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Merck
CN

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

96 wells

binding type

low binding surface

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

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

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Rebecca F Turcotte et al.
Biochemical and biophysical research communications, 377(2), 512-514 (2008-10-22)
One of the tightest known protein-protein interactions in biology is that between members of the ribonuclease A superfamily and the ribonuclease inhibitor protein (RI). Some members of this superfamily are able to kill cancer cells, and the ability to evade
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
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
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
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

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