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Eppendorf™ epT.I.P.S.™ 384 Reloads - Micropipette Tips
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.
Supplier: Eppendorf™ 0030076044
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
Specifications
| 0.1 to 20 μL | |
| Non-sterile | |
| Autoclavable | |
| 1.7 in. | |
| Eppendorf Quality (Non-sterile) | |
| Universal | |
| Universal | |
| 3840 Tips | |
| Light Pink | |
| Air-cushion System | |
| Polypropylene |
| Non-filtered | |
| Colorless | |
| epT.I.P.S.™ 384 Reloads | |
| 42 mm | |
| Room temperature | |
| Refill | |
| 3,840 Tips (10 Trays x 384 Tips) | |
| Micropipette Tips | |
| Single-use | |
| epT.I.P.S. |
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.