primers designed with p3 primer design online software Search Results


p3 1000 promoter region size of each promoter is in parenthesis  (ATCC)
95
ATCC p3 1000 promoter region size of each promoter is in parenthesis
P3 1000 Promoter Region Size Of Each Promoter Is In Parenthesis, supplied by ATCC, 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/result/p3 1000 promoter region size of each promoter is in parenthesis/product/ATCC
Average 95 stars, based on 1 article reviews
p3 1000 promoter region size of each promoter is in parenthesis - by Bioz Stars, 2026-05
95/100 stars
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primers designed with p3 primer design online software  (PrimerDesign Inc)
90
PrimerDesign Inc primers designed with p3 primer design online software
Primers Designed With P3 Primer Design Online Software, supplied by PrimerDesign 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/result/primers designed with p3 primer design online software/product/PrimerDesign Inc
Average 90 stars, based on 1 article reviews
primers designed with p3 primer design online software - by Bioz Stars, 2026-05
90/100 stars
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p3 primer cell 96-well nucleofectortm kit  (Lonza)
90
Lonza p3 primer cell 96-well nucleofectortm kit
P3 Primer Cell 96 Well Nucleofectortm Kit, supplied by Lonza, 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/result/p3 primer cell 96-well nucleofectortm kit/product/Lonza
Average 90 stars, based on 1 article reviews
p3 primer cell 96-well nucleofectortm kit - by Bioz Stars, 2026-05
90/100 stars
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gene exp foxp3 mm00475156 m1  (Thermo Fisher)
95
Thermo Fisher gene exp foxp3 mm00475156 m1
Corneal grafts were transplanted onto inflamed high-risk or control (‘low-risk’) host beds, and their corneas and draining lymph nodes (dLNs) were analyzed 14 days post-transplantation. ( A , B ) Corneal grafts were harvested and digested with collagenase D. Single cell suspensions were stained for <t>Foxp3</t> and CD4, and analyzed using flow cytometry. 5 corneas per group were pooled for each analysis; data shown are representative of 3 independent experiments. ( C) Corneal grafts were harvested, mRNA was isolated, and Foxp3 expression was analyzed using real-time PCR 14 days post-transplantation. n = 5. ( D ) DLNs were harvested, each DLN was stained for Foxp3 and CD4, and analyzed separately using flow cytometry. Mean fluorescence intensity (MFI) of Foxp3 levels by Tregs of low-risk and high-risk graft recipients was assesssed. N = 5 mice/group, data shown are representative of 3 independent experiments. ( E ) Treg suppression assay showing Treg suppressive function of Tregs isolated from DLNs of high-risk vs. low-risk recipients 14 days post-transplantation. Suppression of naïve BALB/c CD4 + CD25 − conventional T cell proliferation by Tregs was assessed following exposure to C57BL/6 (donor) or C3H (third party) APCs. All data were obtained from n = 5 mice/group and representative data from three independent experiments are shown. p values are calculated using the Mann-Whitney test and error bars represent SEM.
Gene Exp Foxp3 Mm00475156 M1, 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
https://www.bioz.com/result/gene exp foxp3 mm00475156 m1/product/Thermo Fisher
Average 95 stars, based on 1 article reviews
gene exp foxp3 mm00475156 m1 - by Bioz Stars, 2026-05
95/100 stars
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pcb1-fw-p1d/pcb-760-rev-p3 primer set  (Marinus)
90
Marinus pcb1-fw-p1d/pcb-760-rev-p3 primer set
Corneal grafts were transplanted onto inflamed high-risk or control (‘low-risk’) host beds, and their corneas and draining lymph nodes (dLNs) were analyzed 14 days post-transplantation. ( A , B ) Corneal grafts were harvested and digested with collagenase D. Single cell suspensions were stained for <t>Foxp3</t> and CD4, and analyzed using flow cytometry. 5 corneas per group were pooled for each analysis; data shown are representative of 3 independent experiments. ( C) Corneal grafts were harvested, mRNA was isolated, and Foxp3 expression was analyzed using real-time PCR 14 days post-transplantation. n = 5. ( D ) DLNs were harvested, each DLN was stained for Foxp3 and CD4, and analyzed separately using flow cytometry. Mean fluorescence intensity (MFI) of Foxp3 levels by Tregs of low-risk and high-risk graft recipients was assesssed. N = 5 mice/group, data shown are representative of 3 independent experiments. ( E ) Treg suppression assay showing Treg suppressive function of Tregs isolated from DLNs of high-risk vs. low-risk recipients 14 days post-transplantation. Suppression of naïve BALB/c CD4 + CD25 − conventional T cell proliferation by Tregs was assessed following exposure to C57BL/6 (donor) or C3H (third party) APCs. All data were obtained from n = 5 mice/group and representative data from three independent experiments are shown. p values are calculated using the Mann-Whitney test and error bars represent SEM.
Pcb1 Fw P1d/Pcb 760 Rev P3 Primer Set, supplied by Marinus, 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/result/pcb1-fw-p1d/pcb-760-rev-p3 primer set/product/Marinus
Average 90 stars, based on 1 article reviews
pcb1-fw-p1d/pcb-760-rev-p3 primer set - by Bioz Stars, 2026-05
90/100 stars
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gene exp foxp3 hs01085832 m1  (Thermo Fisher)
87
Thermo Fisher gene exp foxp3 hs01085832 m1
Corneal grafts were transplanted onto inflamed high-risk or control (‘low-risk’) host beds, and their corneas and draining lymph nodes (dLNs) were analyzed 14 days post-transplantation. ( A , B ) Corneal grafts were harvested and digested with collagenase D. Single cell suspensions were stained for <t>Foxp3</t> and CD4, and analyzed using flow cytometry. 5 corneas per group were pooled for each analysis; data shown are representative of 3 independent experiments. ( C) Corneal grafts were harvested, mRNA was isolated, and Foxp3 expression was analyzed using real-time PCR 14 days post-transplantation. n = 5. ( D ) DLNs were harvested, each DLN was stained for Foxp3 and CD4, and analyzed separately using flow cytometry. Mean fluorescence intensity (MFI) of Foxp3 levels by Tregs of low-risk and high-risk graft recipients was assesssed. N = 5 mice/group, data shown are representative of 3 independent experiments. ( E ) Treg suppression assay showing Treg suppressive function of Tregs isolated from DLNs of high-risk vs. low-risk recipients 14 days post-transplantation. Suppression of naïve BALB/c CD4 + CD25 − conventional T cell proliferation by Tregs was assessed following exposure to C57BL/6 (donor) or C3H (third party) APCs. All data were obtained from n = 5 mice/group and representative data from three independent experiments are shown. p values are calculated using the Mann-Whitney test and error bars represent SEM.
Gene Exp Foxp3 Hs01085832 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 87/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gene exp foxp3 hs01085832 m1/product/Thermo Fisher
Average 87 stars, based on 1 article reviews
gene exp foxp3 hs01085832 m1 - by Bioz Stars, 2026-05
87/100 stars
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p1–p3 primer pair  (Federation of European Neuroscience Societies)
90
Federation of European Neuroscience Societies p1–p3 primer pair
Corneal grafts were transplanted onto inflamed high-risk or control (‘low-risk’) host beds, and their corneas and draining lymph nodes (dLNs) were analyzed 14 days post-transplantation. ( A , B ) Corneal grafts were harvested and digested with collagenase D. Single cell suspensions were stained for <t>Foxp3</t> and CD4, and analyzed using flow cytometry. 5 corneas per group were pooled for each analysis; data shown are representative of 3 independent experiments. ( C) Corneal grafts were harvested, mRNA was isolated, and Foxp3 expression was analyzed using real-time PCR 14 days post-transplantation. n = 5. ( D ) DLNs were harvested, each DLN was stained for Foxp3 and CD4, and analyzed separately using flow cytometry. Mean fluorescence intensity (MFI) of Foxp3 levels by Tregs of low-risk and high-risk graft recipients was assesssed. N = 5 mice/group, data shown are representative of 3 independent experiments. ( E ) Treg suppression assay showing Treg suppressive function of Tregs isolated from DLNs of high-risk vs. low-risk recipients 14 days post-transplantation. Suppression of naïve BALB/c CD4 + CD25 − conventional T cell proliferation by Tregs was assessed following exposure to C57BL/6 (donor) or C3H (third party) APCs. All data were obtained from n = 5 mice/group and representative data from three independent experiments are shown. p values are calculated using the Mann-Whitney test and error bars represent SEM.
P1–P3 Primer Pair, supplied by Federation of European Neuroscience Societies, 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/result/p1–p3 primer pair/product/Federation of European Neuroscience Societies
Average 90 stars, based on 1 article reviews
p1–p3 primer pair - by Bioz Stars, 2026-05
90/100 stars
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primer pair poty 59 fwd/dn1 p3 rev-noti  (HCPro Inc)
90
HCPro Inc primer pair poty 59 fwd/dn1 p3 rev-noti
Corneal grafts were transplanted onto inflamed high-risk or control (‘low-risk’) host beds, and their corneas and draining lymph nodes (dLNs) were analyzed 14 days post-transplantation. ( A , B ) Corneal grafts were harvested and digested with collagenase D. Single cell suspensions were stained for <t>Foxp3</t> and CD4, and analyzed using flow cytometry. 5 corneas per group were pooled for each analysis; data shown are representative of 3 independent experiments. ( C) Corneal grafts were harvested, mRNA was isolated, and Foxp3 expression was analyzed using real-time PCR 14 days post-transplantation. n = 5. ( D ) DLNs were harvested, each DLN was stained for Foxp3 and CD4, and analyzed separately using flow cytometry. Mean fluorescence intensity (MFI) of Foxp3 levels by Tregs of low-risk and high-risk graft recipients was assesssed. N = 5 mice/group, data shown are representative of 3 independent experiments. ( E ) Treg suppression assay showing Treg suppressive function of Tregs isolated from DLNs of high-risk vs. low-risk recipients 14 days post-transplantation. Suppression of naïve BALB/c CD4 + CD25 − conventional T cell proliferation by Tregs was assessed following exposure to C57BL/6 (donor) or C3H (third party) APCs. All data were obtained from n = 5 mice/group and representative data from three independent experiments are shown. p values are calculated using the Mann-Whitney test and error bars represent SEM.
Primer Pair Poty 59 Fwd/Dn1 P3 Rev Noti, supplied by HCPro 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/result/primer pair poty 59 fwd/dn1 p3 rev-noti/product/HCPro Inc
Average 90 stars, based on 1 article reviews
primer pair poty 59 fwd/dn1 p3 rev-noti - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier
gene exp foxp3 mm00475162 m1  (Thermo Fisher)
99
Thermo Fisher gene exp foxp3 mm00475162 m1
Corneal grafts were transplanted onto inflamed high-risk or control (‘low-risk’) host beds, and their corneas and draining lymph nodes (dLNs) were analyzed 14 days post-transplantation. ( A , B ) Corneal grafts were harvested and digested with collagenase D. Single cell suspensions were stained for <t>Foxp3</t> and CD4, and analyzed using flow cytometry. 5 corneas per group were pooled for each analysis; data shown are representative of 3 independent experiments. ( C) Corneal grafts were harvested, mRNA was isolated, and Foxp3 expression was analyzed using real-time PCR 14 days post-transplantation. n = 5. ( D ) DLNs were harvested, each DLN was stained for Foxp3 and CD4, and analyzed separately using flow cytometry. Mean fluorescence intensity (MFI) of Foxp3 levels by Tregs of low-risk and high-risk graft recipients was assesssed. N = 5 mice/group, data shown are representative of 3 independent experiments. ( E ) Treg suppression assay showing Treg suppressive function of Tregs isolated from DLNs of high-risk vs. low-risk recipients 14 days post-transplantation. Suppression of naïve BALB/c CD4 + CD25 − conventional T cell proliferation by Tregs was assessed following exposure to C57BL/6 (donor) or C3H (third party) APCs. All data were obtained from n = 5 mice/group and representative data from three independent experiments are shown. p values are calculated using the Mann-Whitney test and error bars represent SEM.
Gene Exp Foxp3 Mm00475162 M1, 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/result/gene exp foxp3 mm00475162 m1/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
gene exp foxp3 mm00475162 m1 - by Bioz Stars, 2026-05
99/100 stars
  Buy from Supplier
gene exp foxp3 hs01085834 m1  (Thermo Fisher)
99
Thermo Fisher gene exp foxp3 hs01085834 m1
Proportions of total Tregs, nTregs and mTregs based on different gating strategies in whole blood and isolated CD4 + T cells of control subjects and post‐ACS and NSTE‐ACS patients
Gene Exp Foxp3 Hs01085834 M1, 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/result/gene exp foxp3 hs01085834 m1/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
gene exp foxp3 hs01085834 m1 - by Bioz Stars, 2026-05
99/100 stars
  Buy from Supplier
p1 primers  (DuPont de Nemours)
90
DuPont de Nemours p1 primers
Proportions of total Tregs, nTregs and mTregs based on different gating strategies in whole blood and isolated CD4 + T cells of control subjects and post‐ACS and NSTE‐ACS patients
P1 Primers, supplied by DuPont de Nemours, 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/result/p1 primers/product/DuPont de Nemours
Average 90 stars, based on 1 article reviews
p1 primers - by Bioz Stars, 2026-05
90/100 stars
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gene exp foxp3 hs00203958 m1  (Thermo Fisher)
99
Thermo Fisher gene exp foxp3 hs00203958 m1
Proportions of total Tregs, nTregs and mTregs based on different gating strategies in whole blood and isolated CD4 + T cells of control subjects and post‐ACS and NSTE‐ACS patients
Gene Exp Foxp3 Hs00203958 M1, 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/result/gene exp foxp3 hs00203958 m1/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
gene exp foxp3 hs00203958 m1 - by Bioz Stars, 2026-05
99/100 stars
  Buy from Supplier

Image Search Results


Corneal grafts were transplanted onto inflamed high-risk or control (‘low-risk’) host beds, and their corneas and draining lymph nodes (dLNs) were analyzed 14 days post-transplantation. ( A , B ) Corneal grafts were harvested and digested with collagenase D. Single cell suspensions were stained for Foxp3 and CD4, and analyzed using flow cytometry. 5 corneas per group were pooled for each analysis; data shown are representative of 3 independent experiments. ( C) Corneal grafts were harvested, mRNA was isolated, and Foxp3 expression was analyzed using real-time PCR 14 days post-transplantation. n = 5. ( D ) DLNs were harvested, each DLN was stained for Foxp3 and CD4, and analyzed separately using flow cytometry. Mean fluorescence intensity (MFI) of Foxp3 levels by Tregs of low-risk and high-risk graft recipients was assesssed. N = 5 mice/group, data shown are representative of 3 independent experiments. ( E ) Treg suppression assay showing Treg suppressive function of Tregs isolated from DLNs of high-risk vs. low-risk recipients 14 days post-transplantation. Suppression of naïve BALB/c CD4 + CD25 − conventional T cell proliferation by Tregs was assessed following exposure to C57BL/6 (donor) or C3H (third party) APCs. All data were obtained from n = 5 mice/group and representative data from three independent experiments are shown. p values are calculated using the Mann-Whitney test and error bars represent SEM.

Journal: Scientific Reports

Article Title: Impaired Function of Peripherally Induced Regulatory T Cells in Hosts at High Risk of Graft Rejection

doi: 10.1038/srep39924

Figure Lengend Snippet: Corneal grafts were transplanted onto inflamed high-risk or control (‘low-risk’) host beds, and their corneas and draining lymph nodes (dLNs) were analyzed 14 days post-transplantation. ( A , B ) Corneal grafts were harvested and digested with collagenase D. Single cell suspensions were stained for Foxp3 and CD4, and analyzed using flow cytometry. 5 corneas per group were pooled for each analysis; data shown are representative of 3 independent experiments. ( C) Corneal grafts were harvested, mRNA was isolated, and Foxp3 expression was analyzed using real-time PCR 14 days post-transplantation. n = 5. ( D ) DLNs were harvested, each DLN was stained for Foxp3 and CD4, and analyzed separately using flow cytometry. Mean fluorescence intensity (MFI) of Foxp3 levels by Tregs of low-risk and high-risk graft recipients was assesssed. N = 5 mice/group, data shown are representative of 3 independent experiments. ( E ) Treg suppression assay showing Treg suppressive function of Tregs isolated from DLNs of high-risk vs. low-risk recipients 14 days post-transplantation. Suppression of naïve BALB/c CD4 + CD25 − conventional T cell proliferation by Tregs was assessed following exposure to C57BL/6 (donor) or C3H (third party) APCs. All data were obtained from n = 5 mice/group and representative data from three independent experiments are shown. p values are calculated using the Mann-Whitney test and error bars represent SEM.

Article Snippet: Real-time PCR was performed using a PCR mix (Taqman Universal PCR Master mix; Invitrogen) and preformulated primers for Foxp3 (Mm00475156_ml), IL-10 (Mm00439614_m1), IFN-γ (Mm00801778_m1), IL-12 (Mm00434165_m1), and Glyceraldehyde-3-Phosphate Dehydrogenase (GAPDH; Mm999999_gl) (Applied Biosystems, Austin, TX, USA).

Techniques: Control, Transplantation Assay, Staining, Flow Cytometry, Isolation, Expressing, Real-time Polymerase Chain Reaction, Fluorescence, Suppression Assay, MANN-WHITNEY

Proportions of total Tregs, nTregs and mTregs based on different gating strategies in whole blood and isolated CD4 + T cells of control subjects and post‐ACS and NSTE‐ACS patients

Journal: Journal of Internal Medicine

Article Title: Functional and homeostatic defects of regulatory T cells in patients with coronary artery disease

doi: 10.1111/joim.12398

Figure Lengend Snippet: Proportions of total Tregs, nTregs and mTregs based on different gating strategies in whole blood and isolated CD4 + T cells of control subjects and post‐ACS and NSTE‐ACS patients

Article Snippet: Quantitative real‐time PCR amplifications were performed with FAM‐labelled TaqMan primer/probe sets for FOXP3 (Hs01085834_m1) and GAPDH (Hs03929097_g1) as internal control (Life Technologies, Paisley, UK) using 1 μL of the preamplified cDNA.

Techniques: Isolation, Control

Expression of CTLA‐4 and CD39 in nTregs and mTregs from control subjects and post‐ACS and NSTE‐ACS patients

Journal: Journal of Internal Medicine

Article Title: Functional and homeostatic defects of regulatory T cells in patients with coronary artery disease

doi: 10.1111/joim.12398

Figure Lengend Snippet: Expression of CTLA‐4 and CD39 in nTregs and mTregs from control subjects and post‐ACS and NSTE‐ACS patients

Article Snippet: Quantitative real‐time PCR amplifications were performed with FAM‐labelled TaqMan primer/probe sets for FOXP3 (Hs01085834_m1) and GAPDH (Hs03929097_g1) as internal control (Life Technologies, Paisley, UK) using 1 μL of the preamplified cDNA.

Techniques: Expressing, Control

FOXP3 expression in nTregs and mTregs in control subjects and post‐ACS and NSTE‐ACS patients

Journal: Journal of Internal Medicine

Article Title: Functional and homeostatic defects of regulatory T cells in patients with coronary artery disease

doi: 10.1111/joim.12398

Figure Lengend Snippet: FOXP3 expression in nTregs and mTregs in control subjects and post‐ACS and NSTE‐ACS patients

Article Snippet: Quantitative real‐time PCR amplifications were performed with FAM‐labelled TaqMan primer/probe sets for FOXP3 (Hs01085834_m1) and GAPDH (Hs03929097_g1) as internal control (Life Technologies, Paisley, UK) using 1 μL of the preamplified cDNA.

Techniques: Expressing, Control