Figure A. PE conjugated Mouse anti Human CD45RO and Amethyst Orange conjugated Mouse IgG1 isotype control . Figure B. PE conjugated Mouse anti Human CD3 and Amethyst Orange conjugated Mouse anti Human CD45RA . All experiments performed on human blood gated on live single lymphocytes, in the presence of 10% human serum. Data acquired on the ZE5 Cell Analyzer
Figure A. PE-Cy5 conjugated mouse anti human CD45RO and FITC conjugated Mouse IgG1 isotype control . Figure B. PE-Cy5 conjugated mouse anti human CD45RO and FITC conjugated mouse anti human CD45RA . All experiments performed on red cell lysed human peripheral blood gated on lymphocytes in the presence of Human SeroBlock
Figure A. RPE conjugated mouse anti human CD45RO and PE-A647 conjugated mouse IgG1 isotype control . Figure B. RPE conjugated mouse anti human CD45RO and PE-A647 conjugated mouse anti Human CD45RA . All experiments performed on red cell lysed human blood gated on lymphocytes. Data acquired on the ZE5 cell analyzer.
Figure A. RPE conjugated mouse anti human CD45RO and A647 conjugated mouse IgG1 isotype control . Figure B. RPE conjugated mouse anti human CD45RO and A647 conjugated mouse anti Human CD45RA . All experiments performed on red cell lysed human blood gated on lymphocytes. Data acquired on the ZE5 cell analyzer.
Staining of formalin fixed, paraffin embedded human tonsil with Mouse anti Human CD45RA
AlexaFluor 700 conjugated Mouse anti Human CD45RA antibody used for the phenotypic characterization of CD8 expressing T cells by flow cytometry.
Image caption:
CD8 T cell subpopulation distribution in the blood and endocervix.
(A) A diagram of Sallusto and Lanzavecchia’s classification scheme of CD8 T cells based on CD45RA and CCR7 expression and relative perforin expression of the different subpopulation, (B) distribution of the different CD8 T cell subpopulations in a representative C. trachomatis-negative and C. trachomatis-positive women (C-D) Distribution of different CD8 T cells in the blood (C), and in the endocervix (D) of 16 women (n=16). Using flow cytometric analyses, CD8 T cells were identified in a population of cells from PBMC and endocervical cells by gating for CD3+CD8+ cells. CD8 T cells were further characterized based on CD45RA and CCR7 expression. Naïve cells are CD45RA+ CCR7+, central memory (TCM) cells are CD45RA-CCR7+, effector memory (TEM) cells are CD45RA- CCR7-, and terminally differentiated effector memory (TEMRA) cells are CD45RA+ CCR7-. The majority of CD8 T cells in the endocervix are TEM CD8 subtype.
From: Ibana JA, Myers L, Porretta C, Lewis M, Taylor SN, Martin DH, Quayle AJ.
The major CD8 T cell effector memory subset in the normal and Chlamydia trachomatis-infected human endocervix is low in perforin.
BMC Immunol. 2012 Dec 7;13:66.