material
clear wells, colorless wells, polypropylene , white plate
sterility
non-sterile
feature
lid: no
packaging
pkg of 40 ea (5 bags × 8 plates)
manufacturer/tradename
Eppendorf® 951032000
capacity
500 μL
size
96 wells
well volume
500 μL
color
white border
suitability
suitable for PCR, suitable for molecular biology
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General description
Deepwell Plate 96/500µL, DNA LoBind, wells clear, 500 µL, LoBind, PCR clean, white, 40 plates (5 bags × 8 plates)
- 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
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 SE
OptiTrack is a registered trademark of Eppendorf SE
RecoverMax is a registered trademark of Eppendorf SE
法规信息
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Kelly Hodge et al.
Journal of proteomics, 88, 92-103 (2013-03-19)
Mass spectrometry, in the past five years, has increased in speed, accuracy and use. With the ability of the mass spectrometers to identify increasing numbers of proteins the identification of undesirable peptides (those not from the protein sample) has also
Arzu Umar et al.
Proteomics, 7(2), 323-329 (2006-12-14)
Proteomics assays hold great promise for unraveling molecular events that underlie human diseases. Effective analysis of clinical samples is essential, but this task is considerably complicated by tissue heterogeneity. Laser capture microdissection (LCM) can be used to selectively isolate target
Cláudia P Grou et al.
The Journal of biological chemistry, 283(21), 14190-14197 (2008-03-25)
According to current models of peroxisomal biogenesis, newly synthesized peroxisomal matrix proteins are transported into the organelle by Pex5p. Pex5p recognizes these proteins in the cytosol, mediates their membrane translocation, and is exported back into the cytosol in an ATP-dependent
Steven J Bark et al.
Journal of proteome research, 6(11), 4511-4516 (2007-09-14)
Differential recovery of peptides due to nonspecific adsorption can seriously compromise reproducibility and quality of proteomic data for peptide analyses by liquid chromatography-mass spectrometry (LC-MS). This study demonstrates large variations in reproducibility and quantitation of LC-MS data for peptides derived
Hongchang Qu et al.
Immunobiology, 218(4), 496-505 (2012-07-17)
Therapeutic modulation of the complement system has become increasingly important in line with the growing recognition of the role of complement in numerous diseases. Compstatin, a peptidic inhibitor that acts at the central level of the complement cascade, is currently
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