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3 protocols using anti alb

1

Immunofluorescence Staining Protocol

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Cells were fixed with 4% paraformaldehyde diluted in PBS for 20 min and permeabilized with 0.1% Triton-X 100 diluted in PBS for 10 min at room temperature. Then cells were blocked in 10% goat serum with 1% bovine serum albumin (BSA) for 60 min on the shaker, followed by anti-HBc (Austral, United States), anti-HA (Sigma, United States), anti-nanog (Santa Cruz, Dallas, TX, United States), anti-FoxA2 (Sigma-Aldrich, St. Louis, MO, United States), anti-HNF4a (Cell Signaling), anti-AFP (Sigma-Aldrich, St. Louis, MO, United States) or anti-ALB (Cedarlane, Burlington, Canada) antibodies in 1:500 dilution with 1% BSA in PBS incubated at 4°C over night. The next day, the primary antibody was washed away and the 594 or 488 fluorescent anti-rabbit secondary antibody and 5 mg/ml 4′,6-DAPI with 1:20,000 dilution were added and incubated at 37°C for 30 min. Then, after washing the secondary antibody away, the cells were observed by fluorescent microscopy (Wu X. et al., 2012 (link)).
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2

Immunofluorescence and Western Blot Analyses

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The following antibodies were used for immunofluorescence staining or western blot analyses: anti-FoxA2 (used at 1:400, Cell Signaling), anti-HNF4α (used at 1:500, Cell Signaling), anti-AFP (used at 1:1000, Sigma-Aldrich), anti-ALB (used at 1:1000, Cedarlane, Burlington, Canada), anti-ZO-1 (used at 1:1000, Thermo Fisher), anti-E cadherin (used at 1:500, Cell Signaling), anti-SR-BI (used at 1:100, Novus Biologicals), anti-BCRP (used at 1:100, Millipore), anti-MRP2 EAG548 (link) (used at 1:200, a kind gift from Anne Nies, IKP Stuttgart48 (link)), anti-Apo-CIII (used at 1:500, Abcam), anti-CYP8B1 (used at 1:100, Abcam), anti-ORF2 (used at 1:400, a kind gift from Suzanne U. Emerson, NIH) and anti-HAV capsid (used at 1:1000, a kind gift from Stanley M. Lemon, UNC School of Medicine). Alexa Fluor 488 and 549 anti-mouse (used at 1:1000) and Alexa Fluor 488 and 549 anti-rabbit (used at 1:1000) antibodies were purchased from ThermoFisher. Alexa 594-conjugated transferrin was purchased from ThermoFisher. Tenofovir, Tenofovir disoproxil fumarate, and Emtricitabine were obtained through the AIDS Reagent Program, Division of AIDS, NIAID, NIH. Elvitegravir and Cobicistat were purchased from SelleckChem. Sofosbuvir was purchased from Acme Bioscience. BX795, oleic acid and lomitapide were purchased from Sigma-Aldrich.
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3

Immunofluorescence and Western Blot Analysis

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The following antibodies were used for immunofluorescence staining: anti-OCT3/4 (Stemgent, Cambridge, MA), anti-SEEA4 (Stemcell Technologies, Vancouver, Canada), anti-GATA4 (Cell Signaling, Danvers, MA), anti-HNF4α (Cell Signaling), anti-AFP (Sigma-Aldrich, St. Louis, MO), anti-ALB (Cedarlane, Burlington, Canada), and anti-ORF2 (a kind gift from Suzanne U. Emerson, NIH). The following antibodies were used for Western blot (WB) analysis: anti-HCV NS5A clone 9E1018 (link), anti-CypA (Santa Cruz, Dallas, TX), and anti-actin HRP (Sigma-Aldrich). IFN-β was purchased from pBL Assay Science (Piscataway, NJ), Sofosbuvir from Acme Bioscience (Palo Alto, CA), and Cyclosporin A, Ribavirin and BX795 from Sigma-Aldrich. Activin-A, Wnt-3A and oncostatin-M were purchased from R&D Systems (Minneapolis, MN), bFGF from Life Technologies, and BMP-4, EGF and HGF were purchased from Peprotech (Rocky Hill, NJ).
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