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Bio-Rad cd25
Proportions of regulatory and conventional CD4 T cells in BALC. A – D The percentages of Tconv and Treg CD4 cells in the BALC were determined using flow cytometry. (A, B) presents the percentages within total CD3 + CD4 + cells. A Shows CD4 + <t>CD25</t> −/low Foxp3 − Tconv cells. B Shows CD4 + CD25 high Foxp3 + Treg cells. C , D Shows the percentages of ICOS + Ki-67 + within the respective parental population of C Tconv and D Treg. Statistical analysis was performed using the Mann–Whitney unpaired, non-parametric test, (*) p < 0.05 or (**) p < 0.01 (mean; n = 5).
Cd25, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 88 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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1) Product Images from "Swine influenza A virus infection sets the local immunological landscape in subsequent infection with porcine reproductive and respiratory syndrome virus"

Article Title: Swine influenza A virus infection sets the local immunological landscape in subsequent infection with porcine reproductive and respiratory syndrome virus

Journal: Veterinary Research

doi: 10.1186/s13567-025-01536-6

Proportions of regulatory and conventional CD4 T cells in BALC. A – D The percentages of Tconv and Treg CD4 cells in the BALC were determined using flow cytometry. (A, B) presents the percentages within total CD3 + CD4 + cells. A Shows CD4 + CD25 −/low Foxp3 − Tconv cells. B Shows CD4 + CD25 high Foxp3 + Treg cells. C , D Shows the percentages of ICOS + Ki-67 + within the respective parental population of C Tconv and D Treg. Statistical analysis was performed using the Mann–Whitney unpaired, non-parametric test, (*) p < 0.05 or (**) p < 0.01 (mean; n = 5).
Figure Legend Snippet: Proportions of regulatory and conventional CD4 T cells in BALC. A – D The percentages of Tconv and Treg CD4 cells in the BALC were determined using flow cytometry. (A, B) presents the percentages within total CD3 + CD4 + cells. A Shows CD4 + CD25 −/low Foxp3 − Tconv cells. B Shows CD4 + CD25 high Foxp3 + Treg cells. C , D Shows the percentages of ICOS + Ki-67 + within the respective parental population of C Tconv and D Treg. Statistical analysis was performed using the Mann–Whitney unpaired, non-parametric test, (*) p < 0.05 or (**) p < 0.01 (mean; n = 5).

Techniques Used: Flow Cytometry, MANN-WHITNEY



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Image Search Results


Proportions of regulatory and conventional CD4 T cells in BALC. A – D The percentages of Tconv and Treg CD4 cells in the BALC were determined using flow cytometry. (A, B) presents the percentages within total CD3 + CD4 + cells. A Shows CD4 + CD25 −/low Foxp3 − Tconv cells. B Shows CD4 + CD25 high Foxp3 + Treg cells. C , D Shows the percentages of ICOS + Ki-67 + within the respective parental population of C Tconv and D Treg. Statistical analysis was performed using the Mann–Whitney unpaired, non-parametric test, (*) p < 0.05 or (**) p < 0.01 (mean; n = 5).

Journal: Veterinary Research

Article Title: Swine influenza A virus infection sets the local immunological landscape in subsequent infection with porcine reproductive and respiratory syndrome virus

doi: 10.1186/s13567-025-01536-6

Figure Lengend Snippet: Proportions of regulatory and conventional CD4 T cells in BALC. A – D The percentages of Tconv and Treg CD4 cells in the BALC were determined using flow cytometry. (A, B) presents the percentages within total CD3 + CD4 + cells. A Shows CD4 + CD25 −/low Foxp3 − Tconv cells. B Shows CD4 + CD25 high Foxp3 + Treg cells. C , D Shows the percentages of ICOS + Ki-67 + within the respective parental population of C Tconv and D Treg. Statistical analysis was performed using the Mann–Whitney unpaired, non-parametric test, (*) p < 0.05 or (**) p < 0.01 (mean; n = 5).

Article Snippet: CD25 , K231.3B2 , Mouse IgG1 , A647 , 1/10 , Bio-Rad.

Techniques: Flow Cytometry, MANN-WHITNEY

Fig. 5. Representative immunohistochemistry staining of CD4, CD8, and CD25 in corneal allografts. The numbers of the cells

Journal: Frontiers in bioscience (Landmark edition)

Article Title: Mesenchymal stem cell derived exosomes-based immunological signature in a rat model of corneal allograft rejection therapy.

doi: 10.31083/j.fbl2703086

Figure Lengend Snippet: Fig. 5. Representative immunohistochemistry staining of CD4, CD8, and CD25 in corneal allografts. The numbers of the cells

Article Snippet: Subsequently, sections were pre-blocked with 5% goat serum albumin for 30 min and incubated with mouse anti-CD4, anti-CD8, anti-CD25 overnight at 4 ◦C (Mouse anti Rat CD4 (MCA55GA, 1:50, AbD Serotec), Mouse anti Rat CD8 (MCA48GA, 1:500, AbD Serotec), Mouse anti Rat CD25 (MCA273GA, 1:100, AbD Serotec).

Techniques: Immunohistochemistry, Staining

Fig. 6. Flow cytometry was used for analysis of proportion of CD4+CD25+Foxp3+Tregs. Splenocytes from recipient rats were

Journal: Frontiers in bioscience (Landmark edition)

Article Title: Mesenchymal stem cell derived exosomes-based immunological signature in a rat model of corneal allograft rejection therapy.

doi: 10.31083/j.fbl2703086

Figure Lengend Snippet: Fig. 6. Flow cytometry was used for analysis of proportion of CD4+CD25+Foxp3+Tregs. Splenocytes from recipient rats were

Article Snippet: Subsequently, sections were pre-blocked with 5% goat serum albumin for 30 min and incubated with mouse anti-CD4, anti-CD8, anti-CD25 overnight at 4 ◦C (Mouse anti Rat CD4 (MCA55GA, 1:50, AbD Serotec), Mouse anti Rat CD8 (MCA48GA, 1:500, AbD Serotec), Mouse anti Rat CD25 (MCA273GA, 1:100, AbD Serotec).

Techniques: Flow Cytometry

Antibodies used for flow cytometry and brain immunohistochemistry analysis in rat

Journal: American Journal of Physiology - Heart and Circulatory Physiology

Article Title: Elevated bone marrow sympathetic drive precedes systemic inflammation in angiotensin II hypertension

doi: 10.1152/ajpheart.00510.2018

Figure Lengend Snippet: Antibodies used for flow cytometry and brain immunohistochemistry analysis in rat

Article Snippet: 9 , Mouse anti-rat CD25:RPE , FC , Bio-Rad , mca273pe.

Techniques: Flow Cytometry, Immunohistochemistry

Antibodies used for flow cytometry and brain immunohistochemistry analysis in rat

Journal: American Journal of Physiology - Heart and Circulatory Physiology

Article Title: Elevated bone marrow sympathetic drive precedes systemic inflammation in angiotensin II hypertension

doi: 10.1152/ajpheart.00510.2018

Figure Lengend Snippet: Antibodies used for flow cytometry and brain immunohistochemistry analysis in rat

Article Snippet: All samples were read using an LSR-II (BD Biosystems) at the University of Florida Interdisciplinary Center for Biotechnology, and the data were analyzed with FACSDiva software, version 6.1.2. table ft1 table-wrap mode="anchored" t5 Table 1. caption a7 Antibody Application Vendor Reference No. 1 Mmouse anti-NeuN IHC Millipore Sigma MAB377 2 Anti-Iba1 IHC Wako Laboratory 019-19741 3 Mouse anti-rat CD4 IHC ebioscience 14-0040-82 4 Mouse anti-rat CD68:Alexa Fluor 647 FC Bio-Rad mca341a647 6 Mouse anti-rat CD5:Alexa Fluor 647 FC Bio-Rad mca52a647 7 Mouse anti-rat CD8 ALPHA:Alexa Fluor 647 FC Bio-Rad mca48a647 8 Anti-Mouse/Rat CD90.1 (Thy-1.1) PerCP-Cyanine5.5 FC ebioscience 45-0900-80 9 Mouse anti-rat CD25:RPE FC Bio-Rad mca273pe 10 Mouse anti-rat CD3:Alexa Fluor 647 FC Bio-Rad mca772a647 11 Anti-Rat CD45 FITC, OXO1 FC ebioscience 11-0461-82 13 Anti-Mouse/Rat IL-17A Alexa Fluor 488 FC ebioscience 537177-81 14 Mouse anti-rat CD68:RPE FC Bio-Rad mca341pe 15 Mouse anti-rat CD4 647 FC Bio-Rad mca55ga Open in a separate window FC, flow cytometry; IHC, immunohistochemistry.

Techniques: Flow Cytometry, Immunohistochemistry

Central administration of ANG II is associated with elevated bone marrow (BM) and circulating inflammatory markers. Intracerebroventricular (ICV) ANG II increased levels of CD4+.IL17+ T cells in the blood (A and B) and BM (C) at day 7, as measured by flow cytometry. In addition, levels of several other T cell subtypes (CD4+.CD25+, CD3+, CD3+.CD45+, and CD68+ macrophage/monocytes were increased in the BM at day 7 of ANG II infusion (C), as measured by flow cytometry. Dennervation of the femoral BM sympathetic nerve (BM SNX) at day 7 of ICV ANG II infusion significantly reduced the ANG II-dependent increase in the inflammatory cells in the BM (C), suggesting BM sympathetic nerve activity-dependent activation of BM immune system by ANG II, as measured by flow cytometry. Real-time PCR showed elevated levels of several inflammatory markers, including TLR4, HIF1a, and ITGAM, in the BM at day 7 of ANG II infusion (D), which was reduced by BM SNX (left); significant elevation in several adrenergic receptors in the BM at day 21 of ANG II infusion, as measured by real-time PCR (right). Data are presented as means ± SE, n = 6; *P < 0.05 vs. control; #P < 0.05 vs. day 7; ANOVA.

Journal: American Journal of Physiology - Heart and Circulatory Physiology

Article Title: Elevated bone marrow sympathetic drive precedes systemic inflammation in angiotensin II hypertension

doi: 10.1152/ajpheart.00510.2018

Figure Lengend Snippet: Central administration of ANG II is associated with elevated bone marrow (BM) and circulating inflammatory markers. Intracerebroventricular (ICV) ANG II increased levels of CD4+.IL17+ T cells in the blood (A and B) and BM (C) at day 7, as measured by flow cytometry. In addition, levels of several other T cell subtypes (CD4+.CD25+, CD3+, CD3+.CD45+, and CD68+ macrophage/monocytes were increased in the BM at day 7 of ANG II infusion (C), as measured by flow cytometry. Dennervation of the femoral BM sympathetic nerve (BM SNX) at day 7 of ICV ANG II infusion significantly reduced the ANG II-dependent increase in the inflammatory cells in the BM (C), suggesting BM sympathetic nerve activity-dependent activation of BM immune system by ANG II, as measured by flow cytometry. Real-time PCR showed elevated levels of several inflammatory markers, including TLR4, HIF1a, and ITGAM, in the BM at day 7 of ANG II infusion (D), which was reduced by BM SNX (left); significant elevation in several adrenergic receptors in the BM at day 21 of ANG II infusion, as measured by real-time PCR (right). Data are presented as means ± SE, n = 6; *P < 0.05 vs. control; #P < 0.05 vs. day 7; ANOVA.

Article Snippet: All samples were read using an LSR-II (BD Biosystems) at the University of Florida Interdisciplinary Center for Biotechnology, and the data were analyzed with FACSDiva software, version 6.1.2. table ft1 table-wrap mode="anchored" t5 Table 1. caption a7 Antibody Application Vendor Reference No. 1 Mmouse anti-NeuN IHC Millipore Sigma MAB377 2 Anti-Iba1 IHC Wako Laboratory 019-19741 3 Mouse anti-rat CD4 IHC ebioscience 14-0040-82 4 Mouse anti-rat CD68:Alexa Fluor 647 FC Bio-Rad mca341a647 6 Mouse anti-rat CD5:Alexa Fluor 647 FC Bio-Rad mca52a647 7 Mouse anti-rat CD8 ALPHA:Alexa Fluor 647 FC Bio-Rad mca48a647 8 Anti-Mouse/Rat CD90.1 (Thy-1.1) PerCP-Cyanine5.5 FC ebioscience 45-0900-80 9 Mouse anti-rat CD25:RPE FC Bio-Rad mca273pe 10 Mouse anti-rat CD3:Alexa Fluor 647 FC Bio-Rad mca772a647 11 Anti-Rat CD45 FITC, OXO1 FC ebioscience 11-0461-82 13 Anti-Mouse/Rat IL-17A Alexa Fluor 488 FC ebioscience 537177-81 14 Mouse anti-rat CD68:RPE FC Bio-Rad mca341pe 15 Mouse anti-rat CD4 647 FC Bio-Rad mca55ga Open in a separate window FC, flow cytometry; IHC, immunohistochemistry.

Techniques: Flow Cytometry, Activity Assay, Activation Assay, Real-time Polymerase Chain Reaction