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一般描述
Diffinity RapidTip2 effectively removes dNTPs, primers and primer dimers while providing greater than 90% recovery of pure DNA fragments from 100 bp to 10 kb. The functional pipette tip contains everything you need for PCR purification with polymerase removal. The tip is filled with a proprietary adsorption technology that has a differential affinity for PCR components. The impurities (polymerase, single strand primers, and nucleotides) are removed from the solution as it enters the tip. The RapidTip2 is optimized for a 50 μL PCR reaction sample, and the dispensed solution yields purified, high quality DNA ready for downstream applications such as DNA sequencing, SNP analysis, microarray printing, and T-A cloning.
Diffinity RapidTip2 effectively removes dNTPs, primers, primer dimers and DNA polymerase while providing greater than 90% recovery of pure DNA fragments from 100 bp to 10 kb. The functional pipette tip contains everything you need for PCR purification with polymerase removal. The tip is filled with a proprietary adsorption technology that has a differential affinity for PCR components. The dispensed solution yields purified, high quality DNA ready for downstream applications such as DNA sequencing, SNP analysis, microarray printing, and T-A cloning.
特点和优势
- Single step
- Recovers 90% of high quality dsDNA
- Removes polymerase from PCR reactions and cloning
- Optimized for 50 μL reaction
法律信息
LTS is a registered trademark of Rainin Instrument, LLC
RapidTip is a registered trademark of Diffinity Genomics, Inc.
Sarah L Dean et al.
Molecular ecology, 23(6), 1364-1378 (2013-10-12)
Nitrogen (N) deposition rates are increasing globally due to anthropogenic activities. Plant community responses to N are often attributed to altered competitive interactions between plants, but may also be a result of microbial responses to N, particularly root-associated fungi (RAF)
H Kühlwein et al.
Journal of applied microbiology, 115(5), 1091-1106 (2013-07-31)
To assess the effects of dietary Saccharomyces cerevisiae β-(1,3)(1,6)-D-glucan supplementation (MacroGard(®)) on mirror carp (Cyprinus carpio L.) intestinal microbiota and ultrastructure of the enterocyte apical brush border. Carp were fed either a control diet or diets supplemented with 0.1, 1
Michael J Goblirsch et al.
PloS one, 8(7), e69831-e69831 (2013-07-31)
A major hindrance to the study of honey bee pathogens or the effects of pesticides and nutritional deficiencies is the lack of controlled in vitro culture systems comprised of honey bee cells. Such systems are important to determine the impact
Teruaki Nakatsuji et al.
Nature communications, 4, 1431-1431 (2013-02-07)
Commensal microbes on the skin surface influence the behaviour of cells below the epidermis. We hypothesized that bacteria or their products exist below the surface epithelium and thus permit physical interaction between microbes and dermal cells. Here to test this
C N Roterman et al.
Proceedings. Biological sciences, 280(1764), 20130718-20130718 (2013-06-21)
The phylogeny of the superfamily Chirostyloidea (Decapoda: Anomura) has been poorly understood owing to limited taxon sampling and discordance between different genes. We present a nine-gene dataset across 15 chirostyloids, including all known yeti crabs (Kiwaidae), to improve the resolution
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