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Volumn 217, Issue 1, 2002, Pages 89-94

PCR performance of the highly thermostable proof-reading B-type DNA polymerase from Pyrococcus abyssi

Author keywords

Archaea; DNA polymerase; Polymerase chain reaction; Pyrococcus abyssi

Indexed keywords

AMMONIUM SULFATE; BUFFER; DNA DIRECTED DNA POLYMERASE BETA; HYDROCHLORIC ACID; MAGNESIUM SULFATE; NUCLEOTIDE; PARATHION; PHENFORMIN; POTASSIUM CHLORIDE; RECOMBINANT ENZYME; TAQ POLYMERASE;

EID: 0037137278     PISSN: 03781097     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1097(02)01037-6     Document Type: Article
Times cited : (32)

References (16)
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    • A rapid and sensitive method for the quantitation of microgram quantities of protein using the principle of protein-dye binding
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    • Bradford, M.M.1
  • 14
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    • PCR performance of the B-type DNA polymerase from the thermophilic euryarchaeon Thermococcus aggregans improved by mutations in the Y-GG/A motif
    • Bohlke K., Pisani F.M., Vorgias C.E., Frey B., Sobek H., Rossi M., Antranikian G. PCR performance of the B-type DNA polymerase from the thermophilic euryarchaeon Thermococcus aggregans improved by mutations in the Y-GG/A motif. Nucleic Acids Res. 15:2000;3910-3917.
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    • Fidelity of DNA synthesis by the Thermococcus litoralis DNA polymerase, an extremely heat stable enzyme with proofreading activity
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.