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
colorless wells
conical bottom
polypropylene
yellow plate
capacity:
500 μL
well volume:
500 μL
sterility:
non-sterile
binding type:
low binding surface
feature:
lid: no
Recommended Products
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
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
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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
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
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
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
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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