Abstract: The present invention provides methods for rapidly identifying an RNA viral infection using an isothermal nucleic acid amplification reaction that can be carried out on extracted RNA in the context of a crude biological sample.

Abstract: The present invention features compositions and methods for amplifying a target oligonucleotide in a sample, including detection of the target oligonucleotide in real time.

Abstract: The present invention provides methods for rapidly identifying an RNA viral infection using an isothermal nucleic acid amplification reaction that can be carried out extracted RNA in the context of a crude biological sample.

Abstract: The present invention features compositions and methods for amplifying a target oligonucleotide in a sample, including detection of the target oligonucleotide in real time.

Abstract: The disclosure relates to a method for improving the selectivity of a membrane, specifically of a membrane comprising a blend of i) a polysulfone, polyethersulfone or polyarylethersulfone and ii) polyvinylpyrrolidone, characterized in that the membrane is coated with polydopamine and heparin in a one-step or two-step reaction or by in situ modification with polydopamine followed by coating with heparin. The disclosure further relates to a process for producing such modified membranes having an improved selectivity, and to a filtration/diffusion device comprising the membrane which can be used, for example, in hemodialysis applications.

Abstract: The present invention relates to high performance, crosslinked hollow-fibre membranes and a new process for manufacturing the same.

Abstract: The present invention features compositions and methods for amplifying a target oligonucleotide in a sample, including detection of the target oligonucleotide in real time.

Abstract: The present invention features compositions and methods for amplifying a target oligonucleotide in a sample, including detection of the target oligonucleotide in real time.

Abstract: The present invention relates to high performance, crosslinked hollow-fibre membranes and a new process for manufacturing the same.

Abstract: The present invention provides methods for rapidly identifying an RNA viral infection using an isothermal nucleic acid amplification reaction that can be carried out extracted RNA in the context of a crude biological sample.

Abstract: The present invention provides methods for rapidly identifying an RNA viral infection using an isothermal nucleic acid amplification reaction that can be carried out extracted RNA in the context of a crude biological sample.

Abstract: The invention relates to a method for producing halogen-N,N-dimethylbenzylamines wherein halogen=chlorine or bromine, preferably chloro-N,N-dimethylbenzylamines, preferably ortho-chloro-N,N-dimethylbenzylamine (o-Cl-DMBA), by reductive amination in the absence of sulfur.

Abstract: The present invention provides methods for rapidly identifying an RNA viral infection using an isothermal nucleic acid amplification reaction that can be carried out extracted RNA in the context of a crude biological sample.

Abstract: The present invention features compositions and methods for amplifying a target oligonucleotide in a sample, including detection of the target oligonucleotide in real time.

Abstract: The invention relates to a method for producing halogen-N,N-dimethylbenzylamines wherein halogen=chlorine or bromine, preferably chloro-N,N-dimethylbenzylamines, preferably ortho-chloro-N,N-dimethylbenzylamine (o-Cl-DMBA), by reductive amination in the absence of sulfur.

Abstract: In a method for jointly tempering reaction samples in at least two steps in assigned, specified temperature ranges, which are repeatedly carried out consecutively as sequences of steps, in a randomly selected first step, several first groups of samples, in each case containing at least one sample are brought to temperatures, which are the same within the group and different between the groups within the first temperature range assigned to the first step, in a randomly selected step of the sequence, if the reaction product is affected by the two steps with regard to identical evaluation parameters, at east one of the first groups at least two of the samples belong to different groups are brought to temperatures, which are the same within the groups and different between the groups, within the temperature range assigned to the second step, and, if the evaluation parameters are different, at least two random samples belong to different third groups, which are brought to temperatures, which are the same within gr

Abstract: A laboratory tempering device for jointly tempering reaction samples in at least two steps in assigned, specified temperature ranges, which are repeatedly carried out consecutively as sequences of steps, the laboratory tempering device, in a randomly selected first step, at the sequence bringing several first groups of samples, in each case containing at least one sample, to temperatures, which are the same within the group and different between the groups within the first temperature range assigned to the first step, wherein, in a randomly selected step of the sequence, if the reaction product is affected by the two steps with regard to identical evaluation parameters, for at least one of the first groups at least two of the samples belong to different groups, which are brought to temperatures, which are the same within the groups and different between the groups, within the temperature range assigned to the second step, and, if the evaluation parameters are different, at least two random samples belong to d