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Cd49c

Manufactured by BioLegend
Sourced in United States

CD49c is a cell surface antigen expressed on various cell types. It functions as an integrin subunit and plays a role in cell adhesion and migration processes.

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3 protocols using cd49c

1

Comprehensive Antibody Panel Profiling

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Antibodies were selected based on expected differences in expression levels among the 5 cell lines. The antibodies that were used belong to three different categories providing information of tissue origin, recognizing antigens involved in cell adhesion and potential drug targets. Anti-human EpCAM/CD326, Her2 and EGFR antibody were provided by Immunicon Corp. (Huntingdon Valley, Philadelphia, USA). Anti-human CD3, CD8a, CD11c, CD14, CD19, CD20, CD25, CD33, CD45, CD56, CD61, CD66b, CD105, CD123, CD140a, CD146, CD235a, CD71, CD117, CD221, CD227, CD261, CD262, CD309, Her3, CD24, CD44, CD49a, CD49b, CD49c, CD49d, CD49e, CD49f, CD103, CD104, CD106, CD113, CD144, CD166, CD324, CD334 antibodies were purchased from Biolegend Inc. (San Diego, CA, USA). Anti-human CD113 was purchased from Santa Cruz Biotechnology Inc. (Santa Cruz, CA, USA). Anti-human CD103 was purchased from BD Biosciences (San Jose, CA, USA). Anti-human serum albumin (HSA) antibody was used as a negative control in the SPRi experiments and was purchased from Sigma-Aldrich Chemie GmbH (Steinheim, Germany). Anti-mouse IgG PE was purchased from Abcam (Cambridge, UK) and was used for staining of unlabeled antibodies in flow cytometry and as a negative control in the SPRi experiments.
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2

Phenotypic Characterization of Bovine SDSCs

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The phenotype of bovine SDSCs at each passage (P1 to P4) was assessed by flow cytometry, as previously described17 (link). Cells were stained with antibodies against CD31 (endothelial cell marker, Thermo Scientific), CD34 (hematopoietic cell marker, Abcam), and mesenchymal markers CD49c (Thermo Scientific) and CD73 (BioLegend) 18 (link),19 ; positive MSC classification requires the absence of CD31 and CD34 and presence of CD7320 (link), while CD49c is a constant marker of chondrogenic potential of MSCs, decreasing only in the presence of TGF-β321 (link),22 (link). Cellular fluorescence was evaluated using a FACSCalibur flow cytometer (Becton Dickinson, Franklin Lakes, NJ) and the resulting data analyzed with FlowJo software (version 9.3.2).
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3

Evaluating Adhesion Molecule Expression in AECs

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Evaluation of plasma membrane adhesion molecule expression was performed in seven different cryopreserved AEC batches, using fluorochrome-conjugated monoclonal antibodies (as listed in Supplemental Table 2). Briefly, cells were exposed to antibodies directed against CD18 (Becton Dickinson; clone 6.7); CD29 (Becton Dickinson; clone 38047); CD49a (BioLegend; clone TS2/7); CD49c (BioLegend; clone ASC-1); CD49d (Becton Dickinson; clone 9F10); CD49e (Becton Dickinson; clone IIA1); CD49f (US Biologic; clone 7H164); CD51 (BioLegend; clone NKI-M9); CD61 (Becton Dickinson; clone VI-PL2); CD104 (BioLegend; clone 58XB4); beta5 integrin subunit (BioLegend; clone AST-3T); beta7 integrin subunit (BioLegend; FIB504). FITC-, PE- or APC-conjugated irrelevant isotype-matched monoclonal antibodies were purchased from Becton Dickinson or BioLegend. Cells were analysed with FACSCanto (Becton Dickinson) and data was shown as a percentage of positive cells.
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