Unlabelled Oligonucleotides and Primers
Applied Biosystems™ Random Hexamers (50 µM)
Serve as primers for DNA synthesis by a DNA polymerase or reverse transcriptase
Invitrogen™ Random Primers
Truly random primers suitable for DNA synthesis using Klenow fragments with DNA templates or for cDNA synthesis using reverse transcriptase with mRNA templates
Invitrogen™ Oligo(dT)20 Primer
Used for first-strand cDNA synthesis with reverse transcriptase at temperatures of ≥50°C
Thermo Scientific™ Random Hexamer Primer
Optimze cDNA synthesis with these random hexamer primers, oligo(dT)18 primers and anchored oligo dT primers.
Thermo Scientific™ Oligo(dT)18 Primer
Thermo Scientific™ Oligo(dT)18 Primer is a synthetic single-stranded 18-mer oligonucleotide with 5'- and 3'-hydroxyl ends.
Invitrogen™ Oligo(dT)12-18 Primer
Primer is suitable for use in first-strand cDNA synthesis with reverse transcriptase
Cytiva (Formerly GE Healthcare Life Sciences) RNA Homopolymers
Template primers
Invitrogen™ Oligo (dT) Primer (50 µM)
Provided at a stock concentration of 50μM
Invitrogen™ M13 Forward (-20)
Oligonucleotides complementary to a DNA template are necessary to prime DNA synthesis for sequencing reactions
Invitrogen™ T7 Promoter Primer
Primers for PCR amplification that complement many vectors
Thermo Scientific™ Exo-Resistant Random Primer
Perform highly efficient random priming of DNA synthesis reactions with this mixture of single-stranded random oligonucleotides.
Applied Biosystems™ Human, Forward Primer, Desalted
Human, Forward Primer, Desalted
Cytiva (Formerly GE Healthcare Life Sciences) Poly(I)-Poly(C)
For stimulation of interferon production in vitro. Cytiva Poly(I)-Poly(C) is supplied as a sterile lyophilised powder.
Thermo Scientific™ T7 promoter Sequencing Primer, 20-mer
Perform sequencing of DNA fragments located downstream from the corresponding RNA polymerase promoter sequences in cloning vectors, such as pTZ19R, pTZ57R and pBluescript II.
Thermo Scientific™ M13/pUC Reverse Sequencing Primer (-26), 17-mer
Sequence DNA fragments inserted into the MCS of various pUC19-based cloning vectors with M13 pUC sequencing primers, single-stranded oligonucleotides.
Applied Biosystems™ Human, Reverse Primer, Desalted
Human, Reverse Primer, Desalted
Thermo Scientific™ M13/pUC sequencing primer (-20), 17-mer
Accurately sequence DNA with M13 pUC sequencing primers, single-stranded oligonucleotides with 5'-hydroxyl and 3'-hydroxyl ends.
Invitrogen™ Random Decamers (50 µM)
Provided at a stock concentration of 50μM, and functionally tested using the RETROscript™ Kit
IBA Solutions for Life Science™ Competent Cells E. coli TOP10
Cells are highly efficient and ideally suited for the StarGate™ applications
Invitrogen™ Lambda Hind III dsDNA Markers
Ambion Lambda DNA is digested to completion with Hind III
Invitrogen™ 5-(3-Aminoallyl)-UTP (50 mM)
Ambion Modified nucleotides confer unique characteristics to the RNA molecules into which they are incorporated
Invitrogen™ pUC19 DNA (Sau3A I digested)
Ambion pUC 19 DNA is digested to completion with Sau3A I
Thermo Scientific™ SP6 promoter Sequencing Primer, 18-mer
Perform sequencing of DNA fragments located downstream from the corresponding RNA polymerase promoter sequences in cloning vectors, such as pTZ19R, pTZ57R and pBluescript II.
Thermo Scientific™ pJET1.2 Reverse Sequencing Primer, 24-mer
Primers for sequencing of DNA fragments inserted into Eco32I site within the eco47IR gene of pJET1.2 and for colony screening by PCR.
Thermo Scientific™ pJET1.2 Forward Sequencing Primer, 23-mer
Primers for sequencing of DNA fragments inserted into Eco32I site within the eco47IR gene of pJET1.2 and for colony screening by PCR.
Invitrogen™ Bio-16-UTP (10 mM)
Ideal for use as substrates as part of in vitro transcription reactions
Invitrogen™ Bio-11-UTP (75 mM)
Ideal for use as substrates as part of in vitro transcription reactions
Applied Biosystems™ Oligo d(T)16 (50 µM)
Used for priming and reverse transcription of polyadenylated (poly A+) mRNA
Invitrogen™ Anchored Oligo(dT)20 Primer
Primer mixture consisting of a string of 20 deoxythymidylic acid residues followed by dV (either dG, dA, or dC) and then by dN (dA, dT, dG, or dC)