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Briefly, cells were washed twice in phosphate-buffered saline (PBS) and cell pellets were lysed in electrophoresis buffer and boiled for 10 min.
All reactions were stopped by adding 5 × SDS loading buffer and boiled for 10 min at 95 °C for WB analysis21.
The total of 30 μg/mL of cell lysates were resuspended in Laemmli loading loading buffer, and boiled for 10 min at 95 °C.
The precipitates were mixed with 5× western blot loading buffer and boiled for 5 min.
1011 phage particles were mixed in Laemmli buffer and boiled for 5 min.
Whole cell lysates were suspended in lamaelli buffer and boiled for 15 minutes, followed by centrifugation.
Powder was transferred to boiling SDS-sample buffer and boiled for 5 minutes.
Precipitated proteins were eluted with 2× SDS-PAGE sample buffer and boiled for 10 minutes.
Immunoprecipitates were washed thoroughly prior to resuspension in 2x Laemmli sample buffer and boiled for 3 minutes.
Two volume of protein samples were mixed with one volume of 3× Laemmli buffer and boiled for five minutes.
The total cell lysates were mixed with 5× Laemmli buffer and boiled for 5 min at 100°C.
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CEO of Professional Science Editing for Scientists @ prosciediting.com