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
UNSPSC Code:
41106300
material:
clear wells
colorless wells
conical bottom
polypropylene
yellow plate
colorless wells
conical bottom
polypropylene
yellow plate
size:
96 well
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 20 ea (5 bags × 4 plates)
manufacturer/tradename
Eppendorf® 951032921
capacity
500 μL
size
96 well
well volume
1000 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 96/1000 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
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
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
M Yang et al.
International journal of pharmaceutics, 331(2), 176-181 (2006-11-28)
Salmon calcitonin (sCT) powders suitable for inhalation, containing chitosan and mannitol as absorption enhancer and protection agent, respectively, were prepared using a spray-drying process. The effect of chitosan on physicochemical stability of sCT in the dry powder was investigated by
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
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