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Pcr product purification kit

Manufactured by Bioneer

The PCR product purification kit is a laboratory equipment designed to purify and concentrate DNA amplified through the polymerase chain reaction (PCR) process. It removes unwanted reagents, primers, and non-specific amplification products, allowing for the isolation of the desired PCR product.

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3 protocols using pcr product purification kit

1

Heterologous expression of Cohnella sp. A01 proteins

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Pfu DNA polymerase, RNase A, Nde I and Not I, T4 DNA ligase, α-chymotrypsin, pepsin, trypsin, proteinase K and DNA ladder were purchased from Fermentase. Nessler reagent (CAS Number: 7783-33-7), kanamycin (K1377–5G), agarose (A9539–50G) ANS (A 1028) were provided from sigma Aldrich Co (Steinheim, USA). Anti poly-Histidine-HRP antibody was purchased from sigma (A7058). Protein molecular mass marker, IPTG, amino acids, DTT, BME, GSH, ascorbic acid, iodoacetate, iodoacetamide were acquired from Merck. DNA extraction kit was purchased from Peqlab and PCR product purification kit was obtained from BioNEER (Seoul, Korea). Ni-NTA resin was purchased from Invitrogen (Carlsbad, USA). E. coli DH5α and BL21 (DE3) strains and pET-26b vector resistant to kanamycin were purchased from Invitrogen (Carlsbad, USA). All experiments were replicated at least three times.
Cultivation of Cohnella sp. A01, was carried out at 55 °C in LB medium for 4 days and it΄s genomic DNA was extracted using the high pure DNA extraction kit. E. coli strains containing pET-26b vector were cultured at 37 °C in LB with final concentration 30 μg/ml of kanamycin. LB plates were solidified with 1.5% agar in the presence and absence of kanamycin to perform respectively contamination and viability tests.
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2

PCR Product Sequencing and Analysis

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The PCR products of target genes were amplified and purified using a PCR product purification kit from Bioneer (Seoul, Korea). Table S1 reveals the primer sequences used in this work. DNA sequences were determined by the DNA sequencing facility of Macrogen (Seoul, Korea). Nucleotide point mutations and frameshifts were identified by Blast analysis using BioEdit and ClustalW (http://www.genome.jp/tools-bin.clustalw).
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3

DNA Sequencing and BLAST Analysis

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The single amplicons obtained from PCR were sequenced using an ABI 373 0XL DNA analyzer (Perkin Elmer, USA). A single DNA band was purified using a PCR product purification kit (Bioneer, Korea) and amplified using ABI BigDye Terminator v3.1 Cycle-Sequencing Kit for DNA sequencing. The DNA sequences were further analyzed using the BLAST program provided by the NCBI GenBank database.
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