standardised data capture template Search Results


electronic data capture system  (SmartCare Analytics)
90
SmartCare Analytics electronic data capture system
Electronic Data Capture System, supplied by SmartCare Analytics, 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/standardised+data+capture+template/electronic+data+capture+system/pmc11381648-96-13-29
Average 90 stars, based on 1 article reviews
electronic data capture system - by Bioz Stars, 2026-09
90/100 stars
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asgr1 polyclonal antibody  (Proteintech)
95
Proteintech asgr1 polyclonal antibody
Fig. 4 | Detection range and limitation. a Study design for comparative proteomic analysis across various tissue volumes using in-gel (blue) and in-tip (red) digestions. Peptides from different diameters are analyzed using data-dependent acquisition mass spectrometry (DDA-MS; n = 3 technical replicates) and data-independent acquisition mass spectrometry (DIA-MS; n = 3 technical replicates). b Number of identified peptides and proteins for varied tissue volumes using in-gel and in-tip digestions as shown in (a), including in-gel DDA-MS (light blue), in-gel DIA-MS (blue), in-tip DDA-MS (orange), and in-tip DIA-MS (red). n = 3 technical replicates for each method and tissue volume. Data were presented as mean values ± standard deviation. c <t>Asialoglycoprotein</t> <t>receptor</t> <t>1</t> <t>(ASGR1;</t> yellow) and nuclear (blue) staining image of a mouse liver formalin-fixed paraffin-embedded (FFPE) slice before gel-making (n = 1). d ASGR1 and nuclear staining image of a mouse liver FFPE slice after gel-making (n = 1). e ASGR1 and nuclear staining image of a mouse liver FFPE slice after drying onto laser capture microdissection frame slide (n = 1). Scale bars are provided. f Comparison of proteins between single nucleus (n = 5 biolo- gical replicates; blue) and single mononuclear hepatocyte (n = 6 biological
Asgr1 Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/standardised+data+capture+template/ASGR1+Antibody/pm39477916-305-33-36
Average 95 stars, based on 1 article reviews
asgr1 polyclonal antibody - by Bioz Stars, 2026-09
95/100 stars
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32-channel rf receive head coil  (Siemens AG)
90
Siemens AG 32-channel rf receive head coil
Fig. 4 | Detection range and limitation. a Study design for comparative proteomic analysis across various tissue volumes using in-gel (blue) and in-tip (red) digestions. Peptides from different diameters are analyzed using data-dependent acquisition mass spectrometry (DDA-MS; n = 3 technical replicates) and data-independent acquisition mass spectrometry (DIA-MS; n = 3 technical replicates). b Number of identified peptides and proteins for varied tissue volumes using in-gel and in-tip digestions as shown in (a), including in-gel DDA-MS (light blue), in-gel DIA-MS (blue), in-tip DDA-MS (orange), and in-tip DIA-MS (red). n = 3 technical replicates for each method and tissue volume. Data were presented as mean values ± standard deviation. c <t>Asialoglycoprotein</t> <t>receptor</t> <t>1</t> <t>(ASGR1;</t> yellow) and nuclear (blue) staining image of a mouse liver formalin-fixed paraffin-embedded (FFPE) slice before gel-making (n = 1). d ASGR1 and nuclear staining image of a mouse liver FFPE slice after gel-making (n = 1). e ASGR1 and nuclear staining image of a mouse liver FFPE slice after drying onto laser capture microdissection frame slide (n = 1). Scale bars are provided. f Comparison of proteins between single nucleus (n = 5 biolo- gical replicates; blue) and single mononuclear hepatocyte (n = 6 biological
32 Channel Rf Receive Head Coil, supplied by Siemens AG, 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/standardised+data+capture+template/32+channel+head+coil/pmc11474882-59-17-16
Average 90 stars, based on 1 article reviews
32-channel rf receive head coil - by Bioz Stars, 2026-09
90/100 stars
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standard 3d-t1wi-based template  (Johns Hopkins HealthCare)
90
Johns Hopkins HealthCare standard 3d-t1wi-based template
Fig. 4 | Detection range and limitation. a Study design for comparative proteomic analysis across various tissue volumes using in-gel (blue) and in-tip (red) digestions. Peptides from different diameters are analyzed using data-dependent acquisition mass spectrometry (DDA-MS; n = 3 technical replicates) and data-independent acquisition mass spectrometry (DIA-MS; n = 3 technical replicates). b Number of identified peptides and proteins for varied tissue volumes using in-gel and in-tip digestions as shown in (a), including in-gel DDA-MS (light blue), in-gel DIA-MS (blue), in-tip DDA-MS (orange), and in-tip DIA-MS (red). n = 3 technical replicates for each method and tissue volume. Data were presented as mean values ± standard deviation. c <t>Asialoglycoprotein</t> <t>receptor</t> <t>1</t> <t>(ASGR1;</t> yellow) and nuclear (blue) staining image of a mouse liver formalin-fixed paraffin-embedded (FFPE) slice before gel-making (n = 1). d ASGR1 and nuclear staining image of a mouse liver FFPE slice after gel-making (n = 1). e ASGR1 and nuclear staining image of a mouse liver FFPE slice after drying onto laser capture microdissection frame slide (n = 1). Scale bars are provided. f Comparison of proteins between single nucleus (n = 5 biolo- gical replicates; blue) and single mononuclear hepatocyte (n = 6 biological
Standard 3d T1wi Based Template, supplied by Johns Hopkins HealthCare, 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/standardised+data+capture+template/standard+3d+t1wi+based+template/pmc07268688-124-17-19
Average 90 stars, based on 1 article reviews
standard 3d-t1wi-based template - by Bioz Stars, 2026-09
90/100 stars
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jhu-mni-ss  (Johns Hopkins HealthCare)
90
Johns Hopkins HealthCare jhu-mni-ss
Fig. 4 | Detection range and limitation. a Study design for comparative proteomic analysis across various tissue volumes using in-gel (blue) and in-tip (red) digestions. Peptides from different diameters are analyzed using data-dependent acquisition mass spectrometry (DDA-MS; n = 3 technical replicates) and data-independent acquisition mass spectrometry (DIA-MS; n = 3 technical replicates). b Number of identified peptides and proteins for varied tissue volumes using in-gel and in-tip digestions as shown in (a), including in-gel DDA-MS (light blue), in-gel DIA-MS (blue), in-tip DDA-MS (orange), and in-tip DIA-MS (red). n = 3 technical replicates for each method and tissue volume. Data were presented as mean values ± standard deviation. c <t>Asialoglycoprotein</t> <t>receptor</t> <t>1</t> <t>(ASGR1;</t> yellow) and nuclear (blue) staining image of a mouse liver formalin-fixed paraffin-embedded (FFPE) slice before gel-making (n = 1). d ASGR1 and nuclear staining image of a mouse liver FFPE slice after gel-making (n = 1). e ASGR1 and nuclear staining image of a mouse liver FFPE slice after drying onto laser capture microdissection frame slide (n = 1). Scale bars are provided. f Comparison of proteins between single nucleus (n = 5 biolo- gical replicates; blue) and single mononuclear hepatocyte (n = 6 biological
Jhu Mni Ss, supplied by Johns Hopkins HealthCare, 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/standardised+data+capture+template/jhu+mni+ss/pmc07963761-91-15-16
Average 90 stars, based on 1 article reviews
jhu-mni-ss - by Bioz Stars, 2026-09
90/100 stars
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six cameras motion capture system  (Oxford Metrics)
86
Oxford Metrics six cameras motion capture system
Fig. 4 | Detection range and limitation. a Study design for comparative proteomic analysis across various tissue volumes using in-gel (blue) and in-tip (red) digestions. Peptides from different diameters are analyzed using data-dependent acquisition mass spectrometry (DDA-MS; n = 3 technical replicates) and data-independent acquisition mass spectrometry (DIA-MS; n = 3 technical replicates). b Number of identified peptides and proteins for varied tissue volumes using in-gel and in-tip digestions as shown in (a), including in-gel DDA-MS (light blue), in-gel DIA-MS (blue), in-tip DDA-MS (orange), and in-tip DIA-MS (red). n = 3 technical replicates for each method and tissue volume. Data were presented as mean values ± standard deviation. c <t>Asialoglycoprotein</t> <t>receptor</t> <t>1</t> <t>(ASGR1;</t> yellow) and nuclear (blue) staining image of a mouse liver formalin-fixed paraffin-embedded (FFPE) slice before gel-making (n = 1). d ASGR1 and nuclear staining image of a mouse liver FFPE slice after gel-making (n = 1). e ASGR1 and nuclear staining image of a mouse liver FFPE slice after drying onto laser capture microdissection frame slide (n = 1). Scale bars are provided. f Comparison of proteins between single nucleus (n = 5 biolo- gical replicates; blue) and single mononuclear hepatocyte (n = 6 biological
Six Cameras Motion Capture System, supplied by Oxford Metrics, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/standardised+data+capture+template/10+camera+capture+motion+system/pmc13032992-101-42-48
Average 86 stars, based on 1 article reviews
six cameras motion capture system - by Bioz Stars, 2026-09
86/100 stars
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trigno wireless emg sensors  (Delsys Inc)
98
Delsys Inc trigno wireless emg sensors
Fig. 4 | Detection range and limitation. a Study design for comparative proteomic analysis across various tissue volumes using in-gel (blue) and in-tip (red) digestions. Peptides from different diameters are analyzed using data-dependent acquisition mass spectrometry (DDA-MS; n = 3 technical replicates) and data-independent acquisition mass spectrometry (DIA-MS; n = 3 technical replicates). b Number of identified peptides and proteins for varied tissue volumes using in-gel and in-tip digestions as shown in (a), including in-gel DDA-MS (light blue), in-gel DIA-MS (blue), in-tip DDA-MS (orange), and in-tip DIA-MS (red). n = 3 technical replicates for each method and tissue volume. Data were presented as mean values ± standard deviation. c <t>Asialoglycoprotein</t> <t>receptor</t> <t>1</t> <t>(ASGR1;</t> yellow) and nuclear (blue) staining image of a mouse liver formalin-fixed paraffin-embedded (FFPE) slice before gel-making (n = 1). d ASGR1 and nuclear staining image of a mouse liver FFPE slice after gel-making (n = 1). e ASGR1 and nuclear staining image of a mouse liver FFPE slice after drying onto laser capture microdissection frame slide (n = 1). Scale bars are provided. f Comparison of proteins between single nucleus (n = 5 biolo- gical replicates; blue) and single mononuclear hepatocyte (n = 6 biological
Trigno Wireless Emg Sensors, supplied by Delsys Inc, 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/standardised+data+capture+template/Trigno+Standard/10__1109_slash_tnsre__2023__3290293-147-10-9
Average 98 stars, based on 1 article reviews
trigno wireless emg sensors - by Bioz Stars, 2026-09
98/100 stars
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computer-assisted telephone interview software  (Voxco Inc)
90
Voxco Inc computer-assisted telephone interview software
Fig. 4 | Detection range and limitation. a Study design for comparative proteomic analysis across various tissue volumes using in-gel (blue) and in-tip (red) digestions. Peptides from different diameters are analyzed using data-dependent acquisition mass spectrometry (DDA-MS; n = 3 technical replicates) and data-independent acquisition mass spectrometry (DIA-MS; n = 3 technical replicates). b Number of identified peptides and proteins for varied tissue volumes using in-gel and in-tip digestions as shown in (a), including in-gel DDA-MS (light blue), in-gel DIA-MS (blue), in-tip DDA-MS (orange), and in-tip DIA-MS (red). n = 3 technical replicates for each method and tissue volume. Data were presented as mean values ± standard deviation. c <t>Asialoglycoprotein</t> <t>receptor</t> <t>1</t> <t>(ASGR1;</t> yellow) and nuclear (blue) staining image of a mouse liver formalin-fixed paraffin-embedded (FFPE) slice before gel-making (n = 1). d ASGR1 and nuclear staining image of a mouse liver FFPE slice after gel-making (n = 1). e ASGR1 and nuclear staining image of a mouse liver FFPE slice after drying onto laser capture microdissection frame slide (n = 1). Scale bars are provided. f Comparison of proteins between single nucleus (n = 5 biolo- gical replicates; blue) and single mononuclear hepatocyte (n = 6 biological
Computer Assisted Telephone Interview Software, supplied by Voxco Inc, 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/standardised+data+capture+template/computer+assisted+telephone+interview+software/pmc06848721-155-12-16
Average 90 stars, based on 1 article reviews
computer-assisted telephone interview software - by Bioz Stars, 2026-09
90/100 stars
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oxford-astrazeneca  (AstraZeneca ltd)
90
AstraZeneca ltd oxford-astrazeneca
Fig. 4 | Detection range and limitation. a Study design for comparative proteomic analysis across various tissue volumes using in-gel (blue) and in-tip (red) digestions. Peptides from different diameters are analyzed using data-dependent acquisition mass spectrometry (DDA-MS; n = 3 technical replicates) and data-independent acquisition mass spectrometry (DIA-MS; n = 3 technical replicates). b Number of identified peptides and proteins for varied tissue volumes using in-gel and in-tip digestions as shown in (a), including in-gel DDA-MS (light blue), in-gel DIA-MS (blue), in-tip DDA-MS (orange), and in-tip DIA-MS (red). n = 3 technical replicates for each method and tissue volume. Data were presented as mean values ± standard deviation. c <t>Asialoglycoprotein</t> <t>receptor</t> <t>1</t> <t>(ASGR1;</t> yellow) and nuclear (blue) staining image of a mouse liver formalin-fixed paraffin-embedded (FFPE) slice before gel-making (n = 1). d ASGR1 and nuclear staining image of a mouse liver FFPE slice after gel-making (n = 1). e ASGR1 and nuclear staining image of a mouse liver FFPE slice after drying onto laser capture microdissection frame slide (n = 1). Scale bars are provided. f Comparison of proteins between single nucleus (n = 5 biolo- gical replicates; blue) and single mononuclear hepatocyte (n = 6 biological
Oxford Astrazeneca, supplied by AstraZeneca ltd, 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/standardised+data+capture+template/chadox1+ncov+19/pmc11115231-92-5-13
Average 90 stars, based on 1 article reviews
oxford-astrazeneca - by Bioz Stars, 2026-09
90/100 stars
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gold standard vicon system  (Oxford Metrics)
86
Oxford Metrics gold standard vicon system
Fig. 4 | Detection range and limitation. a Study design for comparative proteomic analysis across various tissue volumes using in-gel (blue) and in-tip (red) digestions. Peptides from different diameters are analyzed using data-dependent acquisition mass spectrometry (DDA-MS; n = 3 technical replicates) and data-independent acquisition mass spectrometry (DIA-MS; n = 3 technical replicates). b Number of identified peptides and proteins for varied tissue volumes using in-gel and in-tip digestions as shown in (a), including in-gel DDA-MS (light blue), in-gel DIA-MS (blue), in-tip DDA-MS (orange), and in-tip DIA-MS (red). n = 3 technical replicates for each method and tissue volume. Data were presented as mean values ± standard deviation. c <t>Asialoglycoprotein</t> <t>receptor</t> <t>1</t> <t>(ASGR1;</t> yellow) and nuclear (blue) staining image of a mouse liver formalin-fixed paraffin-embedded (FFPE) slice before gel-making (n = 1). d ASGR1 and nuclear staining image of a mouse liver FFPE slice after gel-making (n = 1). e ASGR1 and nuclear staining image of a mouse liver FFPE slice after drying onto laser capture microdissection frame slide (n = 1). Scale bars are provided. f Comparison of proteins between single nucleus (n = 5 biolo- gical replicates; blue) and single mononuclear hepatocyte (n = 6 biological
Gold Standard Vicon System, supplied by Oxford Metrics, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/standardised+data+capture+template/gold+standard/nichols_julia_kathryn__2016__the_development_of_a_low_cost_motion_capture_system_for_quantitative_clinical_assessments-943-6-8
Average 86 stars, based on 1 article reviews
gold standard vicon system - by Bioz Stars, 2026-09
86/100 stars
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clinical trial software for electronic data capture  (OpenClinica LLC)
90
OpenClinica LLC clinical trial software for electronic data capture
Fig. 4 | Detection range and limitation. a Study design for comparative proteomic analysis across various tissue volumes using in-gel (blue) and in-tip (red) digestions. Peptides from different diameters are analyzed using data-dependent acquisition mass spectrometry (DDA-MS; n = 3 technical replicates) and data-independent acquisition mass spectrometry (DIA-MS; n = 3 technical replicates). b Number of identified peptides and proteins for varied tissue volumes using in-gel and in-tip digestions as shown in (a), including in-gel DDA-MS (light blue), in-gel DIA-MS (blue), in-tip DDA-MS (orange), and in-tip DIA-MS (red). n = 3 technical replicates for each method and tissue volume. Data were presented as mean values ± standard deviation. c <t>Asialoglycoprotein</t> <t>receptor</t> <t>1</t> <t>(ASGR1;</t> yellow) and nuclear (blue) staining image of a mouse liver formalin-fixed paraffin-embedded (FFPE) slice before gel-making (n = 1). d ASGR1 and nuclear staining image of a mouse liver FFPE slice after gel-making (n = 1). e ASGR1 and nuclear staining image of a mouse liver FFPE slice after drying onto laser capture microdissection frame slide (n = 1). Scale bars are provided. f Comparison of proteins between single nucleus (n = 5 biolo- gical replicates; blue) and single mononuclear hepatocyte (n = 6 biological
Clinical Trial Software For Electronic Data Capture, supplied by OpenClinica LLC, 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/standardised+data+capture+template/electronic+data+capture+system/pmc07082032__pone__0230382__s003-257-15-17
Average 90 stars, based on 1 article reviews
clinical trial software for electronic data capture - by Bioz Stars, 2026-09
90/100 stars
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data entry software stata  (STATA Corporation)
99
STATA Corporation data entry software stata
Fig. 4 | Detection range and limitation. a Study design for comparative proteomic analysis across various tissue volumes using in-gel (blue) and in-tip (red) digestions. Peptides from different diameters are analyzed using data-dependent acquisition mass spectrometry (DDA-MS; n = 3 technical replicates) and data-independent acquisition mass spectrometry (DIA-MS; n = 3 technical replicates). b Number of identified peptides and proteins for varied tissue volumes using in-gel and in-tip digestions as shown in (a), including in-gel DDA-MS (light blue), in-gel DIA-MS (blue), in-tip DDA-MS (orange), and in-tip DIA-MS (red). n = 3 technical replicates for each method and tissue volume. Data were presented as mean values ± standard deviation. c <t>Asialoglycoprotein</t> <t>receptor</t> <t>1</t> <t>(ASGR1;</t> yellow) and nuclear (blue) staining image of a mouse liver formalin-fixed paraffin-embedded (FFPE) slice before gel-making (n = 1). d ASGR1 and nuclear staining image of a mouse liver FFPE slice after gel-making (n = 1). e ASGR1 and nuclear staining image of a mouse liver FFPE slice after drying onto laser capture microdissection frame slide (n = 1). Scale bars are provided. f Comparison of proteins between single nucleus (n = 5 biolo- gical replicates; blue) and single mononuclear hepatocyte (n = 6 biological
Data Entry Software Stata, 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
https://www.bioz.com/product/standardised+data+capture+template/STATA+1%2E0/pmc04437745-158-8-11
Average 99 stars, based on 1 article reviews
data entry software stata - by Bioz Stars, 2026-09
99/100 stars
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Image Search Results


Fig. 4 | Detection range and limitation. a Study design for comparative proteomic analysis across various tissue volumes using in-gel (blue) and in-tip (red) digestions. Peptides from different diameters are analyzed using data-dependent acquisition mass spectrometry (DDA-MS; n = 3 technical replicates) and data-independent acquisition mass spectrometry (DIA-MS; n = 3 technical replicates). b Number of identified peptides and proteins for varied tissue volumes using in-gel and in-tip digestions as shown in (a), including in-gel DDA-MS (light blue), in-gel DIA-MS (blue), in-tip DDA-MS (orange), and in-tip DIA-MS (red). n = 3 technical replicates for each method and tissue volume. Data were presented as mean values ± standard deviation. c Asialoglycoprotein receptor 1 (ASGR1; yellow) and nuclear (blue) staining image of a mouse liver formalin-fixed paraffin-embedded (FFPE) slice before gel-making (n = 1). d ASGR1 and nuclear staining image of a mouse liver FFPE slice after gel-making (n = 1). e ASGR1 and nuclear staining image of a mouse liver FFPE slice after drying onto laser capture microdissection frame slide (n = 1). Scale bars are provided. f Comparison of proteins between single nucleus (n = 5 biolo- gical replicates; blue) and single mononuclear hepatocyte (n = 6 biological

Journal: Nature communications

Article Title: Spatial proteomics of single cells and organelles on tissue slides using filter-aided expansion proteomics.

doi: 10.1038/s41467-024-53683-7

Figure Lengend Snippet: Fig. 4 | Detection range and limitation. a Study design for comparative proteomic analysis across various tissue volumes using in-gel (blue) and in-tip (red) digestions. Peptides from different diameters are analyzed using data-dependent acquisition mass spectrometry (DDA-MS; n = 3 technical replicates) and data-independent acquisition mass spectrometry (DIA-MS; n = 3 technical replicates). b Number of identified peptides and proteins for varied tissue volumes using in-gel and in-tip digestions as shown in (a), including in-gel DDA-MS (light blue), in-gel DIA-MS (blue), in-tip DDA-MS (orange), and in-tip DIA-MS (red). n = 3 technical replicates for each method and tissue volume. Data were presented as mean values ± standard deviation. c Asialoglycoprotein receptor 1 (ASGR1; yellow) and nuclear (blue) staining image of a mouse liver formalin-fixed paraffin-embedded (FFPE) slice before gel-making (n = 1). d ASGR1 and nuclear staining image of a mouse liver FFPE slice after gel-making (n = 1). e ASGR1 and nuclear staining image of a mouse liver FFPE slice after drying onto laser capture microdissection frame slide (n = 1). Scale bars are provided. f Comparison of proteins between single nucleus (n = 5 biolo- gical replicates; blue) and single mononuclear hepatocyte (n = 6 biological

Article Snippet: The tissue section was incubated for 30min in citrate antigen retrieval solution (Leagene, China) and subsequently in blocking buffer (Sangon, China) at room temperature for 1 h. The section was then incubated with ASGR1 polyclonal antibody (Proteintech, China) at a 1:200 dilution.

Techniques: Data-dependent acquisition, Mass Spectrometry, Data-independent acquisition, Standard Deviation, Staining, Laser Capture Microdissection, Comparison