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D1947

Sigma-Aldrich

Diffinity RapidTip®

for PCR Purification

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Synonym(s):
PCR clean up tip, PCR purification tip, PCR reaction clean-up tip
EC Number:
NACRES:
NA.52

Quality Level

form

solid

manufacturer/tradename

(Diffinity Genomics, Inc.)

capacity

50(µL)

storage temp.

room temp

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This Item
12140314001HPPCRPKROPCR9604
Diffinity RapidTip® for PCR Purification

D1947

Diffinity RapidTip®

High Fidelity PCR Master sufficient for ≤200 reactions, kit of 1 (2 components), suitable for PCR

12140314001

High Fidelity PCR Master

form

solid

form

-

form

-

form

-

capacity

50(µL)

capacity

-

capacity

-

capacity

-

storage temp.

room temp

storage temp.

2-8°C

storage temp.

-

storage temp.

15-25°C

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

-

General description

Diffinity RapidTip 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. 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 and microarray printing.

Application

Diffinity RapidTip® has been used in PCR product purification.

Features and Benefits

  • Single step
  • Recovers 90% of high quality dsDNA
  • Optimized for 25 μL RXN

Legal Information

RapidTip is a registered trademark of Diffinity Genomics, Inc.

pictograms

Health hazard

signalword

Warning

hcodes

Hazard Classifications

STOT RE 2 Inhalation

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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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)
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
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
Parag Vaishampayan et al.
The ISME journal, 7(2), 312-324 (2012-10-12)
The advent of phylogenetic DNA microarrays and high-throughput pyrosequencing technologies has dramatically increased the resolution and accuracy of detection of distinct microbial lineages in mixed microbial assemblages. Despite an expanding array of approaches for detecting microbes in a given sample

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