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Fastpfu buffer

WebNov 29, 2024 · The PCR reaction volume usually uses 50μl system and consists of 5–30ng Plasmid DNA or 100ng Genomic DNA, 1x TransEco FastPfu Buffer, 250μM dNTP, 0.4μM of each primer, 2.5U of TransEco FastPfu DNA Polymerase or Taq DNA polymerase and ddH 2 O up to 50μl. WebTransStart® FastPfu Fly DNA Polymerase Catalog Number:AP231-21 Price:$101.00 Specification: 250 units 500 units 6×500 units Quantity: Manual MSDS COA Inquire Now Buy Now Add to Cart Free Sample …

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WebMay 25, 2024 · The breeding systems were in a greenhouse at 27.5°C with 70% relative humidity. The larvae were fed with a mixture of wheat flour and bran every two days, and … WebThe PCR mixtures contain 5 × TransStart FastPfu buffer 4 μL, 2.5 mM dNTPs 2 μL , forward primer (5 μM) 0.8 μL, reverse primer (5 μM) 0.8 μL, TransStart FastPfu DNA Polymerase … pt. pharmasolindo https://roywalker.org

TransStart® FastPfu Fly DNA Polymerase ABIN5519533

WebNov 1, 2014 · The PCR reaction solution comprised 5 μM forward and reverse primers, 10 ng of template DNA, 2.5 mM dNTPs, 4 μl of 5× FastPfu Buffer and 0.4 μl of FastPfu Polymerase. Double distilled water was added to a final volume of 20 μl. WebConsequently, Pfu DNA Polymerase is recommended for use in PCR and primer extension reactions that require high-fidelity synthesis. Pfu DNA Polymerase-generated PCR fragments are blunt-ended. 10X Reaction Buffer with MgSO4: 200mM Tris-HCl (pH 8.8 at 25°C), 100mM KCl, 100mM (NH 4) 2 SO 4, 20mM MgSO 4, 1.0% Triton® X-100 and … WebDec 1, 2024 · The mobile phase consisted of acetonitrile as Solvent A and 1% formic acid as Solvent B. The gradient elution program of the solution include: 55% A at 0–20 min; … pt. orela shipyard

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Fastpfu buffer

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WebJul 5, 2024 · Methods: In this study, we systematically described the characteristics of bacteria in the oral and nasal niches in healthy children, CP children, healthy adolescents, CP adolescents, and postoperative adolescents by 454-pyrosequencing technology (V3–V6) to determine bacterial differences induced by CP. WebApr 28, 2024 · The raw materials used for PCR reaction were as follows: Transgen AP221–02:Transstart FastPFU DNA Polymerase, 20μL reaction system: 5 × TransStart FastPfu buffer (4μL), 2.5 mM dNTPs (2μL), forward primer (5μM) 0.8μL, reverse primer (5μM) 0.8μL, TransStart FastPfu polymerase 0.4μL,BSA 0.2μL, template DNA 10 ng, up …

Fastpfu buffer

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Webmixtures containing 4 lL of 5X FastPfu Buffer, 2 lL of 2.5 mM dNTPs, 0.8 lL of each primer (5 lM), 0.4 lL of FastPfu Polymerase, and 10 ng of template DNA. The PCR products were extracted from a 2% agarose gel and further purified using an AxyPrep DNA Gel Extraction Kit (Axygen Biosciences, Union City, CA, USA). The products were quantified using WebJan 30, 2024 · DNA samples were amplified in triplicate on an ABI GeneAmp ® 9700 PCR System (ABI, MA, USA) in PCR reactions containing 2 μl 2.5 mM dNTPs, 0.4 μl FastPfu Polymerase (Transgen Biotech, Beijing ...

WebSep 21, 2024 · The PCR reactions were conducted using the following program: 3 min of denaturation at 95°C, 27 cycles of 30 s at 95°C, 30 s for annealing at 55°C, and 45 s for elongation at 72°C, and a final extension at 72°C for 10 min. PCR reactions were performed in a triplicate 20 μL mixture containing 4 μL of 5 × FastPfu Buffer, 2 μL of 2.5 mM ... WebFastPfu FLY Sets Higher Standards of High-Fidelity DNA Polymerase Performance. Whereas Phusion and Q5 failed, FastPfu FLY succeeded easily at... 1-877-661-4711 …

WebApr 14, 2024 · Twenty-microliter bacteria/fungi mixtures for PCR contained 4 μL of 5× TransStart FastPfu buffer/2 μL of 10× Buffer, 2.5 mM dNTPs in 2 μL, 0.8 μL of forward primer (5 μM), 0.8 μL of reverse primer (5 μM), 0.4 μL of FastPfu Polymerase/0.2 μL of rTaq Polymerase, 0.2 μL of BSA, 10 ng of template DNA, and finally ddH2O up to 20 μL, with … WebA: In a 10 µl reaction as follows: add purified PCR product, 0.2 μl of Taq DNA Polymerase, 0.5 μl of 10 mM dNTP (or 0.5 μl of 2.5 mM dATP) and 1 μl of 10xTaq Buffer. Incubate at 72°C for 5–15 minutes. TransFast ® Taq DNA Polymerase EasyTaq ® DNA Polymerase EasyTaq ® DNA Polymerase for PAGE TransTaq ®-T DNA Polymerase

WebMar 8, 2024 · We then collected below-ground root biomass to a depth of 30 cm using soil cores (diameter 7 cm) in each of these five quadrats as well. Roots were collected by …

Web本发明公开一种基于环境DNA技术监测淡水底栖动物群落多样性的方法,包括步骤:(1)采集表层水样;(2)水样过滤与eDNA提取;(3)PCR扩增;(4)高通量测序,获得OTU的代表序列;(5)底栖动物比对数据库的建立;(6)比对建立的底栖动物数据库,对待测样品OTUs代表性序列进行物种注释。本发明取样简单、人力 ... hot def scrabbleWeb侯 磊,薛 蓓,薛会英 (西藏农牧学院,西藏 林芝 860000) 土壤线虫作为土壤动物中的优势类群,是草地生态系统中的消费者,关系到草地生产力的增减[1]。 pt. osell selection indonesiaWebEach batch of TransStart® FastPfu DNA Polymerase has been assayed for amplification efficiency to amplify p53 gene from 10 ng of human genomic DNA. Restrictions For … pt. opelon garment indonesiaWebProduct Details. TransStart® FastPfu DNA Polymerase is a fast, high fidelity and high processivity hot start DNA polymerase. • Extension rate is about 2-4 kb/min. • … hot demon boy minecraft skinsWebMar 11, 2024 · A 20-μL PCR reaction system contained 4 μL of 5 × FastPfu Buffer, 2 μL of 2.5 mM dNTPs, 0.8 μL each of the 338F and 806R primers, 0.4 μL of FastPfu polymerase, 10 ng of template DNA, 0.2 μL of BSA, and residual ddH 2 O. pt. oryx servicesWebDec 14, 2024 · The PCR mixtures contained 5 × TransStart FastPfu buffer 4 μL, 2.5 mM dNTPs 2 μL, forward primer (5 μM) 0.8 μL, reverse primer (5 μM) 0.8 μL, TransStart FastPfu DNA Polymerase 0.4 μL, template DNA 10 ng, and, finally, ddH 2 O up to 20 μL. PCR assays were performed in triplicate. pt. oto multiarthaWebMay 1, 2024 · Fresh soil samples were divided into two subsamples, one of which was stored at 4 °C before determination of physicochemical properties, and the other was … pt. pacinesia chemical industry