Used for first-strand cDNA synthesis with reverse transcriptase at temperatures of ≥50°C

Thermo Scientific™ Oligo(dT)₁₈ Primer is a synthetic single-stranded 18-mer oligonucleotide with 5'- and 3'-hydroxyl ends.

Primer is suitable for use in first-strand cDNA synthesis with reverse transcriptase

Serve as primers for DNA synthesis by a DNA polymerase or reverse transcriptase

Optimze cDNA synthesis with these random hexamer primers, oligo(dT)₁₈ primers and anchored oligo dT primers.

Sequence DNA fragments inserted into the MCS of various pUC19 based cloning vectors with M13 pUC sequencing primers, single-stranded oligonucleotides.

Oligonucleotides complementary to a DNA template are necessary to prime DNA synthesis for sequencing reactions

Perform sequencing of DNA fragments located downstream from the corresponding RNA polymerase promoter sequences in cloning vectors, such as pTZ19R, pTZ57R and pBluescript II.

Ambion pUC 19 DNA is digested to completion with Sau3A I

Perform highly efficient random priming of DNA synthesis reactions with this mixture of single-stranded random oligonucleotides.

Perform sequencing of DNA fragments located downstream from the corresponding RNA polymerase promoter sequences in cloning vectors, such as pTZ19R, pTZ57R and pBluescript II.

Truly random primers suitable for DNA synthesis using Klenow fragments with DNA templates or for cDNA synthesis using reverse transcriptase with mRNA templates

Perform sequencing of DNA fragments located downstream from the corresponding RNA polymerase promoter sequences in cloning vectors, such as pTZ19R, pTZ57R and pBluescript II.

When incorporated into DNA, 5-(3-aminoallyl)-dUTP provides a reactive group for addition of other chemical groups

Ideal for use as substrates as part of in vitro transcription reactions

Contain mixtures of linearized plasmids ready for use as templates as part of in vitro transcription reactions for synthesis of labeled RNA molecular size standards

Primers for sequencing of DNA fragments inserted into Eco32I site within the eco47IR gene of pJET1.2 and for colony screening by PCR.

5' Fluorescent Labeled Oligo

Contain mixtures of linearized plasmids ready for use as templates during in vitro transcription reactions for synthesis of labeled RNA molecular size standards

Sequence DNA fragments inserted into the MCS of various pUC19-based cloning vectors with M13 pUC sequencing primers, single-stranded oligonucleotides.

Perform sequencing of DNA fragments located downstream from the corresponding RNA polymerase promoter sequences in cloning vectors, such as pTZ19R, pTZ57R and pBluescript II.

Perform sequencing of DNA fragments located downstream from the corresponding RNA polymerase promoter sequences in cloning vectors, such as pTZ19R, pTZ57R and pBluescript II.

Ambion Lambda DNA is digested to completion with Hind III

Oligonucleotides complementary to a DNA template are necessary to prime DNA synthesis for sequencing reactions

Sequence DNA fragments inserted into the MCS of various pUC19 based cloning vectors with M13 pUC sequencing primers, single-stranded oligonucleotides.

Used for priming and reverse transcription of polyadenylated (poly A+) mRNA

Primers for sequencing of DNA fragments inserted into Eco32I site within the eco47IR gene of pJET1.2 and for colony screening by PCR.

Ideal for use as substrates as part of in vitro transcription reactions

Ambion Modified nucleotides confer unique characteristics to the RNA molecules into which they are incorporated

Provided at a stock concentration of 50μM