Anchor oligo d(T) is a synthetic 20-mer single-stranded DNA oligonucleotide.

It consists sequentially of 18 dT nucleotides, followed by two additional ones - VN, where V represents dA, dC or dG, and N represents dA, dC, dG or dT.

Due to the variable terminal sequence, it prevents binding within the poly(A) tail, allowing more efficient cDNA synthesis for labeling, first-strand synthesis and RT-PCR applications.

Ready to use, optimized mixture of random hexamers and oligo(dT)₁₈ primers. This mixture provides optimal and uniform coverage of the RNA sample, for a wide range of concentrations of RNA templates. Unlike the traditional use of hexamers as primers, this method improves coverage of the 3'-end of the RNA template.

Ready-to-use, optimized mixture of random 9-mer (nona) and oligo(dT)₁₈ primers. This mixture provides optimal and uniform coverage of the RNA sample, for a wide range of concentrations of RNA templates. In contrast to the traditional use of random primers for cDNA production, this method improves coverage of the 3' end of the RNA template.

The oligonucleotide was purified by ion exchange chromatography, desalted and freeze-dried.

Does not contain foreign impurities of salts.

The structure of the oligonucleotide was confirmed by HPLC-MS.

The functional activity of d(T)₁₈ was confirmed by PCR.

Random Primer 9 is desalted and freeze dried.

Does not contain foreign impurities of salts.

Molecular weight distribution confirmed by HPLC-MS.

Functional activity confirmed by PCR.

Random Primer 6 is desalted and freeze dried.

Does not contain foreign impurities of salts.

Molecular weight distribution confirmed by HPLC-MS.

Functional activity confirmed by PCR.