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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

Code UNSPSC :
41103037

Matériaux

cap (push fit)
conical bottom
polypropylene
polypropylene cap

Stérilité

non-sterile

Caractéristiques

DNase free
PCR clean
RCF 20,000 × g
RNase free
graduations

Conditionnement

pkg of 250 ea (5 x 50ea)

Fabricant/nom de marque

Eppendorf® 022431048

Capacité

2.0 mL

Diamètre

10.5 mm

Couleur

clear

Adéquation

suitable for PCR

Type de liaison

low binding surface

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Catégories apparentées

Description générale

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

Caractéristiques et avantages

Signifcantly reduce sample-to-surface binding to ensure maximal recovery of DNA and RNA molecules

Informations légales

Eppendorf is a registered trademark of Eppendorf AG
Eppendorf LoBind is a registered trademark of Eppendorf AG

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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

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
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
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
M Yang et al.
International journal of pharmaceutics, 331(2), 176-181 (2006-11-28)
Salmon calcitonin (sCT) powders suitable for inhalation, containing chitosan and mannitol as absorption enhancer and protection agent, respectively, were prepared using a spray-drying process. The effect of chitosan on physicochemical stability of sCT in the dry powder was investigated by
Hartmut Stocker et al.
Antimicrobial agents and chemotherapy, 50(2), 667-673 (2006-01-27)
Therapeutic drug monitoring (TDM) is gaining importance for improving the success of antiretroviral treatment in human immunodeficiency virus-infected patients. However, enfuvirtide (ENF) concentrations are not regularly determined. The objective of this work was to study the pharmacokinetics (PK) of ENF
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