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2 protocols using violetfluor450 α cd3

1

Isolation and Immunophenotyping of Peritoneal Exudate Cells

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Peritoneal exudate cells (PECs) were collected by lavage with 10 mL of flow buffer (1% FBS in PBS (Corning)). PECs were washed once, then Fc receptors were blocked with α-CD16/32 (Biolegend). The following antibodies were used in various experiments: Alexafluor 647-α-CD102 (3C4 (MIC2/4), Biolegend), APC-Cy7-α-CD19 (1D3, BD Biosciences), redFluor 710-α-CD11b (M1/70, Tonbo), Fitc-α-CD11b (M1/70, BD Biosciences), PE-Cy7-α-CD19 (1D3, Tonbo), Violetfluor450-α-CD3 (17A2, Tonbo), and BV711-α-Siglec F (E50-2440, BD Biosciences). Cells were fixed with 2% formaldehyde (VWR). Samples were run on a Novoctye 3000 (ACEA Biosciences) and analyzed with either Flowjo (Tree Star, Inc, San Carols, CA) or NovoExpress (version 1.5.0, Agilent Technologies, Inc.).
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2

Isolation and Immunophenotyping of Peritoneal Exudate Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Peritoneal exudate cells (PECs) were collected by lavage with 10 mL of flow buffer (1% FBS in PBS (Corning)). PECs were washed once, then Fc receptors were blocked with α-CD16/32 (Biolegend). The following antibodies were used in various experiments: Alexafluor 647-α-CD102 (3C4 (MIC2/4), Biolegend), APC-Cy7-α-CD19 (1D3, BD Biosciences), redFluor 710-α-CD11b (M1/70, Tonbo), Fitc-α-CD11b (M1/70, BD Biosciences), PE-Cy7-α-CD19 (1D3, Tonbo), Violetfluor450-α-CD3 (17A2, Tonbo), and BV711-α-Siglec F (E50-2440, BD Biosciences). Cells were fixed with 2% formaldehyde (VWR). Samples were run on a Novoctye 3000 (ACEA Biosciences) and analyzed with either Flowjo (Tree Star, Inc, San Carols, CA) or NovoExpress (version 1.5.0, Agilent Technologies, Inc.).
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