DNA Template Preparation for PCR

General description The N-CMV-30 sequencing primer is a chemically synthesized, 30 base, single strand oligodeoxyribonucleotide designed for dsDNA or ssDNA sequencing of FLAG &#174: fusion proteins at the C-terminus of the pFLAG-CMV expression

Product content: :Component:N665917-1ml:N665917-5ml:2×SYBR qPCR MasterMix:1 ml:5×1 ml:qPCR Primer Mix:100 µl:500 µl:DNA Standard A:100 µl:500 µl:DNA Standard B:100 µl:500 µl:DNA Standard C:100 µl:500 µl:DNA Standard D:100 µl:500 µl:DNA Standard

Product content: :Component:N665917-1ml:N665917-5ml:2×SYBR qPCR MasterMix:1 ml:5×1 ml:qPCR Primer Mix:100 µl:500 µl:DNA Standard A:100 µl:500 µl:DNA Standard B:100 µl:500 µl:DNA Standard C:100 µl:500 µl:DNA Standard D:100 µl:500 µl:DNA Standard

NH₄ Buffer for use in PCR with DNA polymerases. Product Highlights Ready-to-use - 10x (NH₄)₂SO₄ buffer for PCR Optimized - to improve PCR amplification rates Reproducibility - helps provide consistent

Nova Taq DNA polymerase is a recombinant form of Thermus aquaticus DNA polymerase. This enzyme is a non-proofreading DNA polymerase.

Nova Taq DNA polymerase is a recombinant form of Thermus aquaticus DNA polymerase. This enzyme is a non-proofreading DNA polymerase.

Nova Taq DNA polymerase is a recombinant form of Thermus aquaticus DNA polymerase. This enzyme is a non-proofreading DNA polymerase.

One Step M-MULV RT-PCT Kit: One-Step M-MuLV RT-PCR offers a unique system for performing RT-PCR in a single step, in a single tube. Traditionally, RT-PCR is performed in two reaction steps.

Biochem/physiol Actions Human PC4 is a non-TAF transcription coactivator that mediates activator-dependent transcription by RNA polymerase II in vitro through most tested activators. The function of PC4 is through interactions with

PCDNA3.1(-)/MYC-HIS C/LACZ CONTROL VECTOR

BRAND PCR tube strips are manufactured from high-quality virgin plastics for excellent, reproducible results in most PCR applications. These tube strips are manufactured without lubricants or chemical additives that can contaminate reagents and

Optimized PCR buffer set for amplification of specific DNA fragments in conventional PCRs ( i.e .