Expression Recovery Medium
Optimised formulation for ensuring stability and high-efficiency transformation of protein expression clones.
Optimised formulation for ensuring stability and high-efficiency transformation of protein expression clones.
Classic protected DNA nucleoside phosphoramidite.
Phosphoramidite useful for synthesising 2'-5' linked oligonucleotides.
Allows for incorporation of a halogenated nucleoside into oligonucleotides for crystallographic studies and crosslinking studies of protein-DNA and RNA-DNA complexes.
Fluorous-tagged nucleoside useful for the purification of oligonucleotides.
CPG synthesis column for incorporation of unmodified dA at 3' end of an oligonucleotide.
CPG synthesis column for incorporation of unmodified dA at 3' end of an oligonucleotide.
CPG column for the incorporation of an (otherwise unmodified) reverse (5' to 3') dA nucleobase at the 3' end of an oligonucleotide.
Commonly used protected DNA nucleoside phosphoramidite.
CPG synthesis column for incorporation of unmodified dA at 3' end of an oligonucleotide.
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