نتایج جستجو برای: taq polymerase

تعداد نتایج: 128420  

2012
Kush Kumar Nayak Archana Tiwari

The thermostable properties of Taq DNA polymerase from Thermus aquaticus have contributed greatly to the yield, specificity, automation, and utility of the polymerase chain reaction method for amplifying DNA. Taq polymerase is widely used enzyme for DNA amplification in PCR techniques and highly applicable in molecular biology and biotechnology. In this study the Taq gene was amplified from the...

ژورنال: :مجله تازه های بیوتکنولوژی سلولی - مولکولی 0
سمانه گلیج samaneh golayj department of biology, islamic azad university of tonekabon branch, tonekabon, iran.گروه زیست شناسی، دانشگاه آزاد اسلامی واحد تنکابن علی ناظمی ali nazemi department of biology, islamic azad university of tonekabon branch, tonekabon, iran.گروه زیست شناسی، دانشگاه آزاد اسلامی واحد تنکابن مصطفی جعفرپور mostafa jafarpour department of biology, islamic azad university of tonekabon branch, tonekabon, iran.گروه زیست شناسی، دانشگاه آزاد اسلامی واحد تنکابن

سابقه و هدف: آنزیم dna پلیمراز مقاوم به حرارت بعلت کاربرد آن در pcr و تحقیقات بیولوژی مولکولی توجه زیادی را به خود معطوف ساخته است و در نتیجه اهمیت مطالعه روی dna پلیمرازهای مقاوم به حرارت مختلف را دو چندان نموده است. هدف از این مطالعه سنجش عملکرد و میزان تولید آنزیم dna پلیمراز حساس به سرما و مقاوم به حرارت تولید شده در میزبان باکتریایی و خالص سازی سریع و ارزان آن می باشد. مواد و روش ها: بعد ا...

Journal: :Nucleic acids research 1988
M G Peterson

Three DNA polymerases, namely E.coli DNA polymerase 1 (Klenow), reverse transcriptase and T7 DNA polymerase (sequenase), are commonly used for DNA sequencing by the chain termination method of Sanger and colleagues [1). However, the secondary structure of the DNA template can impede the progress of all three polymerases. I have developed a novel procedure in which the thermostable polymerase of...

2009
Rudolph Spangler Noel L. Goddard David S. Thaler

BACKGROUND PCR in principle can detect a single target molecule in a reaction mixture. Contaminating bacterial DNA in reagents creates a practical limit on the use of PCR to detect dilute bacterial DNA in environmental or public health samples. The most pernicious source of contamination is microbial DNA in DNA polymerase preparations. Importantly, all commercial Taq polymerase preparations ine...

2014
Takeshi Yamagami Sonoko Ishino Yutaka Kawarabayasi Yoshizumi Ishino

DNA polymerases are widely used for DNA manipulation in vitro, including DNA cloning, sequencing, DNA labeling, mutagenesis, and other experiments. Thermostable DNA polymerases are especially useful and became quite valuable after the development of PCR technology. A DNA polymerase from Thermus aquaticus (Taq polymerase) is the most famous DNA polymerase as a PCR enzyme, and has been widely use...

Journal: :Methods in enzymology 2011
Daniel G Gibson

Three methods for assembling multiple, overlapping DNA molecules are described. Each method shares the same basic approach: (i) an exonuclease removes nucleotides from the ends of double-stranded (ds) DNA molecules, exposing complementary single-stranded (ss) DNA overhangs that are specifically annealed; (ii) the ssDNA gaps of the joined molecules are filled in by DNA polymerase, and the nicks ...

2010
H. Mir Mohammad Sadeghi R. Rajaei F. Moazen M. Rabbani A. Jafarian-Dehkordi

Taq DNA polymerase is widely used in laboratories and for this reason many investigators have focused their attention on understanding the role of various regions and amino acids in this enzyme. O-helix is a part of taq polymerase suggested to play an important role in the enzyme fidelity. The influence of Asn666 in this helix on the enzyme function has never been investigated, and therefore by...

Journal: :Buletin Veteriner Udayana 2022

Polymerase Chain Reaction (PCR) merupakan uji diagnostik yang sangat sensitif. Enzim Taq salah satu komponen paling penting dalam pengujian (PCR). taq polymerase harganya mahal. Penggunaan pada PCR kurang efisien. Untuk mengetahui efisiensi penggunaan enzim dan volume terkecil berapa masih dapat digunakan metode PCR, maka dilakukanlah penelitian dengan membuat lebih kecil (5µl, 10 µl, 25 µl) da...

Journal: :Nucleic acids research 1996
J Cline J C Braman H H Hogrefe

The replication fidelities of Pfu, Taq, Vent, Deep Vent and UlTma DNA polymerases were compared using a PCR-based forward mutation assay. Average error rates (mutation frequency/bp/duplication) increased as follows: Pfu (1.3 x 10(-6)) < Deep Vent (2.7 x 10(-6)) < Vent (2.8 x 10(-6)) < Taq (8.0 x 10(-6)) < < exo- Pfu and UlTma (approximately 5 x 10(-5)). Buffer optimization experiments indicated...

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