Project Description

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PCRBIO HiFi Polymerase

제품 소개

PCRBIO HiFi Polymerase는 3’→5’ exonuclease (proofreading) activity를 갖고 있어 error rate이 낮아 정확한 PCR 증폭이 가능합니다.
Pfu에 의해 생성된 PCR 산물은 blunt-end form 이므로 일반적으로 TA cloning이 불가능합니다.
GC, AT 비율이 높은 복잡한 template의 증폭에도 효과적이며, 수율을 증가 시키고 cycling 시간을 단축시킬 수 있습니다.


• Taq DNA polymerase 보다 50배 높은 정확도
• Amplification size: < 10 kb
• 3’→5’ exonuclease (proofreading) 활성
• A-tail: No


• High fidelity PCR
• Fast PCR – 35 cycles of 5kb amplicon in under 1.5 hours
• blunt-end cloning
• Site-directed mutagenesis
• Nest generation re-sequencing


• -20℃

Figure 1. Shows amplification of a 5kb amplicon from GAPDH derived from purified human genomic DNA. A 2 fold template dilution series was made from a starting concentration of 100 nanograms of DNA. 25 cycles of 30 seconds denaturation, 30 seconds annealing, and 75 seconds extension were completed in 1 hour. The first row shows PCRBIO HiFi Polymerase, the second row an equivalent product from Finnzymes, and the 3rd-row standard Pfu.

Figure 2. Shows no change in activity is detected in PCRBIO HiFi Polymerase after 28 days at 4˚C, 25˚C and 37˚C.

Figure 3. Shows PCRBIO HiFi Polymerase amplifying a 60% GC 1kb fragment of human GAPDH from genomic DNA. The template is diluted 2 fold over 8 orders of magnitude, starting from 100 nanograms. The first row shows PCRBIO HiFi Polymerase, the second row shows Invitrogens Pfx enzyme, and the 3rd-row Finnzymes Phusion enzyme.


​제품번호 품명 규격 제조사 비교
PB10.41-02 PCRBIO HiFi Polymerase 200 units PCRbiosystems [1 x 0.1ml 2 units/μl] & [3 x 1ml buffer]
PB10.41-10 PCRBIO HiFi Polymerase 1,000 units PCRbiosystems [5 x 0.1ml 2 units/μl] & [15 x 1ml buffer]

관련 논문

PCRBIO HiFi Polymerase

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Gilman, F.R., 2015. Microbial responses and contributions to climate change in Greenland. University of Montana, Missoula, Montana, USA.

Herrmann, B., 2017. Autökologische und molekularbiologische Untersuchungen zur Charakterisierung der Kleidermotte Tineola bisselliella (Lepidoptera) als Referenzorganismus (Doctoral dissertation, Freie Universität Berlin). Supervisors: Dr. Rüdiger Plarre; Prof. Dr. Rupert Mutzel

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Martín Ramírez, R.M., 2014. Estudio de expresión de la familia génica sirtuínas en células de la granulosa humana, y su relación con la calidad oocitaria en técnicas de fecundación in vitro. Universidad de La Laguna, Santa Cruz de Tenerife, Spain.

Pickering, H., 2017. Identification of Chlamydia trachomatis Immune Targets through Immunological and Population-Genomic Screens and Elucidation of Potential Roles in Bacterial Pathogenesis (Doctoral dissertation, London School of Hygiene & Tropical Medicine). Supervisors: Martin Holland; Richard Hayward.

Repin, R.A.M., Mutalib, S.A., Shahimi, S., Khalid, R.M., Ayob, M.K., Bakar, M.F.A. and Isa, M.N.M., 2016, November. Bioinformatics analysis and detection of gelatinase encoded gene in Lysinibacillussphaericus. In AIP Conference Proceedings (Vol. 1784, No. 1, p. 030044). AIP Publishing.

Stankiewicz, E., 2017. Identification of the genetic alterations in prostate cancer metastases (Doctoral dissertation, Queen Mary University of London). Supervisor: Dr Yong-Jie Lu and Prof D. Berney


제품 자료 PCRBIO-HiFi-Polymerase-Product-Flyer.pdf Upload date: 2021.07.02
제품 매뉴얼 PB10.41-PCRBIO-HiFi-Polymerase-Manual.pdf Upload date: 2021.07.02
제품 MSDS PB10.41-PCRBIO-HiFi-Polymerase-MSDS.pdf Upload date: 2021.07.02