Purification:Article Title: Deciphering melanophagy: role of the PTK2-ITCH-MLANA-OPTN cascade on melanophagy in melanocytes
Article Snippet: After 24 h, the cells were homogenized and pulled down with anti-MYC-agarose (Santa Cruz Biotechnology, SC-40 AC) via the same methods with immunoprecipitation section. .. Purified MYC or MYC-ITCH were incubated with reaction solution (0.1 μM E1 [Abcam, ab139467], 6.6 μg UBE2L3/UBCH7 [R&D system, E2-640-100], 1.25 μg MLANA protein [Proteintech, Ag13387], 2.5 μM Ub [Abcam, ab139467], 0.02 U/μl inorganic pyrophosphatase solution [ThermoFisher, EF0221], 1 mm dithiothreitol [ThermoFisher, R0861], 0.1 M Mg-ATP [Abcam, ab139467], 5 mm EDTA [GenDEPOT, P3100–001]) at 37°C for 2 h. After incubation, the reaction was terminated with 2X non-reducing gel loading buffer (Abcam, ab139467), and the ubiquitination was analyzed with western blotting. .. B16F1 cells were washed twice with 37°C phosphate-buffered saline (PBS; WELGENE, LB001–02) and fixed with 4% paraformaldehyde (Biosesang, PC2031–100) for 15 min at room temperature.
Article Title: Deciphering melanophagy: role of the PTK2-ITCH-MLANA-OPTN cascade on melanophagy in melanocytes.
Article Snippet: After 24 h, the cells were homogenized and pulled down with anti-MYC-agarose (Santa Cruz Biotechnology, SC-40 AC) via the same methods with immunoprecipitation section. .. Purified MYC or MYC-ITCH were incubated with reaction solution (0.1 μM E1 [Abcam, ab139467], 6.6 μg UBE2L3/UBCH7 [R&D system, E2-640-100], 1.25 μg MLANA protein [Proteintech, Ag13387], 2.5 μM Ub [Abcam, ab139467], 0.02 U/μl inorganic pyrophosphatase solution [ThermoFisher, EF0221], 1 mM dithiothreitol [ThermoFisher, R0861], 0.1 M Mg-ATP [Abcam, ab139467], 5 mM EDTA [GenDEPOT, P3100-001]) at 37°C for 2 h. After incubation, the reaction was terminated with 2X non-reducing gel loading buffer (Abcam, AC CE PT ED M AN US CR IP T ab139467), and the ubiquitination was analyzed with western blotting. .. B16F1 cells were washed twice with 37°C phosphate-buffered saline (PBS; WELGENE, LB001-02) and fixed with 4% paraformaldehyde (Biosesang, PC2031-100) for 15 min at room temperature.
Incubation:Article Title: Deciphering melanophagy: role of the PTK2-ITCH-MLANA-OPTN cascade on melanophagy in melanocytes
Article Snippet: After 24 h, the cells were homogenized and pulled down with anti-MYC-agarose (Santa Cruz Biotechnology, SC-40 AC) via the same methods with immunoprecipitation section. .. Purified MYC or MYC-ITCH were incubated with reaction solution (0.1 μM E1 [Abcam, ab139467], 6.6 μg UBE2L3/UBCH7 [R&D system, E2-640-100], 1.25 μg MLANA protein [Proteintech, Ag13387], 2.5 μM Ub [Abcam, ab139467], 0.02 U/μl inorganic pyrophosphatase solution [ThermoFisher, EF0221], 1 mm dithiothreitol [ThermoFisher, R0861], 0.1 M Mg-ATP [Abcam, ab139467], 5 mm EDTA [GenDEPOT, P3100–001]) at 37°C for 2 h. After incubation, the reaction was terminated with 2X non-reducing gel loading buffer (Abcam, ab139467), and the ubiquitination was analyzed with western blotting. .. B16F1 cells were washed twice with 37°C phosphate-buffered saline (PBS; WELGENE, LB001–02) and fixed with 4% paraformaldehyde (Biosesang, PC2031–100) for 15 min at room temperature.
Article Title: Deciphering melanophagy: role of the PTK2-ITCH-MLANA-OPTN cascade on melanophagy in melanocytes.
Article Snippet: After 24 h, the cells were homogenized and pulled down with anti-MYC-agarose (Santa Cruz Biotechnology, SC-40 AC) via the same methods with immunoprecipitation section. .. Purified MYC or MYC-ITCH were incubated with reaction solution (0.1 μM E1 [Abcam, ab139467], 6.6 μg UBE2L3/UBCH7 [R&D system, E2-640-100], 1.25 μg MLANA protein [Proteintech, Ag13387], 2.5 μM Ub [Abcam, ab139467], 0.02 U/μl inorganic pyrophosphatase solution [ThermoFisher, EF0221], 1 mM dithiothreitol [ThermoFisher, R0861], 0.1 M Mg-ATP [Abcam, ab139467], 5 mM EDTA [GenDEPOT, P3100-001]) at 37°C for 2 h. After incubation, the reaction was terminated with 2X non-reducing gel loading buffer (Abcam, AC CE PT ED M AN US CR IP T ab139467), and the ubiquitination was analyzed with western blotting. .. B16F1 cells were washed twice with 37°C phosphate-buffered saline (PBS; WELGENE, LB001-02) and fixed with 4% paraformaldehyde (Biosesang, PC2031-100) for 15 min at room temperature.
Ubiquitin Proteomics:Article Title: Deciphering melanophagy: role of the PTK2-ITCH-MLANA-OPTN cascade on melanophagy in melanocytes
Article Snippet: After 24 h, the cells were homogenized and pulled down with anti-MYC-agarose (Santa Cruz Biotechnology, SC-40 AC) via the same methods with immunoprecipitation section. .. Purified MYC or MYC-ITCH were incubated with reaction solution (0.1 μM E1 [Abcam, ab139467], 6.6 μg UBE2L3/UBCH7 [R&D system, E2-640-100], 1.25 μg MLANA protein [Proteintech, Ag13387], 2.5 μM Ub [Abcam, ab139467], 0.02 U/μl inorganic pyrophosphatase solution [ThermoFisher, EF0221], 1 mm dithiothreitol [ThermoFisher, R0861], 0.1 M Mg-ATP [Abcam, ab139467], 5 mm EDTA [GenDEPOT, P3100–001]) at 37°C for 2 h. After incubation, the reaction was terminated with 2X non-reducing gel loading buffer (Abcam, ab139467), and the ubiquitination was analyzed with western blotting. .. B16F1 cells were washed twice with 37°C phosphate-buffered saline (PBS; WELGENE, LB001–02) and fixed with 4% paraformaldehyde (Biosesang, PC2031–100) for 15 min at room temperature.
Article Title: Deciphering melanophagy: role of the PTK2-ITCH-MLANA-OPTN cascade on melanophagy in melanocytes.
Article Snippet: After 24 h, the cells were homogenized and pulled down with anti-MYC-agarose (Santa Cruz Biotechnology, SC-40 AC) via the same methods with immunoprecipitation section. .. Purified MYC or MYC-ITCH were incubated with reaction solution (0.1 μM E1 [Abcam, ab139467], 6.6 μg UBE2L3/UBCH7 [R&D system, E2-640-100], 1.25 μg MLANA protein [Proteintech, Ag13387], 2.5 μM Ub [Abcam, ab139467], 0.02 U/μl inorganic pyrophosphatase solution [ThermoFisher, EF0221], 1 mM dithiothreitol [ThermoFisher, R0861], 0.1 M Mg-ATP [Abcam, ab139467], 5 mM EDTA [GenDEPOT, P3100-001]) at 37°C for 2 h. After incubation, the reaction was terminated with 2X non-reducing gel loading buffer (Abcam, AC CE PT ED M AN US CR IP T ab139467), and the ubiquitination was analyzed with western blotting. .. B16F1 cells were washed twice with 37°C phosphate-buffered saline (PBS; WELGENE, LB001-02) and fixed with 4% paraformaldehyde (Biosesang, PC2031-100) for 15 min at room temperature.
Western Blot:Article Title: Deciphering melanophagy: role of the PTK2-ITCH-MLANA-OPTN cascade on melanophagy in melanocytes
Article Snippet: After 24 h, the cells were homogenized and pulled down with anti-MYC-agarose (Santa Cruz Biotechnology, SC-40 AC) via the same methods with immunoprecipitation section. .. Purified MYC or MYC-ITCH were incubated with reaction solution (0.1 μM E1 [Abcam, ab139467], 6.6 μg UBE2L3/UBCH7 [R&D system, E2-640-100], 1.25 μg MLANA protein [Proteintech, Ag13387], 2.5 μM Ub [Abcam, ab139467], 0.02 U/μl inorganic pyrophosphatase solution [ThermoFisher, EF0221], 1 mm dithiothreitol [ThermoFisher, R0861], 0.1 M Mg-ATP [Abcam, ab139467], 5 mm EDTA [GenDEPOT, P3100–001]) at 37°C for 2 h. After incubation, the reaction was terminated with 2X non-reducing gel loading buffer (Abcam, ab139467), and the ubiquitination was analyzed with western blotting. .. B16F1 cells were washed twice with 37°C phosphate-buffered saline (PBS; WELGENE, LB001–02) and fixed with 4% paraformaldehyde (Biosesang, PC2031–100) for 15 min at room temperature.
Article Title: Deciphering melanophagy: role of the PTK2-ITCH-MLANA-OPTN cascade on melanophagy in melanocytes.
Article Snippet: After 24 h, the cells were homogenized and pulled down with anti-MYC-agarose (Santa Cruz Biotechnology, SC-40 AC) via the same methods with immunoprecipitation section. .. Purified MYC or MYC-ITCH were incubated with reaction solution (0.1 μM E1 [Abcam, ab139467], 6.6 μg UBE2L3/UBCH7 [R&D system, E2-640-100], 1.25 μg MLANA protein [Proteintech, Ag13387], 2.5 μM Ub [Abcam, ab139467], 0.02 U/μl inorganic pyrophosphatase solution [ThermoFisher, EF0221], 1 mM dithiothreitol [ThermoFisher, R0861], 0.1 M Mg-ATP [Abcam, ab139467], 5 mM EDTA [GenDEPOT, P3100-001]) at 37°C for 2 h. After incubation, the reaction was terminated with 2X non-reducing gel loading buffer (Abcam, AC CE PT ED M AN US CR IP T ab139467), and the ubiquitination was analyzed with western blotting. .. B16F1 cells were washed twice with 37°C phosphate-buffered saline (PBS; WELGENE, LB001-02) and fixed with 4% paraformaldehyde (Biosesang, PC2031-100) for 15 min at room temperature.
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