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Found 3 matching solutions for this experiment
Upstream tips |
Protocol tips |
Downstream tips |
Single cell suspensions were stained with fluorescently conjugated antibodies in a 1:100 dilution unless otherwise noted. Cells were stained with LIVE/DEAD™ Aqua or Blue (Invitrogen), blocked with 4μg/ml anti-CD16/32 (2.4G2; Bioxcell) |
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Samples were analyzed on an LSRII and sorted on an Aria II cell sorter (BD Biosciences). |
Upstream tips |
Single cell suspensions were stained with fluorescently conjugated antibodies in a 1:100 dilution unless otherwise noted. Cells were stained with LIVE/DEAD™ Aqua or Blue (Invitrogen), blocked with 4μg/ml anti-CD16/32 (2.4G2; Bioxcell) |
Downstream tips |
Samples were analyzed on an LSRII and sorted on an Aria II cell sorter (BD Biosciences). |
Upstream tips |
Protocol tips |
Downstream tips |
Single cell suspensions were stained with fluorescently conjugated antibodies in a 1:100 dilution unless otherwise noted. Cells were stained with LIVE/DEAD™ Aqua or Blue (Invitrogen), blocked with 4μg/ml anti-CD16/32 (2.4G2; Bioxcell) |
|
Samples were analyzed on an LSRII and sorted on an Aria II cell sorter (BD Biosciences). |
Upstream tips |
Single cell suspensions were stained with fluorescently conjugated antibodies in a 1:100 dilution unless otherwise noted. Cells were stained with LIVE/DEAD™ Aqua or Blue (Invitrogen), blocked with 4μg/ml anti-CD16/32 (2.4G2; Bioxcell) |
Downstream tips |
Samples were analyzed on an LSRII and sorted on an Aria II cell sorter (BD Biosciences). |
Upstream tips |
Protocol tips |
Downstream tips |
mice were sacrificed and spleens were used for preparing single-cell suspensions by mechanical dissociation followed by removal of red blood cells with ammonium chloride lysis buffer (ACK). |
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Upstream tips |
mice were sacrificed and spleens were used for preparing single-cell suspensions by mechanical dissociation followed by removal of red blood cells with ammonium chloride lysis buffer (ACK). |
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