celltrace dye celltracetm violet cell proliferation kit Search Results


fluorescein isothiocyanate fitc carboxyfluorescein succinimidyl ester  (Thermo Fisher)
99
Thermo Fisher fluorescein isothiocyanate fitc carboxyfluorescein succinimidyl ester
Fluorescein Isothiocyanate Fitc Carboxyfluorescein Succinimidyl Ester, supplied by Thermo Fisher, 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/celltrace+dye+celltracetm+violet+cell+proliferation+kit/pmc09606771-85-0-12?v=Thermo+Fisher
Average 99 stars, based on 1 article reviews
fluorescein isothiocyanate fitc carboxyfluorescein succinimidyl ester - by Bioz Stars, 2026-07
99/100 stars
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celltracetm cfse  (Thermo Fisher)
97
Thermo Fisher celltracetm cfse
MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the <t>CFSE</t> fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. B. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. C. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response.
Celltracetm Cfse, supplied by Thermo Fisher, 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/celltrace+dye+celltracetm+violet+cell+proliferation+kit/pmc10838760-113-11-19?v=Thermo+Fisher
Average 97 stars, based on 1 article reviews
celltracetm cfse - by Bioz Stars, 2026-07
97/100 stars
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celltracetm cell proliferation kits  (Introgen Inc)
90
Introgen Inc celltracetm cell proliferation kits
MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the <t>CFSE</t> fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. B. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. C. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response.
Celltracetm Cell Proliferation Kits, supplied by Introgen 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/celltrace+dye+celltracetm+violet+cell+proliferation+kit/pm37907476-261-1-5?v=Introgen+Inc
Average 90 stars, based on 1 article reviews
celltracetm cell proliferation kits - by Bioz Stars, 2026-07
90/100 stars
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cfse  (Thermo Fisher)
99
Thermo Fisher cfse
MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the <t>CFSE</t> fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. B. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. C. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response.
Cfse, supplied by Thermo Fisher, 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/celltrace+dye+celltracetm+violet+cell+proliferation+kit/pmc06287801-262-8-26?v=Thermo+Fisher
Average 99 stars, based on 1 article reviews
cfse - by Bioz Stars, 2026-07
99/100 stars
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celltracetm far red cell proliferation kit  (Thermo Fisher)
99
Thermo Fisher celltracetm far red cell proliferation kit
MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the <t>CFSE</t> fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. B. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. C. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response.
Celltracetm Far Red Cell Proliferation Kit, supplied by Thermo Fisher, 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/celltrace+dye+celltracetm+violet+cell+proliferation+kit/pmc10618420-51-6-12?v=Thermo+Fisher
Average 99 stars, based on 1 article reviews
celltracetm far red cell proliferation kit - by Bioz Stars, 2026-07
99/100 stars
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celltracetm violet dye  (STEMCELL Technologies Inc)
90
STEMCELL Technologies Inc celltracetm violet dye
MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the <t>CFSE</t> fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. B. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. C. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response.
Celltracetm Violet Dye, supplied by STEMCELL Technologies 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/celltrace+dye+celltracetm+violet+cell+proliferation+kit/pmc09493073__Presentation_1-17-14-10?v=STEMCELL+Technologies+Inc
Average 90 stars, based on 1 article reviews
celltracetm violet dye - by Bioz Stars, 2026-07
90/100 stars
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celltracktm autoprep analyzer  (CellSearch inc)
90
CellSearch inc celltracktm autoprep analyzer
MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the <t>CFSE</t> fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. B. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. C. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response.
Celltracktm Autoprep Analyzer, supplied by CellSearch 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/celltrace+dye+celltracetm+violet+cell+proliferation+kit/pm19115104-45-32-35?v=CellSearch+inc
Average 90 stars, based on 1 article reviews
celltracktm autoprep analyzer - by Bioz Stars, 2026-07
90/100 stars
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celltracetm far red cell proliferation kit s2  (Thermo Fisher)
99
Thermo Fisher celltracetm far red cell proliferation kit s2
MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the <t>CFSE</t> fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. B. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. C. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response.
Celltracetm Far Red Cell Proliferation Kit S2, supplied by Thermo Fisher, 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/celltrace+dye+celltracetm+violet+cell+proliferation+kit/pm32216337__ja0c00221_si_001-21-0-24?v=Thermo+Fisher
Average 99 stars, based on 1 article reviews
celltracetm far red cell proliferation kit s2 - by Bioz Stars, 2026-07
99/100 stars
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celltracetm mouse cd8 enrichment kit  (STEMCELL Technologies Inc)
90
STEMCELL Technologies Inc celltracetm mouse cd8 enrichment kit
MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the <t>CFSE</t> fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. B. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. C. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response.
Celltracetm Mouse Cd8 Enrichment Kit, supplied by STEMCELL Technologies 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/celltrace+dye+celltracetm+violet+cell+proliferation+kit/10__1080_slash_2162402x__2025__2497171-89-12-17?v=STEMCELL+Technologies+Inc
Average 90 stars, based on 1 article reviews
celltracetm mouse cd8 enrichment kit - by Bioz Stars, 2026-07
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celltracetm cfse cell proliferation kit invitrogen c34554 zombie nirtm fixable viability kit biolegend  (Thermo Fisher)
96
Thermo Fisher celltracetm cfse cell proliferation kit invitrogen c34554 zombie nirtm fixable viability kit biolegend
MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the <t>CFSE</t> fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. B. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. C. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response.
Celltracetm Cfse Cell Proliferation Kit Invitrogen C34554 Zombie Nirtm Fixable Viability Kit Biolegend, supplied by Thermo Fisher, 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/celltrace+dye+celltracetm+violet+cell+proliferation+kit/pm39789356-393-96-101?v=Thermo+Fisher
Average 96 stars, based on 1 article reviews
celltracetm cfse cell proliferation kit invitrogen c34554 zombie nirtm fixable viability kit biolegend - by Bioz Stars, 2026-07
96/100 stars
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celltracetm violet cell proliferation kit  (Thermo Fisher)
99
Thermo Fisher celltracetm violet cell proliferation kit
MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the <t>CFSE</t> fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. B. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. C. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response.
Celltracetm Violet Cell Proliferation Kit, supplied by Thermo Fisher, 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/celltrace+dye+celltracetm+violet+cell+proliferation+kit/pm33609620-80-0-18?v=Thermo+Fisher
Average 99 stars, based on 1 article reviews
celltracetm violet cell proliferation kit - by Bioz Stars, 2026-07
99/100 stars
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celltiter glo® luminescent cell viability assay  (Promega)
90
Promega celltiter glo® luminescent cell viability assay
MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the <t>CFSE</t> fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. B. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. C. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response.
Celltiter Glo® Luminescent Cell Viability Assay, supplied by Promega, 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/celltrace+dye+celltracetm+violet+cell+proliferation+kit/us10663457-477-20-77?v=Promega
Average 90 stars, based on 1 article reviews
celltiter glo® luminescent cell viability assay - by Bioz Stars, 2026-07
90/100 stars
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Image Search Results


MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. B. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. C. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response.

Journal: Heliyon

Article Title: The immunogenic profile and immunomodulatory function of mesenchymal stromal / stem cells in the presence of Ptychotis verticillata

doi: 10.1016/j.heliyon.2024.e24822

Figure Lengend Snippet: MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. B. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response. C. MSCs do not induce PBMC allogeneic response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic PBMC were incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of PBMC was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the % of the allogeneic PBMC response.

Article Snippet: The proliferation of PBMCs and T cells was assessed using the CellTraceTM CFSE (carboxyfluorescein succinimidyl ester) Cell proliferation kit (Invitrogen, Molecular Probes, USA).

Techniques: Incubation, Cell Culture, Flow Cytometry, Fluorescence

Pretreated MSCs differentially modulate activated T-cell response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic T-cells were activated and incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of activated lymphocytes was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the percentage of stimulated T-cell response. B. Pretreated MSCs differentially modulate activated T-cell response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic T-cells were activated and incubated in the presence or absence of MSCs and cultured without direct contact for 05 days. The proliferation of activated lymphocytes was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the percentage of stimulated T-cell response.

Journal: Heliyon

Article Title: The immunogenic profile and immunomodulatory function of mesenchymal stromal / stem cells in the presence of Ptychotis verticillata

doi: 10.1016/j.heliyon.2024.e24822

Figure Lengend Snippet: Pretreated MSCs differentially modulate activated T-cell response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic T-cells were activated and incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of activated lymphocytes was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the percentage of stimulated T-cell response. B. Pretreated MSCs differentially modulate activated T-cell response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Essential Oil (HE) for 24h (a), 72h (b), and 5 days (c). Allogeneic T-cells were activated and incubated in the presence or absence of MSCs and cultured without direct contact for 05 days. The proliferation of activated lymphocytes was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the percentage of stimulated T-cell response.

Article Snippet: The proliferation of PBMCs and T cells was assessed using the CellTraceTM CFSE (carboxyfluorescein succinimidyl ester) Cell proliferation kit (Invitrogen, Molecular Probes, USA).

Techniques: Incubation, Cell Culture, Flow Cytometry, Fluorescence

Pretreated MSCs differentially modulate activated T-cell response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic T-cells were activated and incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of activated lymphocytes was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the percentage of stimulated T-cell response. B. Pretreated MSCs differentially modulate activated T-cell response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic T-cells were activated and incubated in the presence or absence of MSCs and cultured without direct contact for 05 days. The proliferation of activated lymphocytes was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the percentage of stimulated T-cell response.

Journal: Heliyon

Article Title: The immunogenic profile and immunomodulatory function of mesenchymal stromal / stem cells in the presence of Ptychotis verticillata

doi: 10.1016/j.heliyon.2024.e24822

Figure Lengend Snippet: Pretreated MSCs differentially modulate activated T-cell response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic T-cells were activated and incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of activated lymphocytes was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the percentage of stimulated T-cell response. B. Pretreated MSCs differentially modulate activated T-cell response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Thymol (THY) for 24h (a), 72h (b), and 5 days (c). Allogeneic T-cells were activated and incubated in the presence or absence of MSCs and cultured without direct contact for 05 days. The proliferation of activated lymphocytes was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the percentage of stimulated T-cell response.

Article Snippet: The proliferation of PBMCs and T cells was assessed using the CellTraceTM CFSE (carboxyfluorescein succinimidyl ester) Cell proliferation kit (Invitrogen, Molecular Probes, USA).

Techniques: Incubation, Cell Culture, Flow Cytometry, Fluorescence

Pretreated MSCs differentially modulate activated T-cell response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic T-cells were activated and incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of activated lymphocytes was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the percentage of stimulated T-cell response. B. Pretreated MSCs differentially modulate activated T-cell response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic T-cells were activated and incubated in the presence or absence of MSCs and cultured without direct contact for 05 days. The proliferation of activated lymphocytes was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the percentage of stimulated T-cell response.

Journal: Heliyon

Article Title: The immunogenic profile and immunomodulatory function of mesenchymal stromal / stem cells in the presence of Ptychotis verticillata

doi: 10.1016/j.heliyon.2024.e24822

Figure Lengend Snippet: Pretreated MSCs differentially modulate activated T-cell response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic T-cells were activated and incubated in the presence or absence of MSCs and cultured with direct contact for 05 days. The proliferation of activated lymphocytes was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the percentage of stimulated T-cell response. B. Pretreated MSCs differentially modulate activated T-cell response. MSCs were or were not pretreated at different times with various concentrations of PV compounds Carvacrol (CR) for 24h (a), 72h (b), and 5 days (c). Allogeneic T-cells were activated and incubated in the presence or absence of MSCs and cultured without direct contact for 05 days. The proliferation of activated lymphocytes was assessed by flow cytometry measurement of the CFSE fluorescence. The data are expressed as the mean ± SEM of the percentage of stimulated T-cell response.

Article Snippet: The proliferation of PBMCs and T cells was assessed using the CellTraceTM CFSE (carboxyfluorescein succinimidyl ester) Cell proliferation kit (Invitrogen, Molecular Probes, USA).

Techniques: Incubation, Cell Culture, Flow Cytometry, Fluorescence