Common mistakes when pipetting | Abyntek Biopharma (2024)

Pipettes are essential instruments for accurately measuring and dispensing reagents. But that precision is of little use if the measurements are not made exactly. Certain common mistakes when pipetting can directly affect that accuracy and hamper the reproducibility of the assays.

In this post, we tell you what are those common mistakes when pipetting and how we can avoid them.

At Abyntek Biopharma we are experts in reagents for scientific research. If you have questions about how to carry out your experiment, ask our experts to advise you throughout the process.

Mistake #1: not assessing the viscosity of the sample

It is important to note the physical properties of the sample, as these directly affect the volume dispensed. In the case of dense samples containing large and viscous molecules, they tend to stick to the tip surface, dispensing more slowly. In contrast, samples containing ethanol, for example, being less viscous and more volatile, will be dispensed more quickly and will tend to evaporate.

Some of the ways to minimize these effects are through the use of ultra-low retention pipet-tips, which contain a hydrophobic plastic additive that prevents liquid from sticking to the inside of the tip, or through reverse pipetting.

Common mistakes when pipetting | Abyntek Biopharma (1)

Mistake #2: DISPENSING LIQUID REAGENTS TOO FAST

Pipetting too quickly increases the probability of making mistakes in dispensing the correct volumes, as well as favouring contamination of the pipettes, among other things.

MISTAKE #3: PIPETTING DIFFERENT SAMPLES WITH THE SAME TIP

If the same tip is used to extract and dispense a sample and then immediately pipet another sample without changing it, sample contamination may be induced.

MISTAKE #4: failing to perform proper pipette maintenance

Pipettes can lead to error in measuring volumes or cause contamination if not maintained correctly.

Daily cleaning with 70% ethanol is essential, as well as the use of different pipettes for general tests and for more specific tests such as those that require RNAse-free environments.

MISTAKE #5: NOT CALIBRATING THE PIPETTES WITHIN THE ESTABLISHED DEADLINES

It is recommended to calibrate the pipettes at least once a year, an ideally every 3 months, to ensure that the measurements made with them are accurate.

MISTAKE #6: PIPETTING FROM THE WRONG ANGLE

The correct angles for pipetting are 90º to aspirate and 45º to dispense.

MISTAKE #7: ASPIRATE AIR

Although it may seem simple, it is a common mistake that must be paid attention to, since in addition to pipetting an inaccurate volume, when aspirating air, the liquid can enter the neck of the pipette.

Mistake #8: EXCESSIVELY immerse the pipette tip when aspirating the sample

The liquid should be aspirated from the surface of the sample, taking care not to aspirate air. For reference, 1-5 ml pipets should be inserted 5-6 mm below the meniscus, while smaller volume pipettes should be inserted only 2-3 mm.

Common mistakes when pipetting | Abyntek Biopharma (2)

MISTAKE #9: STORE PIPETTES IN A HORIZONTAL POSITION

Pipettes should be stored in an upright position, preferably in stands specially designed for them. In this way, liquids that may have entered the neck of the pipette are prevented from escalating and causing contamination and/or corrosion phenomena.

MISTAKE #10: NOT USING THE RIGHT TIPS

Another common mistake when pipetting is to no take into account the size of the tips, that must be adapted to each specific pipette to ensure the precision and accuracy of the measurements, and to avoid contamination. If the tips do not fit correctly, air can scape when you aspirate and dispense the liquid sample, leading to inaccurate results.

MISTAKE #11: NOT MOISTENING THE TIPS PREVIOUSLY

Dipping the tips increases the moisture within the tips, thus minimising solution evaporation. This practice is usually recommended for volumes greater than 10µL.

MISTAKE #12: FAILING TO TAKE INTO ACCOUNT THE ROOM TEMPERATURE AND /OR THE TEMPERATURE OF THE SAMPLE

Pipette calibration is usually done at room temperature, so if you work at significantly lower or higher temperatures, the measurement will not be accurate. Sample temperatures can also cause dispensed volumes to vary.

mistake #13: APplying the pipetting technique incorrectly

The main rules for correct pipetting can be summarized as:

  • Pipetting slowly and gently.
  • Keep the pipette upright when aspirating the sample.
  • Dip tip slightly into sample when aspirating.
  • Dispense the liquid on the side well or on the liquid at 45 º angle.

Do not hesitate to contact us and we will advise you on the reagent that best suits your research.

Common mistakes when pipetting | Abyntek Biopharma (2024)

FAQs

What are the common errors when pipetting solutions? ›

Common mistakes when pipetting and how to avoid them
  • Mistake #1: not assessing the viscosity of the sample. ...
  • Mistake #2: DISPENSING LIQUID REAGENTS TOO FAST. ...
  • MISTAKE #3: PIPETTING DIFFERENT SAMPLES WITH THE SAME TIP. ...
  • MISTAKE #4: failing to perform proper pipette maintenance.
Feb 1, 2023

What are three possible sources of error in the use of a pipette? ›

Sources of Error in Pipetting
  • Failure of properly align the meniscus with the volume mark.
  • Parallax error: Your eye must be level with the volume mark and the pipet vertical. ...
  • Forcing the solution out of the pipet causes too much to be delivered.

What common errors in handling a micropipettor can account for pipetting too much reagent into a tube? ›

What are the common errors in handling a micropipette could result in pippeting volumes greater than the desired volume? Pushing past the 1st stop. letting go of the button too quickly when drawing from a solution not expelling all of the liquid from a previous draw.

What are random errors when using a pipette? ›

Some Random errors while using Pipettes are : Not properly aligning the meniscus with the volume mark. Forcing the solution out of the pipette causes too much solution to be delivered. Using pipette with broken tip.

What are the three rules of pipetting? ›

The following rules apply to all types of pipettes. Never put a pipette in your mouth. Draw the liquid into the pipette using a rubber bulb or pipette pump. Never withdraw a liquid from a near-empty container.

How to minimize pipetting error? ›

These tips can help you reduce pipetting errors during experiments:
  1. Push down to attach the tip securely, but don't push so hard that you bend or warp the tip.
  2. Pre-wet the pipette tip by taking up some liquid and releasing it.
  3. Don't rush.

What is the largest source of pipetting problems? ›

One common source of error is using an incorrect pipette (or tips) for your liquid sample. Our article on piston pipettes provides some excellent insight on how to reduce this source of pipetting error. Another source of pipetting error that is often encountered is working with pipettes that are not ergonomic.

What can affect the accuracy of a pipette? ›

Temperature has many effects on pipetting accuracy. The factor that has the greatest effect is the temperature difference between the delivery device and the liquid. The air gap (dead air volume) between the liquid surface and the piston experiences thermal expansion effects unique to the case.

What are the two most important factors to consider during pipetting? ›

Factors affecting the accuracy of Air Displacement Pipettes:
  • Temperature. The most important factor in pipetting accuracy is the liquid temperature. ...
  • Density. Density is the mass/volume ratio of the liquid. ...
  • Altitude. The geographic altitude affects the accuracy through the air pressure.

Why would a pipette fail calibration? ›

From improper operator technique to fluid viscosity issues, to variable environmental factors and internal pipette component damage, the sources of error are many and the potential for failure is real.

What are two things you should never do when using a micropipette? ›

Never point a pipette up. This may cause liquid to run down into the pipette destroying it. When withdrawing liquids with the pipette, always release the plunger slowly. This prevents liquid from rushing into the end of the pipette and clogging it up.

What is the maximum error of a pipette? ›

Tolerance limits for Digital Pipettes
Pipet RangeVolume (mL or μL)Percent Measurement Error
100–1000 μL100±3.0%
500±1.0%
1000±0.6%
1–10 mL1±3.0%
5 more rows
Aug 15, 2023

What is a parallax error in pipetting? ›

Parallax Errors: Parallax occurs when the operator's eye is not at the same level as the meniscus of the liquid in the pipette, leading to inaccuracies in volume measurement.

How do you know if a pipette is accurate? ›

The most common way to check your pipette accuracy is by weighing water. The density of water is 1 g/mL. This means that every microliter (µL) should weigh exactly 0.001 g using a high-precision balance.

What are common random errors? ›

Some common sources of random error include: natural variations in real world or experimental contexts. imprecise or unreliable measurement instruments. individual differences between participants or units. poorly controlled experimental procedures.

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