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4 protocols using anti gfp ab32146

1

Western Blotting Assay for Protein Detection

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For western blotting assay, protein samples of strains were prepared and extracted as described previously [96 (link)]. Proteins separated on the SDS-PAGE gel were transferred onto a polyvinylidene fluoride membrane with a Bio-Rad electroblotting apparatus. The polyclonal anti-Flag A9044 (Sigma, St. Louis, MO, USA), monoclonal anti-GFP ab32146 (Abcam, Cambridge, MA, USA) and monoclonal anti-mCherry ab125096 (Abcam, Cambridge, UK) antibodies were used at a 1:2000 to 1:10000 dilution for immunoblot assays. The samples were also detected with the monoclonal anti-GAPDH antibody EM1101 (Hangzhou HuaAn Biotechnology co., Ltd.) as a reference. Incubation with a secondary antibody and chemiluminescent detection were performed as described previously [97 (link)]. The experiment was repeated three times independently.
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2

Immunoblot Analysis of Fungal Signaling Proteins

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Fresh mycelia (200 mg) of each strain were finely ground and suspended in 1 ml of extraction buffer (50 mM Tris-HCl, pH7.5, 100 mM NaCl, 5 mM EDTA, 1% Triton X-100, 2 mM PMSF) and 10 μl of protease inhibitor cocktail (Sangon Co., Shanghai, China). After homogenization with a vortex shaker, the lysate was centrifuged at 10 000 g in a microcentrifuge for 20 min at 4°C. The resulting proteins were separated on 10% denaturating polyacrylamide gel (SDS-PAGE) and transferred to Immobilon-P transfer membrane (Millipore, Billerica, MA, USA) with a Bio-Rad electroblotting apparatus. The monoclonal anti-GFP ab32146 (Abcam, Cambridge, MA, USA) antibody was used at a 1:5000 to 1:10000 dilution for BcMkk1-GFP immunoblot assays. The phosphorylated BcBmp1 and BcBmp3 were detected with phospho-p44/42 MAPK antibody (Cell Signaling Technology, Boston, MA, USA). The total BcBmp1 and BcBmp3 were detected using p44/42 MAPK antibody (Cell Signaling Technology Inc., Beverly, MA, USA) and anti-Mpk1 antibody (Santa Cruz Biotechnology, Santa Cruz, CA, USA), respectively. Incubation with a secondary antibody and chemiluminescent detection were performed as described previously [92 (link)]. The experiment was conducted three times independently.
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3

Investigating Smad Signaling in HEK 293T Cells

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HEK 293T cells (provided by Prof. Yixiang Wang) were cultured in Dulbecco’s Modified Eagle Medium (DMEM, Life Technologies, CA, USA) supplemented with 10% fetal bovine serum (FBS, Invitrogen, CA, USA) and 1% penicillin/streptomycin (Life Technologies) at 37°C in a humidified atmosphere of 5% CO2. Cells were transiently transfected with either the WT and mutant plasmids (V205A and H251Y) using Lipo3000 (Invitrogen, CA, USA), and then collected for western blot analysis. 20 μg protein of each sample was resolved by SDS-PAGE and transferred onto a polyvinylidene difluoride membrane. Blots were probed with the following antibodies: anti-GFP (ab32146, Abcam, Cambridge, UK), phospho-Smad 1/5/9 (13820, Cell Signaling Technology, MA, USA), total Smad 1/5 (bs-2973R, Bioss Biotechnology, Beijing, China) and GAPDH (KM9002T, Sungene Biotech, Tianjin, China). Protein densitometry was quantified using Image J software and normalized against the housekeeping protein, GAPDH.
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4

Protein Isolation and Immunoblot Analysis

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The protein isolation was performed as described previously [67 (link)]. The resulting proteins were separated by 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred to Immobilon-P transfer membrane (Millipore, Billerica, MA, USA). The polyclonal anti-Flag A9044 (Sigma, St. Louis, MO) and monoclonal anti-GFP ab32146 (Abcam, Cambridge, UK) antibodies were used at a 1:5000 to 1:10 000 dilution for immunoblot analyses. The samples were also detected with monoclonal anti-GAPDH antibody EM1101 (Hangzhou HuaAn Biotechnology Co., Ltd.) as a reference. The intensity of immunoblot bands were quantified using the ImageQuantTL software.
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