Chemical reagents and other products used for DNA-related techniques and processes such as PCR cloning, DNA sequencing, DNA cloning and mapping, mutagenesis, DNA synthesis, etc.; includes kits, columns, buffers, labelling technology, and others.
Efficiently clone PCR products generated with any thermostable DNA polymerase using Thermo Scientific™ CloneJET™ PCR Cloning Kit, a positive selection system.
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An advanced positive-selection system for high-efficiency cloning of PCR products generated with any thermostable DNA polymerase. Any blunt or sticky-end DNA fragment can be cloned.
The Invitrogen Collibri PCR-free PS DNA Library Preparation kits are designed for next-generation sequencing (NGS) on Illumina systems. The kit supports whole-genome sequencing (WGS) applications and is suitable for all genomes, including FFPE samples.
The PCR Product Pre-Sequencing Kit uses a novel, enzymatic clean-up method to pre-treat PCR products prior to sequencing, without any subsequent purification or separation steps.
Our fastest PCR clean-up method - just 5 minutes to superior sequencing results. Now available with optional tracking dye. It is necessary to remove excess primers and unincorporated nucleotides from the PCR reaction prior to sequencing.
The DNA contained in the preparation has been lyophilized to maximize stability.The two hydrolytic enzymes used in this kit, shrimp alkaline phosphatase and exonuclease I, effectively remove excess dNTPs and primers.
The matrix standard set DS-32 is used to generate the 'multicomponent matrix' required when analyzing 5-FAM™, JOE™, NED™, and ROX™ labeled DNA fragments on the Applied Biosystems™ 31xx, 3500 and 3730 Series Systems.
Use for synthesis of first-strand cDNA templates from total RNA or polyadenylated RNA using a primer of choice. Cytiva Life Sciences™ Ready-to-Go™ You-Prime First-Strand Beads are perfect for RT-PCR applications.
Efficiently clone PCR products generated with any thermostable DNA polymerase using Thermo Scientific™ CloneJET™ PCR Cloning Kit, a positive selection system.
Cloning of blunt-end or 3'-dA tailed PCR products up to 10kb; Cloning of DNA fragments generated by restriction enzymes; Sequencing of cloned DNA; In vitro and in vivo transcription of cloned inserts from the T7 promoter