Abstract: The invention relates to a coupling unit for coupling an optical transmitting and/or receiving module to an optical fiber. The coupling unit has a connecting area that can be connected to a transmitting and/or receiving module, and a holding area that holds an optical fiber. A transparent coupling area is provided, which is formed as an integral component of the coupling unit, and via which light can be coupled directly between an optical fiber that is inserted into the holding area and a transmitting and/or receiving module that is coupled directly to it. The coupling area preferably has a matched refractive index. The coupling unit is preferably in the form of an injection-molded part.

Abstract: The present invention is in the field of nucleic acid binding compounds comprising 7-substituted 7-deaza-8aza-2,6-diamino-purine bases, compounds useful for the preparation of such compounds, various uses thereof and methods for the determination of nucleic acids using said compounds in the field of diagnostics.

Abstract: The invention relates to novel monomeric building blocks for labeling peptide nucleic acids and similarly constructed nucleic acid-binding oligomers possessing groups which are coupled to a nitrogen base and/or to the peptide backbone of the peptide nucleic acid. The invention furthermore relates to peptide nucleic acids which contain at least one labelled monomeric building block.

Abstract: A method for detecting nucleic acids by binding a probe P to a partial sequence S contained in the nucleic acid to produce a binding product B1, degrading the nucleic acid to produce a binding product B2 containing a partial nucleic acid F of a defined length and detecting the binding product B2 or the partial nucleic acid F a part based on its mass is particularly suitable for the parallel detection of nucleic acid of different sequences.

Abstract: Aerobically hardening adhesives based on polymers of acrylates or methacrylates having a relatively high boiling point such as polyurethane (meth)acrylates are described, wherein the adhesives contain at least one initiator capable of forming free radicals, at least one accelerator, and at least one siccative. Such adhesives are largely odorless and harden completely such that the adhesive surface at the boundary with air is not tacky.

Abstract: A process for the chemical synthesis of oligonucleotidesUse of a dansylethoxycarbonyl group as base-labile 5'-hydroxyl protective group in the chemical synthesis of DNA and RNA and suitable synthetic processes.The ease of detection of the dansyl protective group and the ease of elimination from the sugar residue of the nucleotide without side reactions make oligonucleotide synthesis possible with high yields in very small quantities.

Abstract: The invention pertains to an aerobically curing composition comprising free-radical polymerizable compounds, an activator system, and optionally conventional additives, characterized in that said composition contains as said free-radical polymerizable compounds at least one polyurethane (meth)acrylate one or more (meth)acrylate comonomers; wherein said composition contains from 20 to 80% by weight of said polyurethane (meth)acrylate and from 80 to 20% by weight of said (meth)acrylate comonomer(s), based on the total of polymerizable compounds, and said activator system is a hydrazone activator system, as well as the preparation and use of said composition.

Abstract: A reaction adhesive becomes porous after hardening. This allows both small and larger gaps to be sealed between the bonded substrates, as the liquid adhesive has a low to medium viscosity and the hardened glue shows a marked volume increase. Reaction adhesives based on (meth)acrylates and that contain azo-bis-isobutyronitrile as initiator and expanding agent are preferably used. The disclosed reaction adhesive is preferably used for gluing reactive coils.

Abstract: Use of a dansylethoxycarbonyl group as base-labile 5'-hydroxyl protective group in the chemical synthesis of DNA and RNA and suitable synthetic processes.The ease of detection of the dansyl protective group and the ease of elimination from the sugar residue of the nucleotide without side reactions make oligonucleotide synthesis possible with high yields in very small quantities.

Abstract: Dansylethoxycarbonyl (Dans-EOC) groups which can be employed as base-labile 5'hydroxyl protective groups in chemical oligonucleotide synthesis are disclosed. These groups allow the preparation of a compound of the formula (I) ##STR1## which comprises reacting the compound of the formula (II) ##STR2## with a chlorocarbonyl donor.