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

Catalog No. 05413609
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Volume (Metric):
20 to 0.1 μL

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.

  • 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
TRUSTED_SUSTAINABILITY

Specifications

Volume (Metric) 20 to 0.1 μL
Filtered Non-filtered
Sterility Sterile
Color Clear
Autoclavable Autoclavable
Model epT.I.P.S.™ 384 Set
Length (English) 1.7 in.
Length (Metric) 42 mm
Clean Claims Biopur™, Eppendorf Quality™, PCR clean, Sterile
Storage Requirements Room temperature
Compatibility Universal
Format Hinged Rack
Tip Style Universal
Packaging 5 Trays x 384 Tips
Quantity 1920 Tips
Product Type Micropipette Tips
Color Code White
Disposable Single-use
Product Line epT.I.P.S.
Material Polypropylene
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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.

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