and stored at -80°C until processing. ..

Article Title: Priming from within: TLR2 dependent but receptor independent activation of the mammary macrophage inflammasome by Streptococcus uberis
Article Snippet: .. Concentration of the rSUB1154 proteins were determined using a spectrophotometer/fluorometer (Denovix, DS-11 FX+) and stored with 10% glycerol (Fisher Chemical, G/0650/08) at -80°C. ..

Article Title: Curbing Breast Cancer by Altering V-ATPase Action on F-Actin, Heterochromatin, ETV7 and mTORC2 Signaling.
Article Snippet: After trypsinization, cells were lysed with Pierce lysis buffer (87788, ThermoFisher Scientific) with Halt’s protease and phosphatase inhibitor cocktail (78440, ThermoFisher Scientific) following the manufacturer’s instructions. .. Protein concentrations were determined using the Pierce 660 colorimetric assay (22660, ThermoFisher Scientific) and a spectrophotometer/fluorometer (DeNovix, DS11 FX+, USA) using the nano drop function at 280 nm and was calibrated with dilutions of BSA standard (2 mg/ml, 500-0206, Bio-Rad). .. 40 μg of protein was diluted in 4x laemmli sample buffer (1610747, Bio-Rad) with β-mercaptoethanol (1610710, Bio-Rad), placed in 4-20% gradient acrylamide gels (456-8094, Bio- Rad), and separated by electrophoresis.

Article Title: Functional requirement for Dicer helicase arginine methylation in 26 G siRNA biogenesis and oocyte meiotic program.
Article Snippet: .. Afterwards, RNA samples were centrifuged briefly (10K RPM, 5 minutes, 4C) and concentrations and A260/280 ratios were determined using a Spectrophotometer/Fluorometer (DeNovix DS-11 FX+). ..

Article Title: A low-cost homogenizing device for in-field and remote DNA and RNA extraction
Article Snippet: .. DNA and RNA quantification: DNA and RNA concentrations were measured for each of the samples tested using a spectrophotometer/fluorometer (DeNovix, model DS-11FX, USA). ..

Article Title: A low-cost homogenizing device for in-field and remote DNA and RNA extraction
Article Snippet: Environmental monitoring of microorganisms is critical for the protection and enhancement of human and ecosystem health.. Even though these molecular methods have overtaken traditional culture-based methods and become more accessible, these techniques still require expensive equipment and dedicated facilities to process samples which in the context of a global pandemic, remote sampling areas or low-income countries can be extremely challenging.. Sample preparation and sample homogenisation are critical steps for molecular-based techniques, especially for the extraction of DNA and RNA.

Concentration Assay:

Article Title: Priming from within: TLR2 dependent but receptor independent activation of the mammary macrophage inflammasome by Streptococcus uberis
Article Snippet: .. The RNA pellets were subsequently dried, resuspended in RNase free water and the concentration determined and adjusted to approximately 15 ng/μL using a spectrophotometer/fluorometer (Denovix, DS-11 FX+). .. RT qRT-PCR of the RNA was completed using Luna ® Universal One-Step RT-qPCR Kit with the primers (Sigma) listed in (10 μM in DNase free water).

Article Title: Priming from within: TLR2 dependent but receptor independent activation of the mammary macrophage inflammasome by Streptococcus uberis
Article Snippet: .. Concentration of the rSUB1154 proteins were determined using a spectrophotometer/fluorometer (Denovix, DS-11 FX+) and stored with 10% glycerol (Fisher Chemical, G/0650/08) at -80°C. ..

Colorimetric Assay:

Article Title: Curbing Breast Cancer by Altering V-ATPase Action on F-Actin, Heterochromatin, ETV7 and mTORC2 Signaling.
Article Snippet: After trypsinization, cells were lysed with Pierce lysis buffer (87788, ThermoFisher Scientific) with Halt’s protease and phosphatase inhibitor cocktail (78440, ThermoFisher Scientific) following the manufacturer’s instructions. .. Protein concentrations were determined using the Pierce 660 colorimetric assay (22660, ThermoFisher Scientific) and a spectrophotometer/fluorometer (DeNovix, DS11 FX+, USA) using the nano drop function at 280 nm and was calibrated with dilutions of BSA standard (2 mg/ml, 500-0206, Bio-Rad). .. 40 μg of protein was diluted in 4x laemmli sample buffer (1610747, Bio-Rad) with β-mercaptoethanol (1610710, Bio-Rad), placed in 4-20% gradient acrylamide gels (456-8094, Bio- Rad), and separated by electrophoresis.



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Fluorometer Ds 11 Fx, supplied by DeNovix, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Rna, supplied by DeNovix, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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DeNovix spectrophotometer ds 11 fx
Spectrophotometer Ds 11 Fx, supplied by DeNovix, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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DeNovix absorption
a SnCE1 C256A AcK231 is neither deacetylated by human SIRT1 and SIRT2 nor by S. negevensis CobB, i.e., SnCobB. Deacetylation of acetylated wild type SnCE1 and site-specifically acetylated SnCE1 C256A AcK231 was assessed by immunoblotting with anti-acetyl lysine antibody (IB: AcK) and Coomassie Brilliant Blue staining was done as loading control (CBB). The experiment was performed in two independent technical replicates ( n = 2). Source data are provided as Source Data file. b SnCE1 C256A AcK231 elutes as monomer from analytic SEC column. Wild type SnCE1 elutes as monomer, SnCE1 C256A as tetramer. A 280 is the <t>absorption</t> at 280 nm. mAU: milli absorbance units. Fractions were analyzed by SDS-PAGE and gels were stained with Coomassie brilliant blue (CBB), immunoblotting with anti-acetyl-lysine antibody confirms the acetylation (IB: AcK) and staining with anti-SnCE1 antibody was done as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file. c SnCE1 C256A AcK231 is neither deacetylated by human sirtuins (SIRT1-SIRT7) nor by selected human classical HDACs. The acetylation state of SnCE1 was assessed by immunoblotting using an anti-acetyl lysine antibody (IB: AcK). Immunoblotting with anti-SnCE1 antibody served as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file.
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DeNovix ds 11 fx spectrophotometer
a SnCE1 C256A AcK231 is neither deacetylated by human SIRT1 and SIRT2 nor by S. negevensis CobB, i.e., SnCobB. Deacetylation of acetylated wild type SnCE1 and site-specifically acetylated SnCE1 C256A AcK231 was assessed by immunoblotting with anti-acetyl lysine antibody (IB: AcK) and Coomassie Brilliant Blue staining was done as loading control (CBB). The experiment was performed in two independent technical replicates ( n = 2). Source data are provided as Source Data file. b SnCE1 C256A AcK231 elutes as monomer from analytic SEC column. Wild type SnCE1 elutes as monomer, SnCE1 C256A as tetramer. A 280 is the <t>absorption</t> at 280 nm. mAU: milli absorbance units. Fractions were analyzed by SDS-PAGE and gels were stained with Coomassie brilliant blue (CBB), immunoblotting with anti-acetyl-lysine antibody confirms the acetylation (IB: AcK) and staining with anti-SnCE1 antibody was done as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file. c SnCE1 C256A AcK231 is neither deacetylated by human sirtuins (SIRT1-SIRT7) nor by selected human classical HDACs. The acetylation state of SnCE1 was assessed by immunoblotting using an anti-acetyl lysine antibody (IB: AcK). Immunoblotting with anti-SnCE1 antibody served as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file.
Ds 11 Fx Spectrophotometer, supplied by DeNovix, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/spectrophotometer+fluorometer/Microvolume+Spectrophotometer+And+Fluorometer+DeNovix+DS-11+FX/pmc13109719-94-6-9
Average 97 stars, based on 1 article reviews
ds 11 fx spectrophotometer - by Bioz Stars, 2026-10
97/100 stars
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DeNovix rna concentration
a SnCE1 C256A AcK231 is neither deacetylated by human SIRT1 and SIRT2 nor by S. negevensis CobB, i.e., SnCobB. Deacetylation of acetylated wild type SnCE1 and site-specifically acetylated SnCE1 C256A AcK231 was assessed by immunoblotting with anti-acetyl lysine antibody (IB: AcK) and Coomassie Brilliant Blue staining was done as loading control (CBB). The experiment was performed in two independent technical replicates ( n = 2). Source data are provided as Source Data file. b SnCE1 C256A AcK231 elutes as monomer from analytic SEC column. Wild type SnCE1 elutes as monomer, SnCE1 C256A as tetramer. A 280 is the <t>absorption</t> at 280 nm. mAU: milli absorbance units. Fractions were analyzed by SDS-PAGE and gels were stained with Coomassie brilliant blue (CBB), immunoblotting with anti-acetyl-lysine antibody confirms the acetylation (IB: AcK) and staining with anti-SnCE1 antibody was done as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file. c SnCE1 C256A AcK231 is neither deacetylated by human sirtuins (SIRT1-SIRT7) nor by selected human classical HDACs. The acetylation state of SnCE1 was assessed by immunoblotting using an anti-acetyl lysine antibody (IB: AcK). Immunoblotting with anti-SnCE1 antibody served as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file.
Rna Concentration, supplied by DeNovix, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/spectrophotometer+fluorometer/Microvolume+Spectrophotometer+And+Fluorometer+DeNovix+DS-11+FX/pmc13109719-94-0-9
Average 97 stars, based on 1 article reviews
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DeNovix sds washing solution
a SnCE1 C256A AcK231 is neither deacetylated by human SIRT1 and SIRT2 nor by S. negevensis CobB, i.e., SnCobB. Deacetylation of acetylated wild type SnCE1 and site-specifically acetylated SnCE1 C256A AcK231 was assessed by immunoblotting with anti-acetyl lysine antibody (IB: AcK) and Coomassie Brilliant Blue staining was done as loading control (CBB). The experiment was performed in two independent technical replicates ( n = 2). Source data are provided as Source Data file. b SnCE1 C256A AcK231 elutes as monomer from analytic SEC column. Wild type SnCE1 elutes as monomer, SnCE1 C256A as tetramer. A 280 is the <t>absorption</t> at 280 nm. mAU: milli absorbance units. Fractions were analyzed by SDS-PAGE and gels were stained with Coomassie brilliant blue (CBB), immunoblotting with anti-acetyl-lysine antibody confirms the acetylation (IB: AcK) and staining with anti-SnCE1 antibody was done as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file. c SnCE1 C256A AcK231 is neither deacetylated by human sirtuins (SIRT1-SIRT7) nor by selected human classical HDACs. The acetylation state of SnCE1 was assessed by immunoblotting using an anti-acetyl lysine antibody (IB: AcK). Immunoblotting with anti-SnCE1 antibody served as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file.
Sds Washing Solution, supplied by DeNovix, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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DeNovix peptide concentration
a SnCE1 C256A AcK231 is neither deacetylated by human SIRT1 and SIRT2 nor by S. negevensis CobB, i.e., SnCobB. Deacetylation of acetylated wild type SnCE1 and site-specifically acetylated SnCE1 C256A AcK231 was assessed by immunoblotting with anti-acetyl lysine antibody (IB: AcK) and Coomassie Brilliant Blue staining was done as loading control (CBB). The experiment was performed in two independent technical replicates ( n = 2). Source data are provided as Source Data file. b SnCE1 C256A AcK231 elutes as monomer from analytic SEC column. Wild type SnCE1 elutes as monomer, SnCE1 C256A as tetramer. A 280 is the <t>absorption</t> at 280 nm. mAU: milli absorbance units. Fractions were analyzed by SDS-PAGE and gels were stained with Coomassie brilliant blue (CBB), immunoblotting with anti-acetyl-lysine antibody confirms the acetylation (IB: AcK) and staining with anti-SnCE1 antibody was done as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file. c SnCE1 C256A AcK231 is neither deacetylated by human sirtuins (SIRT1-SIRT7) nor by selected human classical HDACs. The acetylation state of SnCE1 was assessed by immunoblotting using an anti-acetyl lysine antibody (IB: AcK). Immunoblotting with anti-SnCE1 antibody served as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file.
Peptide Concentration, supplied by DeNovix, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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DeNovix denovix ds 11 fx spectrophotometer fluorometer
a SnCE1 C256A AcK231 is neither deacetylated by human SIRT1 and SIRT2 nor by S. negevensis CobB, i.e., SnCobB. Deacetylation of acetylated wild type SnCE1 and site-specifically acetylated SnCE1 C256A AcK231 was assessed by immunoblotting with anti-acetyl lysine antibody (IB: AcK) and Coomassie Brilliant Blue staining was done as loading control (CBB). The experiment was performed in two independent technical replicates ( n = 2). Source data are provided as Source Data file. b SnCE1 C256A AcK231 elutes as monomer from analytic SEC column. Wild type SnCE1 elutes as monomer, SnCE1 C256A as tetramer. A 280 is the <t>absorption</t> at 280 nm. mAU: milli absorbance units. Fractions were analyzed by SDS-PAGE and gels were stained with Coomassie brilliant blue (CBB), immunoblotting with anti-acetyl-lysine antibody confirms the acetylation (IB: AcK) and staining with anti-SnCE1 antibody was done as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file. c SnCE1 C256A AcK231 is neither deacetylated by human sirtuins (SIRT1-SIRT7) nor by selected human classical HDACs. The acetylation state of SnCE1 was assessed by immunoblotting using an anti-acetyl lysine antibody (IB: AcK). Immunoblotting with anti-SnCE1 antibody served as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file.
Denovix Ds 11 Fx Spectrophotometer Fluorometer, supplied by DeNovix, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/spectrophotometer+fluorometer/Microvolume+Spectrophotometer+And+Fluorometer+DeNovix+DS-11+FX/bio_rxiv__64898__2026__04__22__720116-178-9-9
Average 97 stars, based on 1 article reviews
denovix ds 11 fx spectrophotometer fluorometer - by Bioz Stars, 2026-10
97/100 stars
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97
DeNovix spectrophotometer fluorometer
a SnCE1 C256A AcK231 is neither deacetylated by human SIRT1 and SIRT2 nor by S. negevensis CobB, i.e., SnCobB. Deacetylation of acetylated wild type SnCE1 and site-specifically acetylated SnCE1 C256A AcK231 was assessed by immunoblotting with anti-acetyl lysine antibody (IB: AcK) and Coomassie Brilliant Blue staining was done as loading control (CBB). The experiment was performed in two independent technical replicates ( n = 2). Source data are provided as Source Data file. b SnCE1 C256A AcK231 elutes as monomer from analytic SEC column. Wild type SnCE1 elutes as monomer, SnCE1 C256A as tetramer. A 280 is the <t>absorption</t> at 280 nm. mAU: milli absorbance units. Fractions were analyzed by SDS-PAGE and gels were stained with Coomassie brilliant blue (CBB), immunoblotting with anti-acetyl-lysine antibody confirms the acetylation (IB: AcK) and staining with anti-SnCE1 antibody was done as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file. c SnCE1 C256A AcK231 is neither deacetylated by human sirtuins (SIRT1-SIRT7) nor by selected human classical HDACs. The acetylation state of SnCE1 was assessed by immunoblotting using an anti-acetyl lysine antibody (IB: AcK). Immunoblotting with anti-SnCE1 antibody served as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file.
Spectrophotometer Fluorometer, supplied by DeNovix, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/spectrophotometer+fluorometer/Microvolume+Spectrophotometer+And+Fluorometer+DeNovix+DS-11+FX/pm42014716-699-20-21
Average 97 stars, based on 1 article reviews
spectrophotometer fluorometer - by Bioz Stars, 2026-10
97/100 stars
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Image Search Results


a SnCE1 C256A AcK231 is neither deacetylated by human SIRT1 and SIRT2 nor by S. negevensis CobB, i.e., SnCobB. Deacetylation of acetylated wild type SnCE1 and site-specifically acetylated SnCE1 C256A AcK231 was assessed by immunoblotting with anti-acetyl lysine antibody (IB: AcK) and Coomassie Brilliant Blue staining was done as loading control (CBB). The experiment was performed in two independent technical replicates ( n = 2). Source data are provided as Source Data file. b SnCE1 C256A AcK231 elutes as monomer from analytic SEC column. Wild type SnCE1 elutes as monomer, SnCE1 C256A as tetramer. A 280 is the absorption at 280 nm. mAU: milli absorbance units. Fractions were analyzed by SDS-PAGE and gels were stained with Coomassie brilliant blue (CBB), immunoblotting with anti-acetyl-lysine antibody confirms the acetylation (IB: AcK) and staining with anti-SnCE1 antibody was done as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file. c SnCE1 C256A AcK231 is neither deacetylated by human sirtuins (SIRT1-SIRT7) nor by selected human classical HDACs. The acetylation state of SnCE1 was assessed by immunoblotting using an anti-acetyl lysine antibody (IB: AcK). Immunoblotting with anti-SnCE1 antibody served as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file.

Journal: Nature Communications

Article Title: Reprogramming of bacterial virulence by lysine acetylation

doi: 10.1038/s41467-026-72244-8

Figure Lengend Snippet: a SnCE1 C256A AcK231 is neither deacetylated by human SIRT1 and SIRT2 nor by S. negevensis CobB, i.e., SnCobB. Deacetylation of acetylated wild type SnCE1 and site-specifically acetylated SnCE1 C256A AcK231 was assessed by immunoblotting with anti-acetyl lysine antibody (IB: AcK) and Coomassie Brilliant Blue staining was done as loading control (CBB). The experiment was performed in two independent technical replicates ( n = 2). Source data are provided as Source Data file. b SnCE1 C256A AcK231 elutes as monomer from analytic SEC column. Wild type SnCE1 elutes as monomer, SnCE1 C256A as tetramer. A 280 is the absorption at 280 nm. mAU: milli absorbance units. Fractions were analyzed by SDS-PAGE and gels were stained with Coomassie brilliant blue (CBB), immunoblotting with anti-acetyl-lysine antibody confirms the acetylation (IB: AcK) and staining with anti-SnCE1 antibody was done as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file. c SnCE1 C256A AcK231 is neither deacetylated by human sirtuins (SIRT1-SIRT7) nor by selected human classical HDACs. The acetylation state of SnCE1 was assessed by immunoblotting using an anti-acetyl lysine antibody (IB: AcK). Immunoblotting with anti-SnCE1 antibody served as loading control (IB: SnCE1). The experiment was performed once ( n = 1). Source data are provided as Source Data file.

Article Snippet: Elution fractions containing pure protein were pooled and concentrated before protein concentration was determined by measuring absorption at 280 nm using a spectrophotometer DS-11 FX (DeNovix, Wilmington USA).

Techniques: Western Blot, Staining, Control, SDS Page