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Diffinity Genomics

RapidTip

DIFFINTIY  RapidTip  for PCR Purification


One minute PCR purification in only a single step !


Features

- Fast, Simple – Recovers clean DNA in a one minute, one step process

- Effective Purification – Removes impurities for downstream applications

- Cost Effective – Requires no capital equipments, extra plastic or liquids

- Environmentally Friendly – Limits waste to the functional pipette tip



Diffinity Genomics has developed an innovative new technology that removes

undesirable impurities from PCR reactions leaving you with nothing but purified

DNA in solution — fast!

DiffinityTM technology effectively removes dNTPs, primers, and primer dimers while providing greater than 80% recovery of pure DNA

fragments ranging in length from 150bp to 10Kb. It dramatically reduces the amount of time to purify and prepare PCR reactions for use

in downstream applications, such as DNA sequencing, SNP analysis, and microarray printing.

The functional pipette tip will fit on most conventional single or multiple, manual or automated laboratory pipettors. Samples containing

DNA and PCR impurities are aspirated into the tip where the impurities are adsorbed onto proprietary surfaces within the tip by mixing

for approximately one minute. Expelling the solution yields purified DNA, the desired product.


Product Comparion Chart

Diffinity RapidTip®

RT025-048
RT025-048L
RT025-096
RT025-096L

Diffinity RapidTip®

RR050-048
RR050-048L
RR050-096
RR050-096L

Impurities removed

dNTP

Yes

Yes

Primer

Yes

Yes

Primer-dimer

Yes

Yes

DNA polymerase

No

Yes

Other Enzymes

No

No

Tip Format

Tip Formats Available

Universal
Rainin LTS®
Robotic  (Contact us)

Universal
Rainin LTS®

Sample Volume

PCR Sample Volume

25 microliters

50 microliters


Fragment Size

Fragment Size Cutoff

Removes < 40bp Retains > 150bp to 10Kb

Removes < 40bp Retains > 150bp to 10Kb

Downstream

Applications

Optimized for these downstream applications

PCR purification prior to Sanger sequencing

PCR purification prior to restriction digestion, TA cloning

PCR purification prior to Sanger sequencing

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