The largest database of trusted experimental protocols

4 protocols using cd3 apc

1

Four-Color Flow Cytometry for CD19 CAR T-Cell Detection

Check if the same lab product or an alternative is used in the 5 most similar protocols
A four-color flow cytometry panel was designed using a commercial CD19 CAR Detection Reagent (Miltenyi Biotec, Bergisch Gladbach, Germany). The reagent consists of a biotinylated CD19 antigen that specifically binds CD19-targeted CARs. In a second incubation step the biotin-labeled CAR T cells are then stained with a fluorochrome-conjugated anti-biotin antibody.
In brief, 200 µl whole blood were treated for 10 min with 2 ml of NH4Cl-based erythrocyte lysing solution (Beckman Coulter, Krefeld, Germany) and washed with PBS, containing 0.5% HSA. After removal of the supernatant down to 200 µl, cells were resuspended and 100 µl were transferred to a new flow cytometry tube. Following 15 min of incubation with 1 µl CD19 CAR Detection Reagent, cells were washed twice and incubated for 15 min with 1 µl Anti-Biotin-PE (Miltenyi Biotec, Bergisch Gladbach, Germany), 10 µl 7-AAD, 5 µl CD3-APC, and 5 µl CD45-KrO (all purchased from Beckman Coulter Immunotech, Marseille, France). After a final washing step, cells were acquired on a NAVIOS flow cytometer (Beckman Coulter, Krefeld, Germany). Cellular debris was excluded based on light scatter properties and CAR T cells were defined as 7-AAD-/CD45+/mononuclear cells/CD3+/CD19 CAR+ (Supplementary Figure 1).
+ Open protocol
+ Expand
2

Multiparametric Flow Cytometry Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
For reference, see Stepensky et al. (2013) (link). Additional antibodies used in the study were TCR αβ FITC, CD3 APC, CD16/CD56 PE, CD8 AF700, CD45RA PE, CD38 Pacific Blue, CD20 PerCp, IgG APC, kappa FITC, lambda PE, CD21 FITC, CD8 PE, and TCR γδ PE (Beckman Coulter GmbH); CD45RA APC-Cy7 and IL-2 PerCpCy5.5 (BioLegend Inc.); CD27 FITC, CD27 APC, CD27 BV605, CD27 PerCpCy5.5, CD38 APC, CD19 APC, IgG PE, S6(pS235/236) APC (BD Biosciences), and IgM AF488 (Jackson); and BclXL AF488 (Cell Signaling Technologies).
+ Open protocol
+ Expand
3

Multiparametric T Cell Phenotyping

Check if the same lab product or an alternative is used in the 5 most similar protocols
The following antibodies were used in this study for T cell phenotyping: CD3-PerCP (clone SK7/Cat# 347344), CD25-APC AF700, CD4-Krome Orange (13B8.2/A96417), CD8-Pacific Blue (B9.11/A82791), CD3-APC (Beckman Coulter Inc. Brea, CA), Rat Anti-Mouse IgG1-APC (X56/550874) (BD Biosciences, San Jose, CA). PD-1-Percp Cy7 and TIM3-APC (BD Biosciences, San Jose, CA) were used as markers of T cell exhaustion. MUC1 antigen expression by tumor cells was measured using anti-MUC1, (Santa Cruz Biotechnology. Inc., Dallas, TX). CAR molecules were detected using Goat anti-human F(ab’)2 antibody conjugated with AlexaFluor647 (109–606-097) (Jackson ImmunoResearch Laboratories, Inc., West Grove, PA). Cells were stained with saturating amounts of antibody (~5uL) for 20 min at 4 °C, washed (PBS, Sigma-Alrich, St. Louis, MO), and then acquired on Gallios™ Flow Cytometer (Beckman Coulter Inc., Brea, CA). Analysis was performed using Kaluza® Flow Analysis Software (Beckman Coulter Inc.).
+ Open protocol
+ Expand
4

T Cell Co-culture Assay with CAPAN-1

Check if the same lab product or an alternative is used in the 5 most similar protocols
T cells were co-cultured with 0.5×106 CAPAN-1 PSCA/TGFβ/IL4 producing cell line at the specified effector:target ratio in 4 mL complete media in a 6-well plate. The cells were harvested every 3 days, labeled with CD3 APC, CD4 Krome Orange and CD8 Pacific blue antibodies (Beckman Coulter) and quantified by flow cytometer using CountBrightTM Absolute Counting Beads (approximately 0.2×105 beads/20 μL added to each condition) (Invitrogen, Eugene, OR) and 5 μL of 7-AAD (BD Biosciences) to exclude dead cells. Total tumor and T cell numbers were back calculated from the viable cell numbers obtained by terminating acquisition at 2,000 beads.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!