material
cap (push fit), conical bottom, polypropylene , polypropylene cap
sterility
non-sterile
feature
DNase free, PCR clean, RCF 30,000 × g, RNase free, graduations
packaging
pkg of 250 ea (5 x 50ea)
manufacturer/tradename
Eppendorf® 022431021
capacity
1.5 mL
diam.
10.7 mm
color
clear
suitability
suitable for PCR
binding type
low binding surface
General description
最大限度回收核酸。 Eppendorf LoBind 管大幅减少样品与表面吸附，确保最大限度回收 DNA 和 RNA 分子。样品制备和长期储存珍贵核酸的理想解决方案
Eppendorf LoBind® tubes, snap cap, 1.5 mL, PCR clean, colorless, 250 tubes (5 bags × 50 tubes)
- 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
- Precise lid sealing for minimal evaporation rates in tube format
- Rated up to 30,000 x g (25,000 x g for 2.0 mL) centrifugation speed for molecular biology applications
Features and Benefits
大幅减少样品与表面吸附，确保最大限度回收 DNA 和 RNA 分子
Legal Information
Eppendorf LoBind is a registered trademark of Eppendorf SE
Eppendorf is a registered trademark of Eppendorf SE
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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