densitometer gs-800 scanner Search Results


hpetm coomassie® staining kit  (SERVA Electrophoresis)
90
SERVA Electrophoresis hpetm coomassie® staining kit
Hpetm Coomassie® Staining Kit, supplied by SERVA Electrophoresis, 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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Average 90 stars, based on 1 article reviews
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fuji fla-3000 scanner  (FUJIFILM)
90
FUJIFILM fuji fla-3000 scanner
Fuji Fla 3000 Scanner, supplied by FUJIFILM, 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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Average 90 stars, based on 1 article reviews
fuji fla-3000 scanner - by Bioz Stars, 2026-09
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colloidal coomassie stained sds page gels  (Bio-Rad)
98
Bio-Rad colloidal coomassie stained sds page gels
Colloidal Coomassie Stained Sds Page Gels, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 98 stars, based on 1 article reviews
colloidal coomassie stained sds page gels - by Bioz Stars, 2026-09
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coomassie brilliant blue r 250  (Bio-Rad)
96
Bio-Rad coomassie brilliant blue r 250
Coomassie Brilliant Blue R 250, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
coomassie brilliant blue r 250 - by Bioz Stars, 2026-09
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reagent  (Bio-Rad)
96
Bio-Rad reagent
Reagent, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
reagent - by Bioz Stars, 2026-09
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coomassie brilliant blue g 250  (Bio-Rad)
96
Bio-Rad coomassie brilliant blue g 250
Coomassie Brilliant Blue G 250, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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coomassie brilliant blue staining  (Bio-Rad)
99
Bio-Rad coomassie brilliant blue staining
FIG. 4. Degradation of -toxin and -toxoid by spent B. subtilis supernatants. Lactococcus lactis-produced -toxin and -toxoid cul- tures were incubated with spent supernatants of stationary-phase cul- tures of B. subtilis strains 168 and WB800. As a control, TY medium was used. (A) Typical <t>Coomassie</t> brilliant blue-stained polyacrylamide gel showing results of the degradation assay. The incubation time (T) in minutes is indicated. Left lanes show -toxoid and -toxin exposed to strain 168 culture supernatant; right lanes show -toxoid and -toxin exposed to strain WB800 culture supernatant. M, protein marker, 35-kDa band. (B) The amount of -toxin/-toxoid measured after 10 min was set to 100%. The remaining amounts of -toxoid and -toxin after 1 h were determined and plotted. Experiments were performed in duplicate; error bars depict standard errors.
Coomassie Brilliant Blue Staining, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/densitometer+gs-800+scanner/Coomassie+Brilliant+Blue+R-250+Staining+Solution/10__1128_slash_aem__02356___06-116-9-17
Average 99 stars, based on 1 article reviews
coomassie brilliant blue staining - by Bioz Stars, 2026-09
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bio rad mes running buffer  (Bio-Rad)
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Bio-Rad bio rad mes running buffer
FIG. 4. Degradation of -toxin and -toxoid by spent B. subtilis supernatants. Lactococcus lactis-produced -toxin and -toxoid cul- tures were incubated with spent supernatants of stationary-phase cul- tures of B. subtilis strains 168 and WB800. As a control, TY medium was used. (A) Typical <t>Coomassie</t> brilliant blue-stained polyacrylamide gel showing results of the degradation assay. The incubation time (T) in minutes is indicated. Left lanes show -toxoid and -toxin exposed to strain 168 culture supernatant; right lanes show -toxoid and -toxin exposed to strain WB800 culture supernatant. M, protein marker, 35-kDa band. (B) The amount of -toxin/-toxoid measured after 10 min was set to 100%. The remaining amounts of -toxoid and -toxin after 1 h were determined and plotted. Experiments were performed in duplicate; error bars depict standard errors.
Bio Rad Mes Running Buffer, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/densitometer+gs-800+scanner/XT+MES+Running+Buffer/10__1094_slash_phyto___11___13___0317___r-166-31-31
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bio safe coomassie stain  (Bio-Rad)
96
Bio-Rad bio safe coomassie stain
FIG. 4. Degradation of -toxin and -toxoid by spent B. subtilis supernatants. Lactococcus lactis-produced -toxin and -toxoid cul- tures were incubated with spent supernatants of stationary-phase cul- tures of B. subtilis strains 168 and WB800. As a control, TY medium was used. (A) Typical <t>Coomassie</t> brilliant blue-stained polyacrylamide gel showing results of the degradation assay. The incubation time (T) in minutes is indicated. Left lanes show -toxoid and -toxin exposed to strain 168 culture supernatant; right lanes show -toxoid and -toxin exposed to strain WB800 culture supernatant. M, protein marker, 35-kDa band. (B) The amount of -toxin/-toxoid measured after 10 min was set to 100%. The remaining amounts of -toxoid and -toxin after 1 h were determined and plotted. Experiments were performed in duplicate; error bars depict standard errors.
Bio Safe Coomassie Stain, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/densitometer+gs-800+scanner/Bio-Safe+Coomassie+Stain/pmc03293479-129-6-9
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bis tris precast gels  (Bio-Rad)
98
Bio-Rad bis tris precast gels
FIG. 4. Degradation of -toxin and -toxoid by spent B. subtilis supernatants. Lactococcus lactis-produced -toxin and -toxoid cul- tures were incubated with spent supernatants of stationary-phase cul- tures of B. subtilis strains 168 and WB800. As a control, TY medium was used. (A) Typical <t>Coomassie</t> brilliant blue-stained polyacrylamide gel showing results of the degradation assay. The incubation time (T) in minutes is indicated. Left lanes show -toxoid and -toxin exposed to strain 168 culture supernatant; right lanes show -toxoid and -toxin exposed to strain WB800 culture supernatant. M, protein marker, 35-kDa band. (B) The amount of -toxin/-toxoid measured after 10 min was set to 100%. The remaining amounts of -toxoid and -toxin after 1 h were determined and plotted. Experiments were performed in duplicate; error bars depict standard errors.
Bis Tris Precast Gels, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/densitometer+gs-800+scanner/Tris/10__1094_slash_phyto___11___13___0317___r-166-26-31
Average 98 stars, based on 1 article reviews
bis tris precast gels - by Bioz Stars, 2026-09
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li cor odyssey clx scanner  (LI-COR)
99
LI-COR li cor odyssey clx scanner
FIG. 4. Degradation of -toxin and -toxoid by spent B. subtilis supernatants. Lactococcus lactis-produced -toxin and -toxoid cul- tures were incubated with spent supernatants of stationary-phase cul- tures of B. subtilis strains 168 and WB800. As a control, TY medium was used. (A) Typical <t>Coomassie</t> brilliant blue-stained polyacrylamide gel showing results of the degradation assay. The incubation time (T) in minutes is indicated. Left lanes show -toxoid and -toxin exposed to strain 168 culture supernatant; right lanes show -toxoid and -toxin exposed to strain WB800 culture supernatant. M, protein marker, 35-kDa band. (B) The amount of -toxin/-toxoid measured after 10 min was set to 100%. The remaining amounts of -toxoid and -toxin after 1 h were determined and plotted. Experiments were performed in duplicate; error bars depict standard errors.
Li Cor Odyssey Clx Scanner, supplied by LI-COR, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


FIG. 4. Degradation of -toxin and -toxoid by spent B. subtilis supernatants. Lactococcus lactis-produced -toxin and -toxoid cul- tures were incubated with spent supernatants of stationary-phase cul- tures of B. subtilis strains 168 and WB800. As a control, TY medium was used. (A) Typical Coomassie brilliant blue-stained polyacrylamide gel showing results of the degradation assay. The incubation time (T) in minutes is indicated. Left lanes show -toxoid and -toxin exposed to strain 168 culture supernatant; right lanes show -toxoid and -toxin exposed to strain WB800 culture supernatant. M, protein marker, 35-kDa band. (B) The amount of -toxin/-toxoid measured after 10 min was set to 100%. The remaining amounts of -toxoid and -toxin after 1 h were determined and plotted. Experiments were performed in duplicate; error bars depict standard errors.

Journal: Applied and Environmental Microbiology

Article Title: Changing a Single Amino Acid in Clostridium perfringens β-Toxin Affects the Efficiency of Heterologous Secretion by Bacillus subtilis

doi: 10.1128/aem.02356-06

Figure Lengend Snippet: FIG. 4. Degradation of -toxin and -toxoid by spent B. subtilis supernatants. Lactococcus lactis-produced -toxin and -toxoid cul- tures were incubated with spent supernatants of stationary-phase cul- tures of B. subtilis strains 168 and WB800. As a control, TY medium was used. (A) Typical Coomassie brilliant blue-stained polyacrylamide gel showing results of the degradation assay. The incubation time (T) in minutes is indicated. Left lanes show -toxoid and -toxin exposed to strain 168 culture supernatant; right lanes show -toxoid and -toxin exposed to strain WB800 culture supernatant. M, protein marker, 35-kDa band. (B) The amount of -toxin/-toxoid measured after 10 min was set to 100%. The remaining amounts of -toxoid and -toxin after 1 h were determined and plotted. Experiments were performed in duplicate; error bars depict standard errors.

Article Snippet: The concentrations of -toxin and -toxoid were determined by Coomassie brilliant blue staining followed by densitometric scanning (Bio-Rad GS-800 scanner) and analysis with Quantity One software (Bio-Rad, Hercules, CA).

Techniques: Produced, Incubation, Control, Staining, Degradation Assay, Marker

FIG. 5. Secretion and secretion stress of -toxin, -toxoid, and intermediate mutants. (A) Coomassie brilliant blue-stained 12% SDS- polyacrylamide gel containing 10 concentrated supernatant of B. subtilis strain NZ8900 1.5 h after induction of the inducible tox plasmids. (B) The average PhtrA-GFP expression per cell in arbitrary units, measured 1.5 h after induction, is shown. Experiments were performed in duplicate; error bars depict standard errors. DDK, WT -toxin (D54DK); AAA, -toxoid (A54AA); all other intermediate mutants (mut) are likewise indicated.

Journal: Applied and Environmental Microbiology

Article Title: Changing a Single Amino Acid in Clostridium perfringens β-Toxin Affects the Efficiency of Heterologous Secretion by Bacillus subtilis

doi: 10.1128/aem.02356-06

Figure Lengend Snippet: FIG. 5. Secretion and secretion stress of -toxin, -toxoid, and intermediate mutants. (A) Coomassie brilliant blue-stained 12% SDS- polyacrylamide gel containing 10 concentrated supernatant of B. subtilis strain NZ8900 1.5 h after induction of the inducible tox plasmids. (B) The average PhtrA-GFP expression per cell in arbitrary units, measured 1.5 h after induction, is shown. Experiments were performed in duplicate; error bars depict standard errors. DDK, WT -toxin (D54DK); AAA, -toxoid (A54AA); all other intermediate mutants (mut) are likewise indicated.

Article Snippet: The concentrations of -toxin and -toxoid were determined by Coomassie brilliant blue staining followed by densitometric scanning (Bio-Rad GS-800 scanner) and analysis with Quantity One software (Bio-Rad, Hercules, CA).

Techniques: Staining, Expressing