These instruments have been developed in recent years and have been valuable in manipulating tiny volumes, particularly of solutions of DNA and enzymes used in genetic engineering. They function by drawing fluid into the pipet tip using a thumb-driven piston whose movement is calibrated to draw up a specified volume of liquid. The units of volume are in microliters (µL), also termed lambdas ( l). Since there are a million µLs in a liter, 0.1 mL is 100 µL. The plastic disposable tip is discarded after a single use. The tips are color coded according to their capacity: white for 10 µL, yellow for up to 200 µL, and blue for up to 1000 µL.
The advantage of single-use disposable tips in genetic engineering is that there is no possibility of contamination with endonucleases which would destroy DNA samples. Also, the tips are much less expensive than single-use pipettes. However, the instruments are very expensive (about $200 each), and must be handled and cared for properly. NEVER allow fluid up into the body of the pipetter.
Illustrate a displacement pipette and include
all of the following features:
| body thumb plunger calibrated stop blow out stop lock ring volume of aliquot (in window) |
capacity range indication thumb knob (to adjust volume) shaft tip tip ejector button ejection ring |
USE OF THE DISPLACEMENT PIPETTER
1. Select the pipetter whose range
is appropriate for the volume you wish to measure out.
2. Set the volume as follows:
a.
Loosen the lock ring at the base of the thumb plunger.
b
Rotate the thumb knob until the desired
number of µL appears in the window
. [Do not go above the specified range of
the pipetter or you may damage the instrument.]
c.
Snug the lock ring. (Do not over-tighten.)
3. Attach a fresh tip to the pipetter:
a:
Open the box of sterile tips.
b:
Press the pipetter firmly down onto one of the tips, tap once or twice to
firm the fitting.
c:
Pull out the attached tip, immediately close the box to maintain sterility.
4. Draw up the desired volume of fluid:
a:
Before you insert the tip into the sample solution, gently depress
the plunger to the first (calibrated) stop and hold in
place. DO NOT GO PAST THE CALIBRATED STOP.
b:
Insert the pipetter into the sample solution so that the tip is about 3 mm
below the surface.
c:
Allow the plunger to slowly and smoothly return to its original position.
Note that fluid is drawn up into the tip (no
bubbles). DO NOT LET FLUID ENTER PIPETTER BODY.
d:
Withdraw the pipetter from the sample vessel, flame and re-cap vessel to maintain
sterility.
STOPS OF THE THUMB PLUNGER
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5. Deliver the fluid into the receiving
vessel:
a:
Insert the pipet into the receiving vessel so that the tip a: is 3 mm below
the surface of the receiving fluid, or b: touches
the bottom of the empty vessel.
b:
Depress the plunger slowly and smoothly until the first stop is felt.
c:
Press more firmly on the thumb plunger to blow out the remainder of fluid.
You should see a bubble expelled.
KEEP THE PLUNGER HELD DOWN.
d:
Withdraw the pipetter from the vessel, dragging it along the side to leave
any adhered fluid.
e:
Allow the plunger to return to its normal position.
6. Discard the used tip (unless you are
to deliver additional aliquots of the same fluid):
a:
Hold the pipetter over a discard vessel.
b:
Depress the tip eject button with the thumb until the tip is ejected.
PRACTICE USING THE PIPETTER'S FEATURES
Per desk for practice by two students:
2 20-200 uL pipetters
2+ non-sterile tips in a
tray
test tube rack with:
2
13 × 100 mm test tubes, half full of water
4
13 × 100 mm test tubes, empty