Primer is suitable for use in first-strand cDNA synthesis with reverse transcriptase Oligo(dT)12 18 Primer, 25 µg

Optimze cDNA synthesis with these random hexamer primers, oligo(dT)₁₈ primers and anchored oligo dT primers. RANDOM HEXAMER 100UM 120UL

Truly random primers suitable for DNA synthesis using Klenow fragments with DNA templates or for cDNA synthesis using reverse transcriptase with mRNA templates RANDOM PRIMERS,1.5MM 9 units

Thermo Scientific™ Oligo(dT)₁₈ Primer is a synthetic single-stranded 18-mer oligonucleotide with 5'- and 3'-hydroxyl ends. OLIGO(DT)18 PRIM 100UM 60UL

Serve as primers for DNA synthesis by a DNA polymerase or reverse transcriptase Applied Biosystems® Random Hexamers (50 µM), 1 Kit

Template primers POLY (A) 100 MG

Used for first-strand cDNA synthesis with reverse transcriptase at temperatures of ≥50°C OLIGO DT(20) PRIMER

Primers for PCR amplification that complement many vectors PRIMER, T7Invitrogen offers primers for PCR amplification

Oligonucleotides complementary to a DNA template are necessary to prime DNA synthesis for sequencing reactions 2UG PRIM,M13(-20)FORWARD

Oligonucleotides complementary to a DNA template are necessary to prime DNA synthesis for sequencing reactions 2UG PRIM,M13 REVERSE

Sequence DNA fragments inserted into the MCS of various pUC19-based cloning vectors with M13 pUC sequencing primers, single-stranded oligonucleotides. M13/PUC REV PR -26 10UM 6NMOL

Custom 5' labeled primers are fluorescently labeled oligos with a choice of dye on the 5' end TA PCRII DUAL PROMOTER

Provided at a stock concentration of 50μM Oligo (dT) Primer (50 µM), 80 µL

Primers for sequencing of DNA fragments inserted into Eco32I site within the eco47IR gene of pJET1.2 and for colony screening by PCR. PJET1.2 FW 10UM 8.7 NMOL

Perform sequencing of DNA fragments located downstream from the corresponding RNA polymerase promoter sequences in cloning vectors, such as pTZ19R, pTZ57R and pBluescript II. SP6 PRIM 24-MER 10UM 4.2NMOL

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 RNA CENTURY MARKER TMPLT 5UG

Ideal for use as substrates as part of in vitro transcription reactions 75 mM Bio-11-UTP,30 µL

Perform sequencing of DNA fragments located downstream from the corresponding RNA polymerase promoter sequences in cloning vectors, such as pTZ19R, pTZ57R and pBluescript II. T3 PRIMER 24-MER 10UM 4.2NMOL

When incorporated into DNA, 5-(3-aminoallyl)-dUTP provides a reactive group for addition of other chemical groups 5-(3-aminoallyl)-dUTP (50 mM), each

Accurately sequence DNA with M13 pUC sequencing primers, single-stranded oligonucleotides with 5'-hydroxyl and 3'-hydroxyl ends. M13/PUC PRIM -20 10UM 6NMOL

Provided at a stock concentration of 50μM, and functionally tested using the RETROscript™ Kit Random Decamers (50 µM),80 µL

Ambion Modified nucleotides confer unique characteristics to the RNA molecules into which they are incorporated 5-(3-aminoallyl)-UTP (50 mM), each

Used for priming and reverse transcription of polyadenylated (poly A+) mRNA Oligo d(T)16 (50 µM), 1 Kit

Ideal for use as substrates as part of in vitro transcription reactions 10 mM Bio-11-UTP,25 µL

Sequence DNA fragments inserted into the MCS of various pUC19 based cloning vectors with M13 pUC sequencing primers, single-stranded oligonucleotides. M13/PUC PRIM -46 10UM 4.5NMOL

Sequence DNA fragments inserted into the MCS of various pUC19 based cloning vectors with M13 pUC sequencing primers, single-stranded oligonucleotides. M13/PUC REV -46 10UM 4.2NMOL

Ambion pUC 19 DNA is digested to completion with Sau3A I pUC19 DNA - Sau3A I digested, 50 µg

Perform highly efficient random priming of DNA synthesis reactions with this mixture of single-stranded random oligonucleotides. EXO-RES RANDOM PR 500UM 100UL

Contain mixtures of linearized plasmids ready for use as templates during in vitro transcription reactions for synthesis of labeled RNA molecular size standards RNA CENTURY MRKR TEMP PLUS 5UG

Perform sequencing of DNA fragments located downstream from the corresponding RNA polymerase promoter sequences in cloning vectors, such as pTZ19R, pTZ57R and pBluescript II. T7 PRIMER 20-MER 10UM 5NMOL