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Merck
CN

EP951040601

Eppendorf® Protein LoBind Microplate 384/V-PP

PCR clean, V-bottom clear wells, white border, pack of 240 ea (10 bags × 24 plates)

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UNSPSC代码:
41106300
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物料

V-bottom clear wells
polypropylene

无菌性

non-sterile

特点

PCR clean
lid: no
skirt

包装

pack of 240 ea (10 bags × 24 plates)

制造商/商品名称

Eppendorf® 951040601

尺寸

384 well

孔体积

140 μL

颜色

clear wells
white border

适用性

suitable for (protein analysis)
suitable for PCR

一般描述

Microplate 384/V-PP, Protein LoBind, wells clear, 140 µL, PCR clean, white, 240 plates (10 bags × 24 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

特点和优势

  • 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

法律信息

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

法规信息

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分析证书(COA)

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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
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
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
Byung-Gyu Kim et al.
Proteomics, 6(4), 1166-1174 (2006-01-20)
Runx2 is a key transcription factor in osteoblast differentiation, and its activity is regulated by fibroblast growth factors (FGFs). Craniosynostosis, characterized by premature suture closure, results from mutations that generate constitutively active FGF receptors (FGFRs). We previously showed that FGF/FGFR-activated

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