Abstract: A projection arrangement for a head-up display (HUD), includes a composite pane, including an outer and an inner pane connected to one another via a thermoplastic intermediate layer, with an HUD region; an electrically conductive coating on the surface of the outer pane or of the inner pane facing or within the intermediate layer; and a projector directed toward the HUD region. The radiation of the projector is p-polarised. The composite pane has reflectance of at least 10% relative to p-polarised radiation in the spectral range from 450 nm to 650 nm. The electrically conductive coating includes at least four electrically conductive layers, which are each arranged between two dielectric layers or layer sequences. The sum of the thicknesses of all electrically conductive layers is at most 30 nm and at least one of the electrically conductive layers has a thickness of at most 5 nm.

Abstract: The invention relates to method for loading microorganisms or parts thereof on and/or in pre-synthesized multiphase biomaterials comprising nanocellulose wherein the microorganisms are resuspended in a buffer or a culture medium and loaded into and/or onto the multiphase biomaterial and the use of such a loaded multiphase biomaterial in nutritional, food, pharmaceutical, medical, cosmetic, especially oral, mucosal, dermal and transdermal, ocular, dermatological or female health applications.

Abstract: A method for loading one or more microorganisms or parts thereof on and/or in pre-synthesized multiphase biomaterials including nanocellulose wherein the microorganisms are resuspended in a buffer or a culture medium and loaded into and/or onto the multiphase biomaterial. Uses of such loaded multiphase biomaterials may be in nutritional, food, pharmaceutical, medical, cosmetic, especially oral, mucosal, dermal and transdermal, ocular, dermatological, or female health applications.

Abstract: The aim of the invention is to dry cellulose and cellulose-containing materials in the shortest possible time and with the lowest possible technical costs, without disruptive stress on the cellulose and without loss of stability and efficacy of any additive substances, for example medicaments, and to reswell it as required almost completely to the original structure and consistency. According to the invention for the purpose of drying and obtaining the swellability with almost complete reconstitution of the cellulose structure and consistency the dried cellulose to be prepared or the cellulose-containing material is subjected to the adsorbent effect of a moisture binder, in particular an osmotically and/or hygroscopically effective solution and then dried regardless of any structural change to the material.

Abstract: The invention relates to low molecular weight polyethylenimines, to vectors for inserting nucleic acids into cells which contain low molecular weight polyethylenimines, and to the preparation and use of the low molecular weight polyethylenimine and the vector. The invention relates to a vector for inserting a nucleic acid into a cell, which vector contains a low molecular weight polyethylenimine (LMW PEI) and a nucleic acid, with the LMW PEI having a molecular weight of less than 50,000 Da.

Abstract: The invention relates to low molecular weight polyethylenimines, to vectors for inserting nucleic acids into cells which contain low molecular weight polyethylenimines, and to the preparation and use of the low molecular weight polyethylenimine and the vector. The invention relates to a vector for inserting a nucleic acid into a cell, which vector contains a low molecular weight polyethylenimine (LMW PEI) and a nucleic acid, with the LMW PEI having a molecular weight of less than 50,000 Da.

Abstract: A conjugate or compound comprising polyethyleneglycol and an oligonucleotide, wherein at least one polyethyleneglycol is linked to the 5?-end of the oligonucleotide and at least one polyethyleneglycol is linked to the 3?-end of the oligonucleotide, wherein the molecular weight of the polyethyleneglycol linked to the 5?- and 3?-end of the oligonucleotide is identical and is <5000 Da, or wherein the molecular weight of the polyethyleneglycol linked to the 5?- and 3?-end of the oligonucleotide is different.

Abstract: The invention relates to cationic block copolymers of formula A(-X-B)n, wherein A represents a hydrophilic polymer, B represents polyethyleneimine (PEI), X represents a bridge, n represents 1-200. The invention also relates to methods for producing the inventive cationic block polymers and to their use e.g. as a tenside and for complexing nucleic acids.

Abstract: The invention relates to cationic block copolymers of formula A(—X—B)n or C(—Y—D)m, wherein A represents a hydrophilic polymer, B represents polyethyleneimine (PEI), X represents a bridge, n represents 1-200, C represents PEI, D represents the residue of a polyethylene glycol, Y represents a bridge and m represents 1-200. The invention also relates to methods for producing the inventive cationic block polymers and to their use e.g. as a tenside and for complexing nucleic acids.

Abstract: The invention relates to the complexation of RNA with optionally modified polyethylenimines for extracellular and intracellularin vitro and in vivo stabiliztion thereof and for cellular introduction of the complexed RNA in cells. The invention also relates to chemically modified or non-modified, natural or synthetic ribozymes complexes and polyethylenimine (PEI) having any chain length, molar mass and degree of branching, which is chemically modified or non-chemically modified. The invention further relates to the production of complexes and to the use thereof in the protection of RNA against enzymatic and non-enzymatic degradation and their reception in vitro or in vivo in cells. The biological activity of the ribozymes remains intact.

Abstract: The invention relates to low molecular weight polyethylenimines, to vectors for inserting nucleic acids into cells which contain low molecular weight polyethylenimines, and to the preparation and use of the low molecular weight polyethylenimine and the vector.