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SOLVED: You are given 10X protein gel running buffer (Tris/Glycine SDS). Make 800 mL for electrophoresis of your samples on SDS-PAGE gel.You have 10 μL of protein samples to analyze for induced bacteria. You need to boil samples and perform SDS-PAGE. You have 3X Laemmli buffer. Show how you would process samples for the loading.BONUS: IPTG is an inducer. One can also use it. The advantage of using IPTG is that...By what general methodology were the bacterial cells lysed after induction? What ot
SOLVED: You are given 10X protein gel running buffer (Tris/Glycine S…
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