2' Fluoro RNA U 1000 nmol scale, 1 modification

2' Fluoro RNA U 1000 nmol scale, 1 modification

2' O-Me RNA Inosine 200 nmol scale, 1 modification

2' O-Me RNA Inosine 200 nmol scale, 1 modification

2' O-Me RNA Inosine 40 nmol scale, 1 modification

708,29 RON
2' O-Me RNA Inosine 40 nmol scale, 1 modification, Cod Catalog Eurogentec: MD-NB210-IN004
SKU
EUR_MD-NB210-IN004

2’O-Me RNA are partially resistant to a variety of ribo- and deoxyribonucleases. They form more stable hybrids with complementary RNA strands than equivalent DNA/RNA sequences. They are ideal for antisense probes.

Inosine is a nucleoside that occurs naturally in the wobble position of the anticodon of some transfer RNAs and is known to form base pairs with A, C and U during the translation process. Several experiments have suggested that deoxyinosine might be an “inert” base, its presence in an oligonucleotide sequence seems neither to disturb DNA duplex formation nor to destabilize the duplex. Independent of sequence effects, the order of base-pairing stabilities is I-C >> I-A > I-T = I-G. Deoxyinosine containing primers have been used successfully to amplify cDNA or genomic fragments for the generation of DNA probes from a peptide sequence.

 

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Description

2’O-Me RNA are partially resistant to a variety of ribo- and deoxyribonucleases. They form more stable hybrids with complementary RNA strands than equivalent DNA/RNA sequences. They are ideal for antisense probes.

Inosine is a nucleoside that occurs naturally in the wobble position of the anticodon of some transfer RNAs and is known to form base pairs with A, C and U during the translation process. Several experiments have suggested that deoxyinosine might be an “inert” base, its presence in an oligonucleotide sequence seems neither to disturb DNA duplex formation nor to destabilize the duplex. Independent of sequence effects, the order of base-pairing stabilities is I-C >> I-A > I-T = I-G. Deoxyinosine containing primers have been used successfully to amplify cDNA or genomic fragments for the generation of DNA probes from a peptide sequence.