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  7. 16282371

Eppendorf™ epT.I.P.S.™ 384 Reloads - Micropipette Tips
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Eppendorf epT.I.P.S.™ 384 Reloads provide high-precision micropipette tips in 'Eppendorf Quality' and 'PCR clean' grades, tailored for 384-well plate applications, ensuring accuracy, reduced waste, and compatibility in high-throughput labs.

Brand:  Eppendorf™ 0030076010

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Product Code. 16282371

  • 3195.00 DKK / Pack of 3840
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Description

Description

  • epT.I.P.S. 384 pipette tips build a system together with the Research plus and Xplorer plus 16- and 24-channel pipettes as well as 20 μL and 100 μL Move It adjustable tip spacing pipettes for utmost safety and reliability
  • Designed for a cone distance of 4.5 mm
  • Innovative SOFTattach technology allows for reliable tip fit and tightness
  • Fill a whole 384-well plate without loosening pipette tips
  • Perfect tip alignment by extraordinary coaxiality for safe plate maneuvering and liquid transfer
  • The tip shape of the epT.I.P.S. 384 is adjusted to perfectly fit the wells of 384-well plates
  • Tip attachment forces reduced by 40% per cone compared to 8- and 12-channel pipettes
  • Tip ejection forces in 16- and 24-channel pipettes reduced by SOFTeject for ergonomic working conditions
  • Available as reload, and set
  • Available in purity grades of Eppendorf Quality and PCR clean
  • ACT™-labeled by non-profit My Green Lab™ to help you make an informed product choice when it comes to sustainability
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Specifications

Specifications

5 to 100 μL
Non-sterile
Autoclavable
2.1 in.
PCR Clean (Non-sterile)
Universal
Universal
3840 Tips
Light Yellow
Air-cushion System
Polypropylene
Non-filtered
Colorless
epT.I.P.S.™ 384 Reloads
53 mm
Room temperature
Refill
3,840 Tips (10 Trays x 384 Tips)
Micropipette Tips
Single-use
epT.I.P.S.
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The pipette tips of the :Productname: product group with the respective product numbers are designed and constructed for low-contamination transfer of liquids, in particular for samples from the human body and for reagents within the scope of an in-vitro diagnostic application in order to allow the in-vitro diagnostic medical device to be used as intended. The above mentioned :Productname: are in-vitro diagnostic devices according to Directive 98/79/EC of the European Parliament and the Council dated October 27, 1998. They are intended exclusively for single use and for application by qualified staff.