cd45ro fitc Search Results


93
Miltenyi Biotec cd45ro
Immunophenotyping panel for multiplexed tissue imaging of cancer.
Cd45ro, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems fitc anti cd45ro
Immunophenotyping panel for multiplexed tissue imaging of cancer.
Fitc Anti Cd45ro, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Exbio Praha cd45ro-pe clone uchl1 antibody
Representative flow cytometric analysis of a hemodialysis patient. Representative dot plots depicting lymphocyte gating with B-lymphocytes (CD19+), and T lymphocytes (CD3+), CD4+ T cells, CD8+ T cells, naïve (CD45RA+) and memory <t>(CD45RO+)</t> T cell isoforms, naïve (CD4+CD45RA) T helper cells and memory (CD4+CD45RO) T helper cells, NK cells (CD3-CD16+CD56+) and NKT cells (CD3+CD16+CD56+).
Cd45ro Pe Clone Uchl1 Antibody, supplied by Exbio Praha, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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MBL International fitc-anti-cd45ro
Fig. 4. CD95 expression, susceptibility to apoptosis and CD95/ezrin co-localization in activated human primary T lymphocytes. (A) CD95 membrane expression and apoptosis were analyzed in electronically gated CD4+ by three-color immunofluorescence and FACS analysis in day 1- (upper panels) and day 6- (lower panels) activated human primary lymphocytes (PBL). Left panels are the CD95+/CD69+ CD4+ PBL; central panels are the <t>CD95+/CD45RO+</t> CD4+ lymphocytes; right panels are the apoptotic cells (FITC–annexin V+) CD4+ PBL after triggering with an anti-CD95 mAb (see Materials and methods). The results are representative of four experiments. (B) CD95 (green, FITC)/ezrin (red, TRITC) localization in day 1- (left panel) and day 6- (right panel) activated human primary T lymphocytes. In the upper and lower panels the single and double stainings are shown, respectively. Note the co-localization in day 6-activated lymphocytes, as revealed by the yellow staining (IVM) (magnification ×1000).
Fitc Anti Cd45ro, supplied by MBL International, 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/fitc-anti-cd45ro/product/MBL International
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QuantoBio cd45ro-fitc uchl1
Fig. 4. CD95 expression, susceptibility to apoptosis and CD95/ezrin co-localization in activated human primary T lymphocytes. (A) CD95 membrane expression and apoptosis were analyzed in electronically gated CD4+ by three-color immunofluorescence and FACS analysis in day 1- (upper panels) and day 6- (lower panels) activated human primary lymphocytes (PBL). Left panels are the CD95+/CD69+ CD4+ PBL; central panels are the <t>CD95+/CD45RO+</t> CD4+ lymphocytes; right panels are the apoptotic cells (FITC–annexin V+) CD4+ PBL after triggering with an anti-CD95 mAb (see Materials and methods). The results are representative of four experiments. (B) CD95 (green, FITC)/ezrin (red, TRITC) localization in day 1- (left panel) and day 6- (right panel) activated human primary T lymphocytes. In the upper and lower panels the single and double stainings are shown, respectively. Note the co-localization in day 6-activated lymphocytes, as revealed by the yellow staining (IVM) (magnification ×1000).
Cd45ro Fitc Uchl1, supplied by QuantoBio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Proimmune anti-cd45ro-fitc
Fig. 4. CD95 expression, susceptibility to apoptosis and CD95/ezrin co-localization in activated human primary T lymphocytes. (A) CD95 membrane expression and apoptosis were analyzed in electronically gated CD4+ by three-color immunofluorescence and FACS analysis in day 1- (upper panels) and day 6- (lower panels) activated human primary lymphocytes (PBL). Left panels are the CD95+/CD69+ CD4+ PBL; central panels are the <t>CD95+/CD45RO+</t> CD4+ lymphocytes; right panels are the apoptotic cells (FITC–annexin V+) CD4+ PBL after triggering with an anti-CD95 mAb (see Materials and methods). The results are representative of four experiments. (B) CD95 (green, FITC)/ezrin (red, TRITC) localization in day 1- (left panel) and day 6- (right panel) activated human primary T lymphocytes. In the upper and lower panels the single and double stainings are shown, respectively. Note the co-localization in day 6-activated lymphocytes, as revealed by the yellow staining (IVM) (magnification ×1000).
Anti Cd45ro Fitc, supplied by Proimmune, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biozol Diagnostica Vertrieb GmbH cd45ro (uchl1 fitc
Fig. 4. CD95 expression, susceptibility to apoptosis and CD95/ezrin co-localization in activated human primary T lymphocytes. (A) CD95 membrane expression and apoptosis were analyzed in electronically gated CD4+ by three-color immunofluorescence and FACS analysis in day 1- (upper panels) and day 6- (lower panels) activated human primary lymphocytes (PBL). Left panels are the CD95+/CD69+ CD4+ PBL; central panels are the <t>CD95+/CD45RO+</t> CD4+ lymphocytes; right panels are the apoptotic cells (FITC–annexin V+) CD4+ PBL after triggering with an anti-CD95 mAb (see Materials and methods). The results are representative of four experiments. (B) CD95 (green, FITC)/ezrin (red, TRITC) localization in day 1- (left panel) and day 6- (right panel) activated human primary T lymphocytes. In the upper and lower panels the single and double stainings are shown, respectively. Note the co-localization in day 6-activated lymphocytes, as revealed by the yellow staining (IVM) (magnification ×1000).
Cd45ro (Uchl1 Fitc, supplied by Biozol Diagnostica Vertrieb GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Miltenyi Biotec vimentin antibody, anti-human, fitc, reafinity
Fig. 4. CD95 expression, susceptibility to apoptosis and CD95/ezrin co-localization in activated human primary T lymphocytes. (A) CD95 membrane expression and apoptosis were analyzed in electronically gated CD4+ by three-color immunofluorescence and FACS analysis in day 1- (upper panels) and day 6- (lower panels) activated human primary lymphocytes (PBL). Left panels are the CD95+/CD69+ CD4+ PBL; central panels are the <t>CD95+/CD45RO+</t> CD4+ lymphocytes; right panels are the apoptotic cells (FITC–annexin V+) CD4+ PBL after triggering with an anti-CD95 mAb (see Materials and methods). The results are representative of four experiments. (B) CD95 (green, FITC)/ezrin (red, TRITC) localization in day 1- (left panel) and day 6- (right panel) activated human primary T lymphocytes. In the upper and lower panels the single and double stainings are shown, respectively. Note the co-localization in day 6-activated lymphocytes, as revealed by the yellow staining (IVM) (magnification ×1000).
Vimentin Antibody, Anti Human, Fitc, Reafinity, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Ancell corporation cd45ro-fitc
Fig. 4. CD95 expression, susceptibility to apoptosis and CD95/ezrin co-localization in activated human primary T lymphocytes. (A) CD95 membrane expression and apoptosis were analyzed in electronically gated CD4+ by three-color immunofluorescence and FACS analysis in day 1- (upper panels) and day 6- (lower panels) activated human primary lymphocytes (PBL). Left panels are the CD95+/CD69+ CD4+ PBL; central panels are the <t>CD95+/CD45RO+</t> CD4+ lymphocytes; right panels are the apoptotic cells (FITC–annexin V+) CD4+ PBL after triggering with an anti-CD95 mAb (see Materials and methods). The results are representative of four experiments. (B) CD95 (green, FITC)/ezrin (red, TRITC) localization in day 1- (left panel) and day 6- (right panel) activated human primary T lymphocytes. In the upper and lower panels the single and double stainings are shown, respectively. Note the co-localization in day 6-activated lymphocytes, as revealed by the yellow staining (IVM) (magnification ×1000).
Cd45ro Fitc, supplied by Ancell corporation, 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/cd45ro-fitc/product/Ancell corporation
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Caltag-Medsystems ltd cd45ro-fitc
Fig. 4. CD95 expression, susceptibility to apoptosis and CD95/ezrin co-localization in activated human primary T lymphocytes. (A) CD95 membrane expression and apoptosis were analyzed in electronically gated CD4+ by three-color immunofluorescence and FACS analysis in day 1- (upper panels) and day 6- (lower panels) activated human primary lymphocytes (PBL). Left panels are the CD95+/CD69+ CD4+ PBL; central panels are the <t>CD95+/CD45RO+</t> CD4+ lymphocytes; right panels are the apoptotic cells (FITC–annexin V+) CD4+ PBL after triggering with an anti-CD95 mAb (see Materials and methods). The results are representative of four experiments. (B) CD95 (green, FITC)/ezrin (red, TRITC) localization in day 1- (left panel) and day 6- (right panel) activated human primary T lymphocytes. In the upper and lower panels the single and double stainings are shown, respectively. Note the co-localization in day 6-activated lymphocytes, as revealed by the yellow staining (IVM) (magnification ×1000).
Cd45ro Fitc, supplied by Caltag-Medsystems ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Miltenyi Biotec cd20 cytoplasmic antibody, anti-human, fitc, reafinity
Fig. 4. CD95 expression, susceptibility to apoptosis and CD95/ezrin co-localization in activated human primary T lymphocytes. (A) CD95 membrane expression and apoptosis were analyzed in electronically gated CD4+ by three-color immunofluorescence and FACS analysis in day 1- (upper panels) and day 6- (lower panels) activated human primary lymphocytes (PBL). Left panels are the CD95+/CD69+ CD4+ PBL; central panels are the <t>CD95+/CD45RO+</t> CD4+ lymphocytes; right panels are the apoptotic cells (FITC–annexin V+) CD4+ PBL after triggering with an anti-CD95 mAb (see Materials and methods). The results are representative of four experiments. (B) CD95 (green, FITC)/ezrin (red, TRITC) localization in day 1- (left panel) and day 6- (right panel) activated human primary T lymphocytes. In the upper and lower panels the single and double stainings are shown, respectively. Note the co-localization in day 6-activated lymphocytes, as revealed by the yellow staining (IVM) (magnification ×1000).
Cd20 Cytoplasmic Antibody, Anti Human, Fitc, Reafinity, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Immunophenotyping panel for multiplexed tissue imaging of cancer.

Journal: Frontiers in Immunology

Article Title: Unveiling spatial complexity in solid tumor immune microenvironments through multiplexed imaging

doi: 10.3389/fimmu.2024.1383932

Figure Lengend Snippet: Immunophenotyping panel for multiplexed tissue imaging of cancer.

Article Snippet: CD45RO , UCHL1 , 50 , 130-113-549 , FITC , Miltenyi Biotec.

Techniques: Imaging

T cell subset classification and spatial distribution in an HCC sample. (A) Bar graph quantifications of gated T cell CD3 + T cells subpopulations (CD4 + T h , CD8 + T c , FoxP3 + /CD25 + T reg ) as well as T cell differentiation subsets (T N , T SCM , T CM , T EM , T EMRA , T TE ) for HCC tumor margin and tumor core. (B) Subclassification criteria used for T cell differentiation subset gating. Detailed gating scheme see <xref ref-type= Supplementary Figures S5A–D Spatial distribution of CD3+ T cell subsets as well as CD4+ and CD8+ differentiation subsets for tumor margin (C) and tumor core (D) . Arrowheads in (C, D) highlight the spatial distribution of regulatory T cells (T reg ). (E) Violin plots demonstrating expression levels of markers used for the definition of T cell differentiation subsets in tumor margin and tumor core: CD25, FoxP3, CD45RA, CD45RO, CD27, CD95, CD11a. Depicted markers and annotated cell types as indicated by the color code. ROI sizes: Tumor margin (ROI15) and tumor core (ROI16): 975 x 769 µm. " width="100%" height="100%">

Journal: Frontiers in Immunology

Article Title: Unveiling spatial complexity in solid tumor immune microenvironments through multiplexed imaging

doi: 10.3389/fimmu.2024.1383932

Figure Lengend Snippet: T cell subset classification and spatial distribution in an HCC sample. (A) Bar graph quantifications of gated T cell CD3 + T cells subpopulations (CD4 + T h , CD8 + T c , FoxP3 + /CD25 + T reg ) as well as T cell differentiation subsets (T N , T SCM , T CM , T EM , T EMRA , T TE ) for HCC tumor margin and tumor core. (B) Subclassification criteria used for T cell differentiation subset gating. Detailed gating scheme see Supplementary Figures S5A–D Spatial distribution of CD3+ T cell subsets as well as CD4+ and CD8+ differentiation subsets for tumor margin (C) and tumor core (D) . Arrowheads in (C, D) highlight the spatial distribution of regulatory T cells (T reg ). (E) Violin plots demonstrating expression levels of markers used for the definition of T cell differentiation subsets in tumor margin and tumor core: CD25, FoxP3, CD45RA, CD45RO, CD27, CD95, CD11a. Depicted markers and annotated cell types as indicated by the color code. ROI sizes: Tumor margin (ROI15) and tumor core (ROI16): 975 x 769 µm.

Article Snippet: CD45RO , UCHL1 , 50 , 130-113-549 , FITC , Miltenyi Biotec.

Techniques: Cell Differentiation, Expressing

Representative flow cytometric analysis of a hemodialysis patient. Representative dot plots depicting lymphocyte gating with B-lymphocytes (CD19+), and T lymphocytes (CD3+), CD4+ T cells, CD8+ T cells, naïve (CD45RA+) and memory (CD45RO+) T cell isoforms, naïve (CD4+CD45RA) T helper cells and memory (CD4+CD45RO) T helper cells, NK cells (CD3-CD16+CD56+) and NKT cells (CD3+CD16+CD56+).

Journal: Frontiers in Immunology

Article Title: The Humoral Immune Response to BNT162b2 Vaccine Is Associated With Circulating CD19+ B Lymphocytes and the Naïve CD45RA to Memory CD45RO CD4+ T Helper Cells Ratio in Hemodialysis Patients and Kidney Transplant Recipients

doi: 10.3389/fimmu.2021.760249

Figure Lengend Snippet: Representative flow cytometric analysis of a hemodialysis patient. Representative dot plots depicting lymphocyte gating with B-lymphocytes (CD19+), and T lymphocytes (CD3+), CD4+ T cells, CD8+ T cells, naïve (CD45RA+) and memory (CD45RO+) T cell isoforms, naïve (CD4+CD45RA) T helper cells and memory (CD4+CD45RO) T helper cells, NK cells (CD3-CD16+CD56+) and NKT cells (CD3+CD16+CD56+).

Article Snippet: The particular anti-human antibodies used were: CD3-FITC (Clone UCHT1), CD4-PE (Clone MEM-241), CD4-APC (Clone MEM-241), CD8-APC (Clone MEM-31), CD16-PE (Clone MEM-154), CD19-APC (Clone LT19), CD45-PerCP (Clone MEM-28), CD45RA-FITC (Clone MEM-56), CD45RO-PE (Clone UCHL1) and CD56-PE (Clone LT56), purchased from EXBIO, Praha SA.

Techniques:

Scatter plots representing individual values for each patient of the fraction of CD4+CD45RA/CD4+CD45RO T-helper cells and the percentage of CD19+ B cells respectively at baseline (T0), immediately before the second vaccine dose (T1) and 2 weeks after administration of the second dose (T2) in hemodialysis patients and kidney transplant recipients. HD, hemodialysis patients; KTRs, kidney transplant recipients.

Journal: Frontiers in Immunology

Article Title: The Humoral Immune Response to BNT162b2 Vaccine Is Associated With Circulating CD19+ B Lymphocytes and the Naïve CD45RA to Memory CD45RO CD4+ T Helper Cells Ratio in Hemodialysis Patients and Kidney Transplant Recipients

doi: 10.3389/fimmu.2021.760249

Figure Lengend Snippet: Scatter plots representing individual values for each patient of the fraction of CD4+CD45RA/CD4+CD45RO T-helper cells and the percentage of CD19+ B cells respectively at baseline (T0), immediately before the second vaccine dose (T1) and 2 weeks after administration of the second dose (T2) in hemodialysis patients and kidney transplant recipients. HD, hemodialysis patients; KTRs, kidney transplant recipients.

Article Snippet: The particular anti-human antibodies used were: CD3-FITC (Clone UCHT1), CD4-PE (Clone MEM-241), CD4-APC (Clone MEM-241), CD8-APC (Clone MEM-31), CD16-PE (Clone MEM-154), CD19-APC (Clone LT19), CD45-PerCP (Clone MEM-28), CD45RA-FITC (Clone MEM-56), CD45RO-PE (Clone UCHL1) and CD56-PE (Clone LT56), purchased from EXBIO, Praha SA.

Techniques:

Correlation between the humoral immune response with different lymphocyte subsets. The fraction of CD4+CD45RA/CD4+CD45RO (X-axis) has been plotted against the percentage of CD19+ cells (Y-axis) in kidney transplant recipients (circular points) and hemodialysis patients (square points) patients. The antibody counts following the first (0-100 grey, 101-500 green, 501-1500 yellow, >1500 red) and the second (different sizes from small to large from 0-30000) dose of vaccine were also depicted in each point. The results are presented for T0, T1 and T2 respectively. HD, hemodialysis patients; KTRs, kidney transplant recipients; HD, hemodialysis patients; KTRs, kidney transplant recipients.

Journal: Frontiers in Immunology

Article Title: The Humoral Immune Response to BNT162b2 Vaccine Is Associated With Circulating CD19+ B Lymphocytes and the Naïve CD45RA to Memory CD45RO CD4+ T Helper Cells Ratio in Hemodialysis Patients and Kidney Transplant Recipients

doi: 10.3389/fimmu.2021.760249

Figure Lengend Snippet: Correlation between the humoral immune response with different lymphocyte subsets. The fraction of CD4+CD45RA/CD4+CD45RO (X-axis) has been plotted against the percentage of CD19+ cells (Y-axis) in kidney transplant recipients (circular points) and hemodialysis patients (square points) patients. The antibody counts following the first (0-100 grey, 101-500 green, 501-1500 yellow, >1500 red) and the second (different sizes from small to large from 0-30000) dose of vaccine were also depicted in each point. The results are presented for T0, T1 and T2 respectively. HD, hemodialysis patients; KTRs, kidney transplant recipients; HD, hemodialysis patients; KTRs, kidney transplant recipients.

Article Snippet: The particular anti-human antibodies used were: CD3-FITC (Clone UCHT1), CD4-PE (Clone MEM-241), CD4-APC (Clone MEM-241), CD8-APC (Clone MEM-31), CD16-PE (Clone MEM-154), CD19-APC (Clone LT19), CD45-PerCP (Clone MEM-28), CD45RA-FITC (Clone MEM-56), CD45RO-PE (Clone UCHL1) and CD56-PE (Clone LT56), purchased from EXBIO, Praha SA.

Techniques:

Fig. 4. CD95 expression, susceptibility to apoptosis and CD95/ezrin co-localization in activated human primary T lymphocytes. (A) CD95 membrane expression and apoptosis were analyzed in electronically gated CD4+ by three-color immunofluorescence and FACS analysis in day 1- (upper panels) and day 6- (lower panels) activated human primary lymphocytes (PBL). Left panels are the CD95+/CD69+ CD4+ PBL; central panels are the CD95+/CD45RO+ CD4+ lymphocytes; right panels are the apoptotic cells (FITC–annexin V+) CD4+ PBL after triggering with an anti-CD95 mAb (see Materials and methods). The results are representative of four experiments. (B) CD95 (green, FITC)/ezrin (red, TRITC) localization in day 1- (left panel) and day 6- (right panel) activated human primary T lymphocytes. In the upper and lower panels the single and double stainings are shown, respectively. Note the co-localization in day 6-activated lymphocytes, as revealed by the yellow staining (IVM) (magnification ×1000).

Journal:

Article Title: CD95 (APO-1/Fas) linkage to the actin cytoskeleton through ezrin in human T lymphocytes: a novel regulatory mechanism of the CD95 apoptotic pathway

doi: 10.1093/emboj/19.19.5123

Figure Lengend Snippet: Fig. 4. CD95 expression, susceptibility to apoptosis and CD95/ezrin co-localization in activated human primary T lymphocytes. (A) CD95 membrane expression and apoptosis were analyzed in electronically gated CD4+ by three-color immunofluorescence and FACS analysis in day 1- (upper panels) and day 6- (lower panels) activated human primary lymphocytes (PBL). Left panels are the CD95+/CD69+ CD4+ PBL; central panels are the CD95+/CD45RO+ CD4+ lymphocytes; right panels are the apoptotic cells (FITC–annexin V+) CD4+ PBL after triggering with an anti-CD95 mAb (see Materials and methods). The results are representative of four experiments. (B) CD95 (green, FITC)/ezrin (red, TRITC) localization in day 1- (left panel) and day 6- (right panel) activated human primary T lymphocytes. In the upper and lower panels the single and double stainings are shown, respectively. Note the co-localization in day 6-activated lymphocytes, as revealed by the yellow staining (IVM) (magnification ×1000).

Article Snippet: After this time cells were incubated at 4°C with saturating concentration of directly conjugated: (i) FITC-anti-CD69, PE-anti-CD95 (MBL International Corporation, Watertown, USA) PerCP-anti-CD4; (ii) FITC-anti-CD45RO, PE-anti-CD95, PerCP-anti-CD4; and (iii) isotype matched normal FITC, PE and PerCP Ab (Becton Dickinson, Mountain View, CA).

Techniques: Expressing, Immunofluorescence, Staining