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Key Documents

EP951032921

Eppendorf® Deepwell plates, Protein LoBind, 96 wells

yellow plate, conical bottom, colorless wells, capacity 500 μL, pkg of 20 ea (5 bags × 4 plates)

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About This Item

Code UNSPSC :
41106300

Matériaux

clear wells
colorless wells
conical bottom
polypropylene
yellow plate

Stérilité

non-sterile

Caractéristiques

lid: no

Conditionnement

pkg of 20 ea (5 bags × 4 plates)

Fabricant/nom de marque

Eppendorf® 951032921

Capacité

500 μL

Volume des puits

1000 μL

Couleur

yellow border

Adéquation

suitable for (protein analysis)
suitable for PCR

Type de liaison

low binding surface

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Catégories apparentées

Description générale

Deepwell Plate 96/1000 µL, Protein LoBind, wells colorless, 1,000 µL, PCR clean, yellow, 20 plates (5 bags × 4 plates)
  • Eppendorf LoBind material ensures excellent sample recovery for improved assay results
  • Free of surface coating (e.g., silicone) to minimize the risk of sample interference
  • Lot-certified PCR clean purity grade: free of human DNA, DNase, RNase and PCR inhibitors
  • Available in tube, microplate, and deepwell plate formats for easy-up scaling
  • Unique OptiTrack® matrix: 30 % faster sample identification and fewer pipetting errors
  • RecoverMax well design: optimized well geometry for minimal remaining/dead volume and excellent mixing properties
  • Raised well rims and a smooth surface ensure reliable sealing in plates

Caractéristiques et avantages

  • Eppendorf LoBind material ensures optimized sample recovery for improved assay results
  • Free of surface coating (e.g. silicone) to minimize the risk of sample interference
  • Lot-certified PCR clean purity grade: free of human DNA, DNase, RNase and PCR inhibitors
  • Available in tube, microplate, and deepwell plate formats for easy-up scaling
  • High-contrast Unique OptiTrack® matrix: up to 30 % faster sample identification and fewer pipetting errors
  • RecoverMax® well design: optimized well geometry for minimal remaining/dead volume and excellent mixing properties
  • Raised well rims and a smooth surface ensure reliable sealing

Informations légales

Eppendorf is a registered trademark of Eppendorf AG
OptiTrack is a registered trademark of Eppendorf AG
RecoverMax is a registered trademark of Eppendorf AG

Certificats d'analyse (COA)

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Nikos Tsolakos et al.
Vaccine, 28(18), 3211-3218 (2010-03-02)
In this study, we evaluated the effect of the growth medium on the composition and immunogenicity of meningococcal outer membrane vesicle (OMV) vaccines after cultivation of the Norwegian serogroup B 44/76 vaccine strain in either Frantz' or modified Catlin-6 media
Sharon N Finger et al.
Nucleic acids research, 36(4), 1260-1272 (2008-01-05)
Telomerase is a ribonucleoprotein enzyme that maintains chromosome ends through de novo addition of telomeric DNA. The ability of telomerase to interact with its DNA substrate at sites outside its catalytic centre ('anchor sites') is important for its unique ability
Thandavarayan Kathiresan et al.
Methods in molecular biology (Clifton, N.J.), 493, 269-286 (2008-10-08)
Functional proteomics comprises a wide range of technologies for the identification of novel protein-protein interactions and biological markers. Studies of protein-protein interactions have gained from the development of techniques and technologies such as immunoprecipitation, preparative two-dimensional (2-D) gel electrophoresis for
Hartmut Stocker et al.
Antimicrobial agents and chemotherapy, 50(2), 667-673 (2006-01-27)
Therapeutic drug monitoring (TDM) is gaining importance for improving the success of antiretroviral treatment in human immunodeficiency virus-infected patients. However, enfuvirtide (ENF) concentrations are not regularly determined. The objective of this work was to study the pharmacokinetics (PK) of ENF
E I Trilisky et al.
Journal of chromatography. A, 1142(1), 2-12 (2007-01-24)
Purified viruses are used in gene therapy and vaccine production. Ion-exchange chromatography (IEC) is the most common method for large-scale downstream purification of viruses and proteins. Published IEC protocols provide details for specific separations but not general methods for selecting
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