Finden Sie schnell roto dachfenster insektenschutzrollo für Ihr Unternehmen: 5 Ergebnisse

Sie wünschen den Einbau neuer Fenster? Wir arbeiten mit namhaften Herstellern wie Velux zusammen und garantieren nachhaltig Qualität und Sicherheit. Die meisten Dachfenster sind auch bekannt als Klapp-Schwingfenster und werden bevorzugt von Dachdeckermeistern eingebaut. Dachdecker verfügen in diesem Bereich über wesentlich mehr Erfahrungen als klassische Fensterbauer. Lassen Sie sich also von einem Dachdeckermeister beraten, der hunderte Dachfenster installiert hat und über langjährige Erfahrungen verfügt. Nach dem Einbau Ihres gewünschten Dachfensters sind wir selbstverständlich weiterhin Ihr Ansprechpartner. Die Betreuung unserer Bestandskunden ist ebenso wichtig für uns wie die Betreuung unsere Neukunden. Wir arbeiten stets lösungsorientiert und haben auch während des Einbaus ein offenes Ohr für Anregungen und Wünsche.

Gerade an Fenstern kann es bei Sonnenschein zu einer enormen Hitzeentwicklung kommen. Unsere Fenster-Markisen schaffen da Abhilfe und schützen vor ungewollten Blicken. Machen Sie Ihre Terrasse zu Ihrem ganz privaten Raum. Die weinor Vertikal-Beschattung VertiTex lässt auf Ihrer Terrasse eine ungestörte Atmosphäre entstehen. Neugierige Blicke bleiben einfach draußen, während das licht- und luftdurchlässige Tuch die Verbindung zu Natur und Garten schafft.

 Eleganter, senkrechter Sicht- und Sonnenschutz für Ihre Terrasse oder Ihre Fenster heißt bei uns VertiTex. Das System ist leicht nachrüstbar, kann sehr variabel und vielseitig eingesetzt werden und harmoniert hervorragend mit unseren WeiTop Dächern. Die modernen Soltis-Tücher schaffen eine angenehm geschützte, helle Atmosphäre – gleichzeitig können Sie Ihre Umgebung auch durch das Tuch hindurch erkennen. Design • 47 Gestellfarben/ 8 Wiga-Trend Farben - die weinor Farbvielfalt ist einzigartig. • Anspruchsvolle Dessins aus unseren exklusiven Tuchkollektionen • Kassetten-Design von klassisch bis modern Technik • max. Breite: 600 cm • max. Anlagenhöhe: 240 cm • Wand-, Decken- oder Dachsparrenmontage • Einfache Montage durch das Einhängen in die Dachrinne (bei WeiTop) oder als Wand- oder Deckenmontage. Alternativ auch auf den Fensterrahmen oder in die Fensterlaibung (bei VertiTex Universal) • Motorantrieb serienmäßig

Korrosions- und Frostschutzmittel für wassergekühlte Fahrzeugmotoren • geprüfte Qualität • ansprechendes, verkaufsförderndes Design • nitrit-, amin, phosphatfreies Kühlerfrostschutzmittel für alle Benzin- und Dieselmotoren • leicht verständliche Gebrauchsanweisungen mit Sicherheitsratschlägen auf einen Blick • ständige Qualitätskontrollen Artikelnummer: 8105000000 EAN: 4001068702024 Inhalt: 5000 ml Stück im Karton: 3 Karton/Palette: 48 Kanister/Palette: 144 Maße Kanister (L/B/H): 18 x 12 x 28 cm Maße Karton (L/B/H): 41 x 18,5 x 30 cm Maße Palette (L/B/H): 120 x 80 x 134 cm Gewicht Kanister: 5,88 kg Gewicht Karton: 17,88 kg Gewicht Palette: 882,24 kg

OECD 431 / In Vitro Skin Corrosion: Reconstructed Human Epidermis (RhE)Test Method Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com OECD 431: Skin Corrosion in the regulatory hazard classification and labeling context is defined as the production of irreversible damage to skin, generally evident as necrosis through the epidermis and into the dermis, following a defined chemical exposure. The In Vitro Skin Corrosion Test is an in vitro, non-animal test designed to identify those chemicals and mixtures capable of inducing skin corrosion (UN GHS Category 11), and in some cases to partially subcategorize corrosives into UN GHS Sub-Categories 1A or 1B and 1C (ie., the current test methods do not effectively discriminate between UN GHS Sub-Categories 1B and 1C). This test method is useful for regulatory classification and labeling of chemicals and mixtures, and depending upon the regulatory jurisdiction and framework the test results may be used as standalone or to support a weight of evidence approach. Since skin corrosion in vivo typically results from rapid chemical-induced cell damage, this test method provides a mechanistically-relevant measurement of cell viability in reconstructed human epidermis (RhE) tissues after a single topically-applied chemical treatment, relative to negative control-treated tissues. INVITRO-CONNECT has extensive expertise with a wide variety of reconstructed skin-based protocols. INVITRO-CONNECT staff members participated in the original validation study management that led to the adoption of the OECD Test Guideline 431: In Vitro Skin Corrosion: Reconstructed Human Epidermis Test Method (TG 431). NOTE: Since this test method does not discriminate among any non-corrosive categories, a non-corrosive prediction by this test method should be followed up with a test for potential skin irritation, using any of the validated Skin Irritation Test (SIT) methods, including the In Vitro Skin Irritation Test using a Reconstructed Human Epidermis (RhE) Model. A variety of other protocols are available to evaluate for potential skin irritation across a spectrum of irritation and corrosion responses to support product development, product stewardship, candidate formulation selection and other non-regulatory applications, and can provide a rank ordering of skin irritation potential. A variety of protocols allow for evaluation of mild formulations such as: Time-to-Toxicity ET50 Screening protocol Cytokine Expression Assay for Mild Products In Vitro Skin Irritation / Corrosion Screen for moderate to corrosive products and mixtures If full corrosive Sub-Categorization is essential and to discriminate between UN GHS Sub-Categories 1B and 1C, the Corrositex Membrane Barrier Time Monitor may be used. 3-D reconstructed human epidermis (RhE) models such as the EpiDerm™ (MatTek Corp.), epiCS® (CellSystems), LabCyte EPI-MODEL (Japan Tissue Engineering Co., Ltd. ), and EpiSkin™ and SkinEthic™ RHE (EpiSkin SA) are organotypic in vitro models of human epidermis which can be utilized in a variety of assays to evaluate the dermal irritation, corrosivity, cytotoxicity, phototoxicity, and/or anti inflammatory potential of test materials. Viability of the tissues is determined using the vital dye MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide). The reduction of MTT in test material-treated tissues is expressed as a percentage relative to negative control-treated cultures. The EpiDerm™, epiCS®, LabCyte EPI-MODEL, EpiSkin™ and SkinEthic™ RHE tissue models are made from human epithelial cells, which are cultured on specially designed cell culture inserts. The cells differentiate to form a fully differentiated epidermis, complete with a functional stratum corneum (see picture below). An advantage of using 3-D RhE tissues is that test materials are applied topically, at full formulation strength, without dilution, so that most forms of test materials can be applied to the cultures in the same manner as occurs in vivo. 1 United Nations (UN) Globally Harmonized System (GHS) of Classification and Labelling of Chemicals

Test Guideline No. 439 OECD 439 / in Vitro Skin Irritation Reconstructed Human Epidermis Test Method Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com OECD 439 / Skin Irritation Test (SIT) in a Reconstructed Human Epidermis (RhE) Model Skin Irritation in the regulatory hazard classification and labeling context is defined as the production of reversible damage to skin following a defined chemical exposure. The Skin Irritation Test (SIT) is an in vitro, non-animal test designed to identify those chemicals and mixtures capable of inducing moderate skin irritation (UN GHS Category 2 Skin Irritants1), and to discriminate UN GHS Category 2 Skin Irritants from UN GHS 3 Mild Skin Irritants as well as those not requiring classification for skin irritation potential. This test method is useful for regulatory classification and labeling of chemicals and mixtures, and depending upon the regulatory jurisdiction and framework the test results may be used as standalone or to support a weight of evidence approach. Since skin irritation in vivo typically results from chemical-induced cell damage and subsequent inflammatory cascade, this test method provides a mechanistically-relevant measurement of cell viability in reconstructed human epidermis (RhE) tissues after a single topically-applied chemical treatment, relative to negative control-treated tissues. Chemicals which reduce relative viability to ≤ 50% would be classified as an irritant (and a potential corrosive), while those which result in a relative viability > 50% would not be classified as a skin irritant in accordance with UN GHS Category 2. INVITRO-CONNECT GmbH has extensive expertise with a wide variety of reconstructed skin-based protocols and participated in the pre-validation and validation studies that led to the adoption of the OECD Test Guideline 439: In Vitro Skin Irritation: Reconstructed Human Epidermis Test Method (TG 439). NOTE: Since this test method does not discriminate UN GHS categories 1 and 2, an irritant prediction by this test method should be followed up with a test for potential skin corrosion, using any of the validated corrosivity test methods. 1) Corrositex Membrane Barrier Time Monitor Corrosion Test Method and 2) In Vitro Skin Corrosion Test using a Reconstructed Human Epidermis (RhE) Model A variety of other protocols are available to evaluate for potential skin irritation to support product development, product stewardship, candidate formulation selection and other non-regulatory applications, and can provide a rank ordering of skin irritation potential. A variety of protocols allow for evaluation of mild formulations: 1) Time-to-Toxicity ET50 Screening protocol, and 2) Cytokine Expression Assay for Mild Products and for moderate to corrosive products and mixtures: 3) In Vitro Skin Irritation / Corrosion Screen 3-D reconstructed human epidermis (RhE) models such as the EpiDerm™ (MatTek Corp.), epiCS® (CellSystems), LabCyte EPI-MODEL (Japan Tissue Engineering Co., Ltd. ), and EpiSkin™ and SkinEthic™ RHE (EpiSkin SA) are organotypic in vitro models of human epidermis which can be utilized in a variety of assays to evaluate the dermal irritation, corrosivity, cytotoxicity, phototoxicity, and/or anti inflammatory potential of test materials. Viability of the tissues is determined using the vital dye MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide). The reduction of MTT in test material-treated tissues is expressed as a percentage relative to negative control-treated cultures. The EpiDerm™, epiCS®, LabCyte EPI-MODEL, EpiSkin™ and SkinEthic™ RHE tissue models are made from human epithelial cells, which are cultured on specially designed cell culture inserts. The cells differentiate to form a fully differentiated epidermis, complete with a functional stratum corneum (see picture below). An advantage of using 3-D RhE tissues is that test materials are applied topically, at full formulation strength, without dilution, so that most forms of test materials can be applied to the cultures in the same manner as occurs in vivo. 1 United Nations (UN) Globally Harmonized System (GHS) of Classification and Labelling of Chemicals