typer version 4.0 software Search Results


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DNA Software Inc visual omp software version 7.5.1.0
Visual Omp Software Version 7.5.1.0, supplied by DNA Software 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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Ridom GmbH staphtype software (version 1.4
Staphtype Software (Version 1.4, supplied by Ridom 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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Sartorius AG incucyte s3 software
Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the <t>Incucyte</t> <t>S3</t> live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).
Incucyte S3 Software, supplied by Sartorius AG, 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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incucyte s3 software - by Bioz Stars, 2026-09
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Virco Pharmaceuticals vircotype hiv-1 version 4.1 software
Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the <t>Incucyte</t> <t>S3</t> live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).
Vircotype Hiv 1 Version 4.1 Software, supplied by Virco Pharmaceuticals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/typer+version+4%2E0+software/vircotype+hiv+1/pm20860529-47-7-12
Average 90 stars, based on 1 article reviews
vircotype hiv-1 version 4.1 software - by Bioz Stars, 2026-09
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Thermo Fisher pcr ssp
Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the <t>Incucyte</t> <t>S3</t> live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).
Pcr Ssp, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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STATA Corporation hiv status
Characteristics of women participating in qualitative exploration of lived <t> experiences </t> of water insecurity in Nyanza region, Kenya, by method (n=40)
Hiv Status, supplied by STATA Corporation, 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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STATA Corporation hiv care continuum close
Characteristics of women participating in qualitative exploration of lived <t> experiences </t> of water insecurity in Nyanza region, Kenya, by method (n=40)
Hiv Care Continuum Close, supplied by STATA Corporation, 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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Characteristics of women participating in qualitative exploration of lived <t> experiences </t> of water insecurity in Nyanza region, Kenya, by method (n=40)
3 Stream1 W2 Spss 100173 Restricted Zip 3 Stream1 W2 Stata 100173 Restricted Zip File Name File Type Notes 2 Stream1 W4 Csv 100175 General Zip, supplied by STATA Corporation, 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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STATA Corporation type i error rate
Characteristics of women participating in qualitative exploration of lived <t> experiences </t> of water insecurity in Nyanza region, Kenya, by method (n=40)
Type I Error Rate, supplied by STATA Corporation, 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


Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the Incucyte S3 live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).

Journal: Vaccines

Article Title: A Nanoscaffolded Spike-RBD Vaccine Provides Protection against SARS-CoV-2 with Minimal Anti-Scaffold Response

doi: 10.3390/vaccines9050431

Figure Lengend Snippet: Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the Incucyte S3 live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).

Article Snippet: The normalized GFP intensity was computed using the IncuCyte S3 software (Essen Bioscience; version 2019B Rev2, Sartorius, Göttingen, Germany) as integrated GFP intensity per well divided by the total area of the cells per well.

Techniques: Neutralization, Isolation, Affinity Chromatography, SDS Page, Binding Assay, Recombinant, Serial Dilution, Enzyme-linked Immunosorbent Assay, Purification, Adjuvant, MANN-WHITNEY, Virus, Infection, Transfection, Incubation, Control, Live Cell Imaging, Comparison, Labeling, Injection, Fluorescence, Derivative Assay, Two Tailed Test

Characteristics of women participating in qualitative exploration of lived  experiences  of water insecurity in Nyanza region, Kenya, by method (n=40)

Journal: Global public health

Article Title: “I know how stressful it is to lack water!” Exploring the lived experiences of household water insecurity among pregnant and postpartum women in western Kenya

doi: 10.1080/17441692.2018.1521861

Figure Lengend Snippet: Characteristics of women participating in qualitative exploration of lived experiences of water insecurity in Nyanza region, Kenya, by method (n=40)

Article Snippet: Differences in experiences by HIV status were tabulated using chi-square, t -tests, and Fisher’s exact tests in Stata 14.0 (StataCorp, College Station, TX, USA).

Techniques:

Primary water sources among women of mixed  HIV status  in Nyanza, Kenya, by quality of source *

Journal: Global public health

Article Title: “I know how stressful it is to lack water!” Exploring the lived experiences of household water insecurity among pregnant and postpartum women in western Kenya

doi: 10.1080/17441692.2018.1521861

Figure Lengend Snippet: Primary water sources among women of mixed HIV status in Nyanza, Kenya, by quality of source *

Article Snippet: Differences in experiences by HIV status were tabulated using chi-square, t -tests, and Fisher’s exact tests in Stata 14.0 (StataCorp, College Station, TX, USA).

Techniques: