EP022431048
Eppendorf® DNA LoBind tubes
capacity 2.0 mL, PCR clean, pkg of 250 ea (5 x 50ea)
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About This Item
Código UNSPSC:
41103037
Preço e disponibilidade não estão disponíveis no momento.
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Materiais
cap (push fit)
conical bottom
polypropylene
polypropylene cap
esterilidade
non-sterile
Características
DNase free
PCR clean
RCF 20,000 × g
RNase free
graduations
embalagem
pkg of 250 ea (5 x 50ea)
fabricante/nome comercial
Eppendorf® 022431048
capacidade
2.0 mL
Diâmetro
10.5 mm
cor
clear
adequação
suitable for PCR
tipo de ligação
low binding surface
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Descrição geral
Eppendorf LoBind® tubes, snap cap, 2.0 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
Maximize nucleic acid recovery. Eppendorf LoBind Tubes signifcantly reduce sample-to-surface binding to ensure maximal recovery of DNA and RNA molecules. The ideal solution for sample preparation and long-term storage of your precious nucleic acids
Características e benefícios
Signifcantly reduce sample-to-surface binding to ensure maximal recovery of DNA and RNA molecules
Informações legais
Eppendorf is a registered trademark of Eppendorf AG
Eppendorf LoBind is a registered trademark of Eppendorf AG
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Certificados de análise (COA)
Lot/Batch Number
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M Yang et al.
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E I Trilisky et al.
Journal of chromatography. A, 1142(1), 2-12 (2007-01-24)
Purified viruses are used in gene therapy and vaccine production. Ion-exchange chromatography (IEC) is the most common method for large-scale downstream purification of viruses and proteins. Published IEC protocols provide details for specific separations but not general methods for selecting
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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Antimicrobial agents and chemotherapy, 50(2), 667-673 (2006-01-27)
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Nikos Tsolakos et al.
Vaccine, 28(18), 3211-3218 (2010-03-02)
In this study, we evaluated the effect of the growth medium on the composition and immunogenicity of meningococcal outer membrane vesicle (OMV) vaccines after cultivation of the Norwegian serogroup B 44/76 vaccine strain in either Frantz' or modified Catlin-6 media
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