추천 제품
설명
for PCR Purification with Polymerase Removal
저장 온도
room temp
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일반 설명
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.
애플리케이션
Diffinity RapidTip®2 has been used to purify PCR products.
특징 및 장점
- Single step
- Recovers 90% of high quality dsDNA
- Removes polymerase from PCR reactions and cloning
- Optimized for 50 μL reaction
법적 정보
RADIANT is a registered trademark of Bio-Rad Laboratories, Inc.
RapidTip is a registered trademark of Diffinity Genomics, Inc.
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Assessment of cecal microbiota, integron occurrence, fermentation responses, and Salmonella frequency in conventionally raised broilers fed a commercial yeast-based prebiotic compound.
Lee SI
Poultry Science, 95(1), 144-153 (2016)
HLA-G 3'UTR Polymorphisms Impact the Prognosis of Stage II-III CRC Patients in Fluoropyrimidine-Based Treatment.
Garziera M
PLoS ONE, 10(12), e0144000-e0144000 (2015)
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
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