A tube with water how to say if it is having protein
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normally protein induction is done with an OD600 between 0.5 - 1.0. The cells should be in the logarithmic phase. Induction time varies between 2h up to over night or even loger. Normally 3h are a good starting point. Grow your cells until they have reached OD ~0.7 and induce with 1mM IPTG. Take an aliquot for SDS-PAGE after 1h, 2h, 3h and 4hrs and analysis. This will give you a good starting point for your protein synthesis. When starting testing clones it is always good to start with a fresh strike out or fresh transformation and test several clones. Sometime you can see differences between your clones even when all shoul be identical
Here is the answer
normally protein induction is done with an OD600 between 0.5 - 1.0. The cells should be in the logarithmic phase. Induction time varies between 2h up to over night or even loger. Normally 3h are a good starting point. Grow your cells until they have reached OD ~0.7 and induce with 1mM IPTG. Take an aliquot for SDS-PAGE after 1h, 2h, 3h and 4hrs and analysis. This will give you a good starting point for your protein synthesis. When starting testing clones it is always good to start with a fresh strike out or fresh transformation and test several clones. Sometime you can see differences between your clones even when all shoul be identical
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normally protein induction is done with an OD600 between 0.5 - 1.0. The cells should be in the logarithmic phase. Induction time varies between 2h up to over night or even loger. Normally 3h are a good starting point. Grow your cells until they have reached OD ~0.7 and induce with 1mM IPTG. Take an aliquot for SDS-PAGE after 1h, 2h, 3h and 4hrs and analysis. This will give you a good starting point for your protein synthesis. When starting testing clones it is always good to start with a fresh strike out or fresh transformation and test several clones. Sometime you can see differences between your clones even when all shoul be identical
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