statistical software version 10 0 Search Results


99
STATA Corporation stata 10
Stata 10, 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/statistical+software+version+10+0/pm21279993-92-4-4?v=STATA+Corporation
Average 99 stars, based on 1 article reviews
stata 10 - by Bioz Stars, 2026-07
99/100 stars
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90
GraphPad Software Inc version 10.0.0 for windows
Version 10.0.0 For Windows, supplied by GraphPad 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
https://www.bioz.com/product/statistical+software+version+10+0/pmc11879608-134-0-5?v=GraphPad+Software+Inc
Average 90 stars, based on 1 article reviews
version 10.0.0 for windows - by Bioz Stars, 2026-07
90/100 stars
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90
Esri inc arcgis software arcgis locator version 10.0
Arcgis Software Arcgis Locator Version 10.0, supplied by Esri 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/statistical+software+version+10+0/pmc07525465-123-21-27?v=Esri+inc
Average 90 stars, based on 1 article reviews
arcgis software arcgis locator version 10.0 - by Bioz Stars, 2026-07
90/100 stars
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90
Dynamic Microsystems Inc statistical software program gb-stat version 10.0
Statistical Software Program Gb Stat Version 10.0, supplied by Dynamic Microsystems 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/statistical+software+version+10+0/pmc05837602-101-39-45?v=Dynamic+Microsystems+Inc
Average 90 stars, based on 1 article reviews
statistical software program gb-stat version 10.0 - by Bioz Stars, 2026-07
90/100 stars
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90
GraphPad Software Inc spss 10.0 software package
Spss 10.0 Software Package, supplied by GraphPad 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
https://www.bioz.com/product/statistical+software+version+10+0/pmc03276698-137-7-10?v=GraphPad+Software+Inc
Average 90 stars, based on 1 article reviews
spss 10.0 software package - by Bioz Stars, 2026-07
90/100 stars
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90
Becton Dickinson software version 10.0
Gating Strategy. We first gated total leukocytes on a time/side scatter density plot and selected the Zombie UV negative cell population for detecting living cells. Next, we gated living cells for singlets on a forward scatter/trigger pulse width density plot. After recognizing cells by size and granularity, we selected monocytes on the HLA-DR gate. Then, we gated monocytes using the rectangular gating strategy on the CD14 + /CD16 + cell population to identify CD14 ++ CD16 − cells as classical monocytes, CD14 ++ CD16 + cells as intermediate monocytes, and CD14 + CD16 + cells as nonclassical monocytes . We obtained the median fluorescence intensity (MFI) for CCR2 by considering both positive and negative cell populations. We got the CCR2 + cell percentage using fluorescence minus one (FMO) control. For each fluorochrome, we used compensation controls through UltraComp eBeads TM (Invitrogen TM , Carlsbad, CA, USA). We analyzed data by the <t>FlowJo</t> 10.0.7 software (TreeStar, Inc., Ashland, OR, USA).
Software Version 10.0, supplied by Becton Dickinson, 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/statistical+software+version+10+0/pmc09604509-113-6-6?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
software version 10.0 - by Bioz Stars, 2026-07
90/100 stars
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90
MedCalc Software Ltd statistical software version 10.0.2.0
Gating Strategy. We first gated total leukocytes on a time/side scatter density plot and selected the Zombie UV negative cell population for detecting living cells. Next, we gated living cells for singlets on a forward scatter/trigger pulse width density plot. After recognizing cells by size and granularity, we selected monocytes on the HLA-DR gate. Then, we gated monocytes using the rectangular gating strategy on the CD14 + /CD16 + cell population to identify CD14 ++ CD16 − cells as classical monocytes, CD14 ++ CD16 + cells as intermediate monocytes, and CD14 + CD16 + cells as nonclassical monocytes . We obtained the median fluorescence intensity (MFI) for CCR2 by considering both positive and negative cell populations. We got the CCR2 + cell percentage using fluorescence minus one (FMO) control. For each fluorochrome, we used compensation controls through UltraComp eBeads TM (Invitrogen TM , Carlsbad, CA, USA). We analyzed data by the <t>FlowJo</t> 10.0.7 software (TreeStar, Inc., Ashland, OR, USA).
Statistical Software Version 10.0.2.0, supplied by MedCalc Software 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/statistical+software+version+10+0/pmc08882571-54-9-9?v=MedCalc+Software+Ltd
Average 90 stars, based on 1 article reviews
statistical software version 10.0.2.0 - by Bioz Stars, 2026-07
90/100 stars
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90
SAS institute version 10.0 software
Gating Strategy. We first gated total leukocytes on a time/side scatter density plot and selected the Zombie UV negative cell population for detecting living cells. Next, we gated living cells for singlets on a forward scatter/trigger pulse width density plot. After recognizing cells by size and granularity, we selected monocytes on the HLA-DR gate. Then, we gated monocytes using the rectangular gating strategy on the CD14 + /CD16 + cell population to identify CD14 ++ CD16 − cells as classical monocytes, CD14 ++ CD16 + cells as intermediate monocytes, and CD14 + CD16 + cells as nonclassical monocytes . We obtained the median fluorescence intensity (MFI) for CCR2 by considering both positive and negative cell populations. We got the CCR2 + cell percentage using fluorescence minus one (FMO) control. For each fluorochrome, we used compensation controls through UltraComp eBeads TM (Invitrogen TM , Carlsbad, CA, USA). We analyzed data by the <t>FlowJo</t> 10.0.7 software (TreeStar, Inc., Ashland, OR, USA).
Version 10.0 Software, supplied by SAS institute, 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/statistical+software+version+10+0/pmc06266265-349-10-13?v=SAS+institute
Average 90 stars, based on 1 article reviews
version 10.0 software - by Bioz Stars, 2026-07
90/100 stars
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90
SPSS Inc computer software, version 10
Gating Strategy. We first gated total leukocytes on a time/side scatter density plot and selected the Zombie UV negative cell population for detecting living cells. Next, we gated living cells for singlets on a forward scatter/trigger pulse width density plot. After recognizing cells by size and granularity, we selected monocytes on the HLA-DR gate. Then, we gated monocytes using the rectangular gating strategy on the CD14 + /CD16 + cell population to identify CD14 ++ CD16 − cells as classical monocytes, CD14 ++ CD16 + cells as intermediate monocytes, and CD14 + CD16 + cells as nonclassical monocytes . We obtained the median fluorescence intensity (MFI) for CCR2 by considering both positive and negative cell populations. We got the CCR2 + cell percentage using fluorescence minus one (FMO) control. For each fluorochrome, we used compensation controls through UltraComp eBeads TM (Invitrogen TM , Carlsbad, CA, USA). We analyzed data by the <t>FlowJo</t> 10.0.7 software (TreeStar, Inc., Ashland, OR, USA).
Computer Software, Version 10, supplied by SPSS 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/statistical+software+version+10+0/pmc03317009-65-25-24?v=SPSS+Inc
Average 90 stars, based on 1 article reviews
computer software, version 10 - by Bioz Stars, 2026-07
90/100 stars
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90
TIBCO 10.0 statistical package
Gating Strategy. We first gated total leukocytes on a time/side scatter density plot and selected the Zombie UV negative cell population for detecting living cells. Next, we gated living cells for singlets on a forward scatter/trigger pulse width density plot. After recognizing cells by size and granularity, we selected monocytes on the HLA-DR gate. Then, we gated monocytes using the rectangular gating strategy on the CD14 + /CD16 + cell population to identify CD14 ++ CD16 − cells as classical monocytes, CD14 ++ CD16 + cells as intermediate monocytes, and CD14 + CD16 + cells as nonclassical monocytes . We obtained the median fluorescence intensity (MFI) for CCR2 by considering both positive and negative cell populations. We got the CCR2 + cell percentage using fluorescence minus one (FMO) control. For each fluorochrome, we used compensation controls through UltraComp eBeads TM (Invitrogen TM , Carlsbad, CA, USA). We analyzed data by the <t>FlowJo</t> 10.0.7 software (TreeStar, Inc., Ashland, OR, USA).
10.0 Statistical Package, supplied by TIBCO, 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/statistical+software+version+10+0/pm38132509-126-7-11?v=TIBCO
Average 90 stars, based on 1 article reviews
10.0 statistical package - by Bioz Stars, 2026-07
90/100 stars
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90
TIBCO data analysis software, version 12.0
Gating Strategy. We first gated total leukocytes on a time/side scatter density plot and selected the Zombie UV negative cell population for detecting living cells. Next, we gated living cells for singlets on a forward scatter/trigger pulse width density plot. After recognizing cells by size and granularity, we selected monocytes on the HLA-DR gate. Then, we gated monocytes using the rectangular gating strategy on the CD14 + /CD16 + cell population to identify CD14 ++ CD16 − cells as classical monocytes, CD14 ++ CD16 + cells as intermediate monocytes, and CD14 + CD16 + cells as nonclassical monocytes . We obtained the median fluorescence intensity (MFI) for CCR2 by considering both positive and negative cell populations. We got the CCR2 + cell percentage using fluorescence minus one (FMO) control. For each fluorochrome, we used compensation controls through UltraComp eBeads TM (Invitrogen TM , Carlsbad, CA, USA). We analyzed data by the <t>FlowJo</t> 10.0.7 software (TreeStar, Inc., Ashland, OR, USA).
Data Analysis Software, Version 12.0, supplied by TIBCO, 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/statistical+software+version+10+0/pmc05899339-125-4-10?v=TIBCO
Average 90 stars, based on 1 article reviews
data analysis software, version 12.0 - by Bioz Stars, 2026-07
90/100 stars
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90
GraphPad Software Inc stata statistical software version 10.0
Gating Strategy. We first gated total leukocytes on a time/side scatter density plot and selected the Zombie UV negative cell population for detecting living cells. Next, we gated living cells for singlets on a forward scatter/trigger pulse width density plot. After recognizing cells by size and granularity, we selected monocytes on the HLA-DR gate. Then, we gated monocytes using the rectangular gating strategy on the CD14 + /CD16 + cell population to identify CD14 ++ CD16 − cells as classical monocytes, CD14 ++ CD16 + cells as intermediate monocytes, and CD14 + CD16 + cells as nonclassical monocytes . We obtained the median fluorescence intensity (MFI) for CCR2 by considering both positive and negative cell populations. We got the CCR2 + cell percentage using fluorescence minus one (FMO) control. For each fluorochrome, we used compensation controls through UltraComp eBeads TM (Invitrogen TM , Carlsbad, CA, USA). We analyzed data by the <t>FlowJo</t> 10.0.7 software (TreeStar, Inc., Ashland, OR, USA).
Stata Statistical Software Version 10.0, supplied by GraphPad 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
https://www.bioz.com/product/statistical+software+version+10+0/pmc11355853-79-6-10?v=GraphPad+Software+Inc
Average 90 stars, based on 1 article reviews
stata statistical software version 10.0 - by Bioz Stars, 2026-07
90/100 stars
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Image Search Results


Gating Strategy. We first gated total leukocytes on a time/side scatter density plot and selected the Zombie UV negative cell population for detecting living cells. Next, we gated living cells for singlets on a forward scatter/trigger pulse width density plot. After recognizing cells by size and granularity, we selected monocytes on the HLA-DR gate. Then, we gated monocytes using the rectangular gating strategy on the CD14 + /CD16 + cell population to identify CD14 ++ CD16 − cells as classical monocytes, CD14 ++ CD16 + cells as intermediate monocytes, and CD14 + CD16 + cells as nonclassical monocytes . We obtained the median fluorescence intensity (MFI) for CCR2 by considering both positive and negative cell populations. We got the CCR2 + cell percentage using fluorescence minus one (FMO) control. For each fluorochrome, we used compensation controls through UltraComp eBeads TM (Invitrogen TM , Carlsbad, CA, USA). We analyzed data by the FlowJo 10.0.7 software (TreeStar, Inc., Ashland, OR, USA).

Journal: Journal of Cardiovascular Development and Disease

Article Title: The CCR2 + Monocyte Subsets Increase in Obese Boys but Not Girls with Abnormally High Carotid Intima-Media Thickness: A Pilot Study

doi: 10.3390/jcdd9100330

Figure Lengend Snippet: Gating Strategy. We first gated total leukocytes on a time/side scatter density plot and selected the Zombie UV negative cell population for detecting living cells. Next, we gated living cells for singlets on a forward scatter/trigger pulse width density plot. After recognizing cells by size and granularity, we selected monocytes on the HLA-DR gate. Then, we gated monocytes using the rectangular gating strategy on the CD14 + /CD16 + cell population to identify CD14 ++ CD16 − cells as classical monocytes, CD14 ++ CD16 + cells as intermediate monocytes, and CD14 + CD16 + cells as nonclassical monocytes . We obtained the median fluorescence intensity (MFI) for CCR2 by considering both positive and negative cell populations. We got the CCR2 + cell percentage using fluorescence minus one (FMO) control. For each fluorochrome, we used compensation controls through UltraComp eBeads TM (Invitrogen TM , Carlsbad, CA, USA). We analyzed data by the FlowJo 10.0.7 software (TreeStar, Inc., Ashland, OR, USA).

Article Snippet: We analyzed monocyte subpopulations using the FlowJo software version 10.0.

Techniques: Fluorescence, Software