Eppendorf™ epT.I.P.S.™ 384 Reloads, Eppendorf Quality™,

epT.I.P.S. 384 micropipette tips with innovative SOFTattach technology are optimally coordinated to Eppendorf 16 and 24-channel pipettes Research plus and Xplorer plus. Process 384-well plates manually with highest level of tip tightness and coaxiality but extraordinary low operating forces.

Catalog Number	Mfr. No.	Volume (Metric)	Packaging
05-413-608	Eppendorf™ 0030076044	20 to 0.1 μL	10 trays × 384 tips
05-413-611	Eppendorf™ 0030076052	100 to 0.5 μL	10 trays × 384 tips
05-413-609	Eppendorf™ 0030076028	20 to 0.1 μL	5 trays × 384 tips

Description

• Designed for a cone distance of 4.5 mm
• epT.I.P.S. 384 pipette tips build a system together with the Research plus and Xplorer plus 16 and 24-channel pipettes for utmost safety and reliability
• 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 reduced by SOFTattach for ergonomic working conditions

Specifications

• Autoclavable: Autoclavable
• Color: Clear
• Filtered: Non-filtered
• Material: Polypropylene
• Sterility: Sterile
• Tip Style: Universal

• Clean Claims: Biopur™, Eppendorf Quality™, PCR clean, Sterile
• Disposable: Yes
• Format: Refill
• Packaging: 10 trays × 384 tips
• Storage Requirements: Room temperature

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.