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Mouse α pd l1

Manufactured by Thermo Fisher Scientific
Sourced in United States

Mouse α-PD-L1 is a monoclonal antibody that binds to the PD-L1 (programmed death-ligand 1) protein expressed on the surface of certain cells. This antibody is commonly used in research applications to investigate the role of the PD-1/PD-L1 pathway in various biological processes.

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2 protocols using mouse α pd l1

1

Comprehensive Immunological Profiling of PD-L1 Expression

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Immunofluorescence: mouse α-EEA1 (1G11, eBioscience), mouse α-PD-L1 (MIH1, eBioscience), rabbit α-PD-L1 (EPFR19759, Abcam), mouse α-LAMP1 (H4A4, eBioscience), mouse α-Calnexin (AF18, Abcam), mouse α-GM130 (169276, Abcam), mouse α-TGN46 (2F7.1, Abcam), mouse α-Rab11 (47/Rab11, BD Transduction Laboratories), mouse α-TfR (236-15375, Thermo-Fisher), rabbit α-CMTM6 (HPA026980, Sigma-Aldrich).
Flow Cytometry: FITC mouse IgG2a κ isotype control (MOPC-173, Biolegend), APC mouse IgG2b κ isotype control (MPC-11, Biolegend), APC mouse IgG1 κ isotype control (MOPC-21), APC mouse α-PD-L1 (29E.2A3, Biolegend), APC mouse α-PD-L1 (MIH1, eBioscience), Alexa Fluor 488 rabbit α-PD-L1 (Abcam), APC mouse α-HLA-ABC (W6/32), Alexa Fluor 488 mouse α-HLA-ABC (W6/32, Biolegend), FITC mouse α-CD8 (HIT8a, BD Pharmingen), PE-Cy7 mouse α-TNFα (MAb11, eBioscience), APC mouse α-PD-1 (J105, eBioscience), PerCp-Cy5.5 mouse α-Perforin (B-D48, Biolegend).
Immunoprecipitation/Immunoblotting: goat anti-PDL1 (AF156, R&D Systems), rabbit α-PD-L1 (E1L3N, Cell Signalling Technology), mouse α-PD-L1 (405.9A11, Cell Signalling Technology), mouse α-PD-L1 (MIH1, eBioScience), rabbit α-CMTM6 (Sigma-Aldrich, HPA026980).
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2

Immunogold Labeling of Exosomal PD-L1

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In order to obtain the TEM images for identification of exosomal surface proteins, gold nanoparticles (5–10 nm in diameter) have been extensively used.[8, 16] In this study, exosomal PD‐L1 was observed using TEM with immunogold labeling, as reported previously.[8a] Briefly, the purified EXOs were deposited onto pure carbon‐coated grids. For immunogold labeling, EXOs were treated with mouse αPD‐L1 (eBioscience, 14‐5983‐82, San Diego, CA, USA), followed by incubation with antimouse IgG‐conjugated 5 nm gold particles (Sigma‐Aldrich, G7527). After staining with 2% uranyl acetate, the grids were dried at 25 °C and visualized at 100 kV using a Hitachi HT‐7700 TEM (Tokyo, Japan).
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