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By inoculating a single colony into 10 mL 2× YT media containing ampicillin (100 μg/mL) and glucose (2.0%) overnight at 37 °C, with shaking at 160 rpm. The overnight cultures were used to inoculate 10 mL fresh 2× YT media (HeV NFL) or Terrific Broth (HeV NCORE) containing ampicillin (100 μg/mL) and glucose (0.1%) at a starting OD600nm of 0.1 and the culture was grown at 37 °C, 160 rpm, until an OD600nm of 0.5 was reached, at which point the temperature was reduced to 26 °C for HeV NFL and 18 °C for HeV NCORE. At an OD600nm of 0.8, the expression of both HeV N constructs was induced by the addition of 1.0 mM isopropyl-β-d-thiogalactopyranoside (IPTG, GoldBio) and 0.25% arabinose (Sigma–Aldrich) and protein expression monitored over a 20 h period by the collection of 200 μL culture aliquots at T = 0, 4, and 20 h post-induction. |
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Protocol tips |
By inoculating a single colony into 10 mL 2× YT media containing ampicillin (100 μg/mL) and glucose (2.0%) overnight at 37 °C, with shaking at 160 rpm. The overnight cultures were used to inoculate 10 mL fresh 2× YT media (HeV NFL) or Terrific Broth (HeV NCORE) containing ampicillin (100 μg/mL) and glucose (0.1%) at a starting OD600nm of 0.1 and the culture was grown at 37 °C, 160 rpm, until an OD600nm of 0.5 was reached, at which point the temperature was reduced to 26 °C for HeV NFL and 18 °C for HeV NCORE. At an OD600nm of 0.8, the expression of both HeV N constructs was induced by the addition of 1.0 mM isopropyl-β-d-thiogalactopyranoside (IPTG, GoldBio) and 0.25% arabinose (Sigma–Aldrich) and protein expression monitored over a 20 h period by the collection of 200 μL culture aliquots at T = 0, 4, and 20 h post-induction. |
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