Page 26 - An Identity Crisis
P. 26

6. Place the tip of the pipette into the liquid in     2.  Before turning on the power supply, ensure the
                 the tube, but do not touch the bottom. Slowly      supply reads “Volts” and the setting is “Low.”
                 release the plunger to obtain the contents of     3.  Once all lab stations have been checked, turn
                 the tube.
                                                                    on the power supply and twist the knob until
               7.  Carefully suspend the tip in the appropriate     the display reads the voltage suggested by your
                 well in the gel, being careful not to touch the gel   instructor (usually between 60 and 100 volts).
                 itself.
                                                                  4. Within a few minutes the orange dye should be
               8. Press the plunger down slowly to dispense         observed to have moved out of the wells. If the
                 the sample into the well. Do not touch the gel     dye remains in the wells ensure that your power
                 itself. Remove the pipette from the well before    supply is plugged in, is turned on, and is set to
                 releasing the plunger.                             the correct voltage. If problems persist after
                                                                    several minutes more, alert your instructor.
               9. Discard the used tip.
                                                                  5.  As the gel runs, DNA will be visible migrating
             10. Record the location of the sample on your data     through the gel. It will begin as a faint blue
                 collection sheet.
                                                                    streak near the wells.
             11.  Moving from left to right, repeat these steps      6.  After the gel has run for a time, the blue bands will
                 for each sample, using a different well and tip    have separated and grown darker. The blue color
                 each time.
                                                                    will intensify as the DNA stains while the gel runs.
                                                                    The DNA will never become strongly contrasted

             RUNNING THE GEL (45 MIN)                               against the gel, but should be clearly visible.
                                                                  7.  Allow the gel to run until the orange color in the
               1.  Place the lid down on the top of the gel box.    loading dye has migrated about 75% of the way
                 Ensure that the black electrode matches up         through the gel.
                 with the black lead and red with red. Plug the
                 leads into the power supply, also matching the     8. Promptly record the positions of the DNA on the
                 colors.                                            gel on your data collection sheet.


































              26    THE MYSTERY OF LYLE AND LOUISE
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