The objective of this lab was to get a high concentration of virus with a good amount of concentration to isolate the DNA. The materials for this lab are: stands for oakridge tube and high-titer lysate conical tube, 10 milliliters uncontaminated High-Titer lysate, serological pipette, Oakridge tube, 40 microliters of nuclease, incubator, and 4 milliliters of phage buffer. The protocol for lab number 21 is to transfer 10 milliliters uncontaminated High-Titer lysate using serological pipette into the Oakridge tube. Place it into an incubator for half an hour after adding 40 microliters of nuclease, as well as inverting the nucleus and high-titer lysate. After 30 minutes of being inside the incubator, allow the mix to sit for one hour outside the incubator. 4 milliliters of phage buffer is to be added into the nuclease-lysate mixture and gently inverted. Place the mixture in the fridge when
The objective of this lab was to get a high concentration of virus with a good amount of concentration to isolate the DNA. The materials for this lab are: stands for oakridge tube and high-titer lysate conical tube, 10 milliliters uncontaminated High-Titer lysate, serological pipette, Oakridge tube, 40 microliters of nuclease, incubator, and 4 milliliters of phage buffer. The protocol for lab number 21 is to transfer 10 milliliters uncontaminated High-Titer lysate using serological pipette into the Oakridge tube. Place it into an incubator for half an hour after adding 40 microliters of nuclease, as well as inverting the nucleus and high-titer lysate. After 30 minutes of being inside the incubator, allow the mix to sit for one hour outside the incubator. 4 milliliters of phage buffer is to be added into the nuclease-lysate mixture and gently inverted. Place the mixture in the fridge when