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Thy 1 apc

Manufactured by BD
Sourced in Germany

THY-1-APC is a fluorochrome-conjugated antibody designed for the detection of the Thy-1 (CD90) antigen. Thy-1 is a glycosylphosphatidylinositol (GPI)-anchored glycoprotein expressed on the surface of various cell types, including T cells, neurons, and hematopoietic stem cells. The APC (Allophycocyanin) fluorochrome attached to the antibody allows for the visualization and analysis of Thy-1-positive cells using flow cytometry or other fluorescence-based techniques.

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2 protocols using thy 1 apc

1

Immunophenotyping of Cultured Cells

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Digested cells were suspended in HBSS at a density of 1–5 × 107 cells/mL and stained for 30 minutes on ice with THY-1-APC (BD Pharmingen) and LNGFR-PE (Miltenyi Biotec) antibodies for sorting. Cultured cells (at three and five passages) were harvested using cell-dissociation buffer (Gibco). Cells (1.0 × 105) were suspended in ice-cold HBSS and stained for 30 minutes on ice with the monoclonal antibodies CD45-PE-Cy7 (Tonbo Biosciences), CD29-PE, CD31-PE-Cy7, CD44-PE, CD105-PE and CD166-PE (BioLegend) for cell surface analysis. Flow cytometric analysis and cell sorting were performed on a triple-laser Moflo system (Beckman Coulter) and data were analyzed using Flowjo software (Tree Star).
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2

Isolation and Sorting of Human Bone Marrow Cells

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All BM‐MNC experiments were performed using Poietics BM‐MNCs purchased from LONZA. Ethical approval for the generation of these cells was comprehensively undertaken by LONZA. hMSCs were prepared from human BM (human BM‐MNCs; Lonza, Amagazaki, Japan) as described in our previous report and in the Supplemental Experimental Procedures.30, 35 All experimental protocols were approved by the animal committee of Keio University, Japan. All methods were conducted in strict accordance with the approved guidelines of the institutional animal care committee. LNGFR‐PE (Miltenyi Biotec, Bergisch‐Gladbach, Germany) and THY‐1‐APC (BD Pharmingen, San Jose, California) were added to the human BM cells and incubated for 30 minutes on ice. The tube was centrifuged, the supernatant was discarded, and HBSS containing propidium iodide (Sigma, St. Louis, Missouri) was added. The cells were sorted using a triple‐laser MoFlo (Beckman Coulter, Brea, California), FACS Vantage SE, or FACS Aria III (Becton Dickinson, Bedford, Massachusetts). The data were analyzed using FlowJo software (Tree Star, Ashland, Oregon). All flow cytometry experiments are described in the Supplemental Experimental Procedures.
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