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EP951032123

Eppendorf® Deepwell plates, Protein LoBind, 96 wells

yellow plate, conical bottom, colorless wells, capacity 500 μL, pkg of 40 ea (5 bags × 8 plates)

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About This Item

UNSPSC Code:
41106300
Material:
clear wells
colorless wells
conical bottom
polypropylene
yellow plate
Size:
96 well
Sterility:
non-sterile
Binding type:
low binding surface
Feature:
lid: no
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material

clear wells
colorless wells
conical bottom
polypropylene
yellow plate

sterility

non-sterile

feature

lid: no

packaging

pkg of 40 ea (5 bags × 8 plates)

manufacturer/tradename

Eppendorf® 951032123

capacity

500 μL

size

96 well

well volume

500 μL

color

yellow border

suitability

suitable for (protein analysis)
suitable for PCR

binding type

low binding surface

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General description

Deepwell Plate 96/500 µL, Protein LoBind, wells colorless, 500 µL, PCR clean, yellow, 40 plates (5 bags × 8 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

Features and Benefits

  • 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

Legal Information

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

Regulatory Information

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Dana A N Mustafa et al.
Molecular & cellular proteomics : MCP, 6(7), 1147-1157 (2007-03-16)
The identification of angiogenesis-related proteins is important for the development of new antiangiogenic therapies, and such proteins are potential new biomarkers for gliomas. The aim of this study was to identify proteins that are exclusively present in glioma neovasculature and
Connie Luk et al.
Journal of neurochemistry, 123(3), 396-405 (2012-08-07)
Characteristic tau isoform composition of the insoluble fibrillar tau inclusions define tauopathies, including Alzheimer's disease (AD), progressive supranuclear palsy (PSP) and frontotemporal dementia with parkinsonism linked to chromosome 17/frontotemporal lobar degeneration-tau (FTDP-17/FTLD-tau). Exon 10 splicing mutations in the tau gene
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
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

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