cd45ro antibody Search Results


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FIGURE 5. Memory T cells are more sensitive to Pam3CSK4, flagellin, and R-848 than naive T cells. Naive (CD45RA) () and memory <t>(CD45RO)</t> T cells (u) were purified from CD4 T cells by FACS sorting and either unstimulated or stimulated with IL-2 (100 U/ml for cytokine production or 20 U/ml for proliferation assay) or anti-CD2 mAbs (2 g/ml) in the absence or presence of 1 g/ml Pam3CSK4, 5 g/ml flagellin, or 1 g/ml R-848. IFN- was quantified in the 48-h cell-free supernatants (A), and proliferation was determined after 72 h (B). Results are expressed as mean SD, n 3, and are representative of the data obtained with the T cells of two of six healthy donors.
Anti Cd45ro Mab, 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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FIGURE 5. Memory T cells are more sensitive to Pam3CSK4, flagellin, and R-848 than naive T cells. Naive (CD45RA) () and memory <t>(CD45RO)</t> T cells (u) were purified from CD4 T cells by FACS sorting and either unstimulated or stimulated with IL-2 (100 U/ml for cytokine production or 20 U/ml for proliferation assay) or anti-CD2 mAbs (2 g/ml) in the absence or presence of 1 g/ml Pam3CSK4, 5 g/ml flagellin, or 1 g/ml R-848. IFN- was quantified in the 48-h cell-free supernatants (A), and proliferation was determined after 72 h (B). Results are expressed as mean SD, n 3, and are representative of the data obtained with the T cells of two of six healthy donors.
Anti Cd45ro, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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FIGURE 5. Memory T cells are more sensitive to Pam3CSK4, flagellin, and R-848 than naive T cells. Naive (CD45RA) () and memory <t>(CD45RO)</t> T cells (u) were purified from CD4 T cells by FACS sorting and either unstimulated or stimulated with IL-2 (100 U/ml for cytokine production or 20 U/ml for proliferation assay) or anti-CD2 mAbs (2 g/ml) in the absence or presence of 1 g/ml Pam3CSK4, 5 g/ml flagellin, or 1 g/ml R-848. IFN- was quantified in the 48-h cell-free supernatants (A), and proliferation was determined after 72 h (B). Results are expressed as mean SD, n 3, and are representative of the data obtained with the T cells of two of six healthy donors.
Anti Cd45ro Pe, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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FIGURE 5. Memory T cells are more sensitive to Pam3CSK4, flagellin, and R-848 than naive T cells. Naive (CD45RA) () and memory <t>(CD45RO)</t> T cells (u) were purified from CD4 T cells by FACS sorting and either unstimulated or stimulated with IL-2 (100 U/ml for cytokine production or 20 U/ml for proliferation assay) or anti-CD2 mAbs (2 g/ml) in the absence or presence of 1 g/ml Pam3CSK4, 5 g/ml flagellin, or 1 g/ml R-848. IFN- was quantified in the 48-h cell-free supernatants (A), and proliferation was determined after 72 h (B). Results are expressed as mean SD, n 3, and are representative of the data obtained with the T cells of two of six healthy donors.
Apc Vio770 Anti Cd45ro, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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FIGURE 5. Memory T cells are more sensitive to Pam3CSK4, flagellin, and R-848 than naive T cells. Naive (CD45RA) () and memory <t>(CD45RO)</t> T cells (u) were purified from CD4 T cells by FACS sorting and either unstimulated or stimulated with IL-2 (100 U/ml for cytokine production or 20 U/ml for proliferation assay) or anti-CD2 mAbs (2 g/ml) in the absence or presence of 1 g/ml Pam3CSK4, 5 g/ml flagellin, or 1 g/ml R-848. IFN- was quantified in the 48-h cell-free supernatants (A), and proliferation was determined after 72 h (B). Results are expressed as mean SD, n 3, and are representative of the data obtained with the T cells of two of six healthy donors.
Anti Human Cd45ro Apc Vio770, 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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Immune cell subpopulations in untreated tumor-bearing animals detected by Chipcytometry (n = 3).
Cd45ro, 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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Miltenyi Biotec anti biotin multi sort
Immune cell subpopulations in untreated tumor-bearing animals detected by Chipcytometry (n = 3).
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Immune cell subpopulations in untreated tumor-bearing animals detected by Chipcytometry (n = 3).
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Comparison of immunophenotypes between CAR.MUC1-41BB ζ and CAR.MUC1-CD28 ζ . The phenotypic analyses of CAR T cells were performed on days 4, 11, and 14 after transduction. (a) Representative flow cytometry plot demonstrating the cell subset analyzed with fluorochrome-conjugated anti-CD3 and anti-CD56 on day 4 after T cell transduction. (b) Bar graph represents the percentage of CD3 + T cells (mean ± S.E.M from 8 donors). (c) Representative flow cytometry plot at 4 and 11 after transduction. (d) Mean percentage of CD8 + : CD4 + ratio on day 4 and day 11 after transduction is shown. Data shown are mean ± S.E.M from 6 donors. (e) Representative flow cytometry analysis of memory phenotype analyzed on days 4, 11, and 14 after transduction; CAR T cells were expanded in culture media containing IL-2 50 U/ml and stained with <t>anti-CD45RO</t> and anti-CD62L antibody (TEM: CD45RO + CD62L − , TCM: CD45RO + CD62L + , TN: CD45RO − CD62L + , and TE: CD45RO − CD62L − ). (f) The mean percentage of naïve (TN), central memory (TCM), effector memory (TEM), and terminal effector (TE) T cells. Data represents as mean ± S.E.M ( n = 6).
Cd45ro Apc, 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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Comparison of immunophenotypes between CAR.MUC1-41BB ζ and CAR.MUC1-CD28 ζ . The phenotypic analyses of CAR T cells were performed on days 4, 11, and 14 after transduction. (a) Representative flow cytometry plot demonstrating the cell subset analyzed with fluorochrome-conjugated anti-CD3 and anti-CD56 on day 4 after T cell transduction. (b) Bar graph represents the percentage of CD3 + T cells (mean ± S.E.M from 8 donors). (c) Representative flow cytometry plot at 4 and 11 after transduction. (d) Mean percentage of CD8 + : CD4 + ratio on day 4 and day 11 after transduction is shown. Data shown are mean ± S.E.M from 6 donors. (e) Representative flow cytometry analysis of memory phenotype analyzed on days 4, 11, and 14 after transduction; CAR T cells were expanded in culture media containing IL-2 50 U/ml and stained with <t>anti-CD45RO</t> and anti-CD62L antibody (TEM: CD45RO + CD62L − , TCM: CD45RO + CD62L + , TN: CD45RO − CD62L + , and TE: CD45RO − CD62L − ). (f) The mean percentage of naïve (TN), central memory (TCM), effector memory (TEM), and terminal effector (TE) T cells. Data represents as mean ± S.E.M ( n = 6).
Apc Conjugated Cd45ro Mab, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


FIGURE 5. Memory T cells are more sensitive to Pam3CSK4, flagellin, and R-848 than naive T cells. Naive (CD45RA) () and memory (CD45RO) T cells (u) were purified from CD4 T cells by FACS sorting and either unstimulated or stimulated with IL-2 (100 U/ml for cytokine production or 20 U/ml for proliferation assay) or anti-CD2 mAbs (2 g/ml) in the absence or presence of 1 g/ml Pam3CSK4, 5 g/ml flagellin, or 1 g/ml R-848. IFN- was quantified in the 48-h cell-free supernatants (A), and proliferation was determined after 72 h (B). Results are expressed as mean SD, n 3, and are representative of the data obtained with the T cells of two of six healthy donors.

Journal: Journal of immunology (Baltimore, Md. : 1950)

Article Title: Direct stimulation of human T cells via TLR5 and TLR7/8: flagellin and R-848 up-regulate proliferation and IFN-gamma production by memory CD4+ T cells.

doi: 10.4049/jimmunol.175.3.1551

Figure Lengend Snippet: FIGURE 5. Memory T cells are more sensitive to Pam3CSK4, flagellin, and R-848 than naive T cells. Naive (CD45RA) () and memory (CD45RO) T cells (u) were purified from CD4 T cells by FACS sorting and either unstimulated or stimulated with IL-2 (100 U/ml for cytokine production or 20 U/ml for proliferation assay) or anti-CD2 mAbs (2 g/ml) in the absence or presence of 1 g/ml Pam3CSK4, 5 g/ml flagellin, or 1 g/ml R-848. IFN- was quantified in the 48-h cell-free supernatants (A), and proliferation was determined after 72 h (B). Results are expressed as mean SD, n 3, and are representative of the data obtained with the T cells of two of six healthy donors.

Article Snippet: CD4 CD45RO T cells were separated into CCR7 and CCR7 cells by FACS sorting using FITC-labeled anti-CD45RO mAb and PE-labeled antiCCR7 mAb (R&D Systems).

Techniques: Proliferation Assay

Immune cell subpopulations in untreated tumor-bearing animals detected by Chipcytometry (n = 3).

Journal: International Journal of Molecular Sciences

Article Title: In-Depth Immune-Oncology Studies of the Tumor Microenvironment in a Humanized Melanoma Mouse Model

doi: 10.3390/ijms22031011

Figure Lengend Snippet: Immune cell subpopulations in untreated tumor-bearing animals detected by Chipcytometry (n = 3).

Article Snippet: 10 , 5 , CD45RO , REA611 , 130-113-559 , PE , Miltenyi Biotech.

Techniques:

Multiplex staining Chipcytometry.

Journal: International Journal of Molecular Sciences

Article Title: In-Depth Immune-Oncology Studies of the Tumor Microenvironment in a Humanized Melanoma Mouse Model

doi: 10.3390/ijms22031011

Figure Lengend Snippet: Multiplex staining Chipcytometry.

Article Snippet: 10 , 5 , CD45RO , REA611 , 130-113-559 , PE , Miltenyi Biotech.

Techniques: Multiplex Assay, Staining, Marker

Comparison of immunophenotypes between CAR.MUC1-41BB ζ and CAR.MUC1-CD28 ζ . The phenotypic analyses of CAR T cells were performed on days 4, 11, and 14 after transduction. (a) Representative flow cytometry plot demonstrating the cell subset analyzed with fluorochrome-conjugated anti-CD3 and anti-CD56 on day 4 after T cell transduction. (b) Bar graph represents the percentage of CD3 + T cells (mean ± S.E.M from 8 donors). (c) Representative flow cytometry plot at 4 and 11 after transduction. (d) Mean percentage of CD8 + : CD4 + ratio on day 4 and day 11 after transduction is shown. Data shown are mean ± S.E.M from 6 donors. (e) Representative flow cytometry analysis of memory phenotype analyzed on days 4, 11, and 14 after transduction; CAR T cells were expanded in culture media containing IL-2 50 U/ml and stained with anti-CD45RO and anti-CD62L antibody (TEM: CD45RO + CD62L − , TCM: CD45RO + CD62L + , TN: CD45RO − CD62L + , and TE: CD45RO − CD62L − ). (f) The mean percentage of naïve (TN), central memory (TCM), effector memory (TEM), and terminal effector (TE) T cells. Data represents as mean ± S.E.M ( n = 6).

Journal: Journal of Immunology Research

Article Title: An In Vitro Comparison of Costimulatory Domains in Chimeric Antigen Receptor T Cell for Breast Cancer Treatment

doi: 10.1155/2022/2449373

Figure Lengend Snippet: Comparison of immunophenotypes between CAR.MUC1-41BB ζ and CAR.MUC1-CD28 ζ . The phenotypic analyses of CAR T cells were performed on days 4, 11, and 14 after transduction. (a) Representative flow cytometry plot demonstrating the cell subset analyzed with fluorochrome-conjugated anti-CD3 and anti-CD56 on day 4 after T cell transduction. (b) Bar graph represents the percentage of CD3 + T cells (mean ± S.E.M from 8 donors). (c) Representative flow cytometry plot at 4 and 11 after transduction. (d) Mean percentage of CD8 + : CD4 + ratio on day 4 and day 11 after transduction is shown. Data shown are mean ± S.E.M from 6 donors. (e) Representative flow cytometry analysis of memory phenotype analyzed on days 4, 11, and 14 after transduction; CAR T cells were expanded in culture media containing IL-2 50 U/ml and stained with anti-CD45RO and anti-CD62L antibody (TEM: CD45RO + CD62L − , TCM: CD45RO + CD62L + , TN: CD45RO − CD62L + , and TE: CD45RO − CD62L − ). (f) The mean percentage of naïve (TN), central memory (TCM), effector memory (TEM), and terminal effector (TE) T cells. Data represents as mean ± S.E.M ( n = 6).

Article Snippet: For cell surface marker analysis, the following antibodies were used: CD56-PE (HCD56/Cat#130-114-551), CD4-FITC (OKT4/130-114-531), CD8-APC (SK1/130-110-679), CD45RO-APC (UCHL1/130-113-556), CD62L-FITC (DREG-56/130-112-077), CD25-APC (BC96/130-113-284) (Miltenyi Biotec, Bergisch Gladbach, Germany), PD1-FITC (EH12.2H7/329904), LAG-3-FITC (11C3C65/369308), TIM-3-APC (F38-2E2/345012), and CD3-PerCP (clone OKT3/317336) (BioLegend, San Diego, CA, USA).

Techniques: Comparison, Transduction, Flow Cytometry, Staining