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5 protocols using apc anti human egfr antibody

1

EGFR Kinase Inhibitors Modulate C. albicans Infection

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The EGFR kinase domain inhibitors were purchased from Santa Cruz (Gefitinib), Selleckchem (PD153035), Tocris Bioscience (AG1478) and Sigma (GW2974). Marimastat, GI-253023X, glibenclamide and Bapta-AM were purchased from Tocris Bioscience. Inhibitors were reconstituted in DMSO and aliquoted for appropriate freezer temperature storage. TR146 cells were incubated with inhibitors for 1 h prior to C. albicans infection, candidalysin exposure or mock treatment. Phospho-EGFR Tyr1068 (#3777), phospho-EGFR Tyr845 (#6963S), c-Fos (#2250S) and phospho-MKP1 (#2857S) antibodies were purchased from Cell Signalling Technology. Mouse anti-human α-actin antibody was purchased from Millipore (UK) (#MAB1501), goat anti-mouse (#115-035-062) and anti-rabbit (#111-035-144) horseradish peroxidase (HRP)-conjugated antibodies were purchased from Jackson Immunologicals (Stratech Scientific, UK). Fluorescent ErbB receptor affibodies were a kind gift from the Science and Technologies Facilities Council for use with confocal imaging work. APC anti-human EGFR antibody was purchased from BioLegend (# 352905) for use with Imagestream analyses. Biologically active EREG and EPG were purchased from Peprotech and used at 10, 25 and 50 ng/mL either individually or together at the same concentration.
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2

Flow Cytometric Analysis of EGFR Expression

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APC anti‐human EGFR Antibody (352905, BioLegend) was used for flow cytometry. The cells were collected in a tube and washed three times with PBS. Then, the cells were incubated with the fluorescently labelled antibody at room temperature for 30 min in the dark. After incubation, the antibody solution was removed by centrifuging the cells at 200g and re‐suspending them in PBS. Finally, the cells were analysed on a flow cytometer (BD Bioscience).
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3

Antibody and Reagent Specifications for Cell Signaling Experiments

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Puromycin and G-418 were purchased from Cayman Chemical (Ann Arbor, Michigan, USA). AG1478, and U0126 were purchased from Selleck. The protein A/G agarose and EGF were purchased from Sigma (St louis, MO, USA). The following antibodies were used: anti-β-actin (#8457), anti-cleaved-caspase-3 (#9664), ani-caspase-3 (#9662), anti-cleaved PARP (#5625), anti-EGFR (#4267), anti-Erk1/2 (#4695), anti-phospho-Erk1/2 (#4370), anti-p38 (#8690), anti-phospho-p38 (#9211), anti-AKT(#9272), anti-phospho-AKT (Ser473) (#4060), anti-phospho-JNK (Thr183/Tyr185) (#9251), anti-JNK (#9252), anti-HA-Tag (#3724), anti-c-Cbl (#2747), anti-ubiquitin (P4D1) (#3936) from Cell Signaling Technology (Beverly, MA, USA); anti-Flag-Tag from Sigma-Aldrich (St Louis, MO, USA), anti-GAPDH (AC002), anti-phospho-EGFR (Y1068) (AP0820) from Abclonal Technology(Shanghai, China); anti-14-3-3σ (ab14123), anti-Bim (ab7888) from Abcam (Cambridge, MA, USA); anti-Bcl-2 (12789-1-AP) from proteintech (Chicago, IL, USA); Alexa Flour 488-conjugated anti- rabbit IgG, Alexa Flour 555-conjugated anti-rabbit IgG and Alexa Flour 555-conjugated anti-mouse IgG from Thermo Scientific (Rockford, IL, USA). HRP conjugated anti-rabbit IgG, HRP conjugated anti-mouse IgG from Beyotime Institute of Biotechnology; APC anti-human EGFR antibody (#352905) used for cell surface immunofluorescence staining from BioLegend (San Diego, CA).
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4

Multiparametric Flow Cytometry for Cell Analysis

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Flow cytometry was performed using the
MACSQuant Analyzer 10 or MACSQuant X (Miltenyi Biotec). All flow cytometry
data was analyzed using FlowJo v.7.6.2 software (Tree Star Inc., Ashland,
OR). Cell staining was carried out by incubation with PBS containing
the recommended concentration of antibodies at RT for 30 min. PBS
washes were carried out between antibody staining. Cell viability
was determined using viability dye SYTOX Blue Dead Cell Stain (ThermoFisher)
prior to flow cytometric analysis. Cells were first gated for singlet
population identified by FSC-H and FSC-A. Next, live cells were identified
using a viability dye, followed by gating for target cell populations.
The antibodies used in the study are as follows: CD3 PECy7 (Biolegend,
317334), Human CD34 APC-conjugated antibody (R&D system, FAB7227A),
Human CD34 Alexa Fluor 488-conjugated antibody (R&D system, FAB7227G),
Streptavidin PE (Biolegend, 405204), APC antihuman EGFR antibody (Biolegend,
352905), Alexa Fluor 488 antihuman EGFR antibody (Biolegend, 352907),
PE anti-HA.11 Epitope Tag antibody (Biolegend, 901517), Anti-M13-HRP
(Sino Biologics, 1197 mm05T-H), Anti-Myc-HRP (Genscript, A00863),
and SYTOX Blue Dead Cell Stain (ThermoFisher, S10274).
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5

EGFR Internalization and Surface Expression

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Cells were grown in DMEM with 10% FBS for 14 h and then were serum starved for 24 h before treating with EGF. For the assay of internalization of EGFR, the serum-starved cells were fixed with 4% paraformaldehyde after stimulated with EGF for the indicated time points. After that, cells were used in immunofluorescence assay. For flow cytometry analysis of cell surface expression levels of EGFR, cells were trypsinized and collected after incubating with EGF at the indicated time points. After washing twice with cold PBS, cells without permeation were incubated with APC anti-human EGFR Antibody (352905, BioLegend, San Diego, CA) for 30 min. After washing, cells were immediately subjected to the flow cytometry analysis.
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