The MOST ROUTINELY USED pipetted in the molecular laboratory.
Automatic pipette
They used to measure and transfer volumes of liquid accurately (microscale).
Automatic pipette
When aspirating and dispensing fluids, maintain angles closest to vertical. Angles GREATER THAN 20° of vertical will affect results.
Angles
When aspirating fluids, only immerse, the tip as LITTEL AS POSSIBLE, while making sure to completely aspirate the full volume.
Immersion
Remove adhering liquid by brushing the tip against the rim of the primary vessel.
Wipe
For AQUEOUS SOLUTIONS, radioactive compounds, acid/alkalis, and nucleotide solutions; which may require MIXING following dispensing. Forms FOAMS and BUBBLES.
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Forward pipetting
For precise pipetting of SMALL VOLUMES, pipetting of highly VISCOUS or VOLATILE compounds, and solutions that TEND TO FOAM or splash.
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Reverse pipetting
For precise repetitive pipetting of the SAME VOLUME in which carry over is not concern.
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Repetitive pipetting
For dispensing full amounts of HETEROGENOUS SAMPLES such as whole blood and serum.
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Pipetting of Heterogenous Samples
Neutralizes capillary effect and equilibrates the temperature between the air cushion, pipet tip, and the liquid itself.
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Pre-wetting