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Codice catalogo: (HPLC0001-6484)
Fornitore: COLLECTION PREFIX HPLC
Codice articolo fornitore: 0001-6484
Codice articolo locale: HPLC0001-6484
Descrizione: The Systec® Stand-Alone Prep-Scale HPLC vacuum degassing systems is high-efficiency, in-line modules that remove dissolved gases from the mobile phase. Their unique design assures reliable continuous operation and the highest level of performance available without the need for helium sparging. Up to five solvent lines may be degassed simultaneously by one unit.
UOM: 1 * 1 pezzi


Fornitore: Mettler - Toledo
Descrizione: This conductivity measuring cell utilises the four- pole potentiometric method for measuring conductivity, which incorporates a series of four graphite poles embedded in the probe shaft. This design completely eliminates the polarisation, which frequently occurs with the two-plate amperometric method during measuring high conductivity solution.

Codice catalogo: (KGWA17380-NW16)
Fornitore: KGW
Codice articolo fornitore: 17380-NW16
Codice articolo locale: KGWA17380-NW16
Descrizione: Simple cold traps, which are also known as cold finger condensers, are used in conjunction with vacuum pumps and the condensation Produced from humidity or solvents these cold traps can be used for many different tasks. With glass vacuum flanges you are able to connect this cold trap directly to the metal flanges of a high vacuum pump.
Made from borosilicate glass 3.3, in compliance with DIN/ISO 3585.
UOM: 1 * 1 pezzi


Fornitore: VACUUBRAND
Descrizione: Compact, powerful pump gives ideal solution for continuous, oil-free pumping of corrosive gases and vapors with exceptional high pumping speed. Eight-cylinder NT pump features quiet operation with smooth, easy-to-clean surfaces.

Codice catalogo: (THSAVLP120-230)
Fornitore: THERMO SAVANT
Codice articolo fornitore: VLP120-230
Codice articolo locale: THSAVLP120-230
Descrizione: LTVLP120-230 is a high-efficiency, reliable ventilation system designed for medium to large spaces. Featuring advanced air purification technology, it ensures optimal air quality by filtering out pollutants and allergens. With a robust construction and energy-saving capabilities, it offers both durability and cost-effectiveness. The user-friendly interface and customisable settings make it easy to operate, catering to various environmental needs. Ideal for commercial and residential applications, the LTVLP120-230 is a top choice for maintaining a healthy and comfortable indoor environment.
UOM: 1 * 1 pezzi


Codice catalogo: (BOSSBS-8218R)
Fornitore: Bioss
Codice articolo fornitore: BS-8218R
Codice articolo locale: BOSSBS-8218R
Descrizione: Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The FAM59A gene product has been provisionally designated FAM59A pending further characterization.
UOM: 1 * 100 µl


Codice catalogo: (THSARVT450-230)
Fornitore: THERMO SAVANT
Codice articolo fornitore: RVT450-230
Codice articolo locale: THSARVT450-230
Descrizione: RVT450-230 is a robust and efficient rotary vane vacuum pump designed for a wide range of industrial applications. It offers a high pumping speed and ultimate vacuum performance, ensuring reliable and consistent operation. The pump features a durable construction with advanced materials, providing long-lasting service life and minimal maintenance requirements. It operates on a 230 V power supply, making it suitable for various international settings. Ideal for use in laboratories, manufacturing processes, and other demanding environments, the RVT450-230 is a versatile and dependable choice for your vacuum needs.
UOM: 1 * 1 pezzi


Fornitore: DWK Life Sciences
Descrizione: These vacuum microfiltration assemblies are manufactured from 33 expansion, low extractable borosilicate glass. The 47 mm vacuum microfiltration assembly is used for general filtration and is designed to handle up to 500 ml of sample liquids for the analysis of particulate or microbiological contamination. The 90 mm vacuum microfiltration assembly is designed for large sample volumes or samples with high particulate loads that would tend to clog a 47 mm diameter filter. The assembly with fritted glass support is used for general filtration.

Codice catalogo: (BOSSBS-9676R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-9676R-CY7
Codice articolo locale: BOSSBS-9676R-CY7
Descrizione: MIC1 is a 657 amino acid protein that contains one MIC1 domain and is encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-9676R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-9676R-CY3
Codice articolo locale: BOSSBS-9676R-CY3
Descrizione: MIC1 is a 657 amino acid protein that contains one MIC1 domain and is encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-9676R-CY5.5)
Fornitore: Bioss
Codice articolo fornitore: BS-9676R-CY5.5
Codice articolo locale: BOSSBS-9676R-CY5.5
Descrizione: MIC1 is a 657 amino acid protein that contains one MIC1 domain and is encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-9676R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-9676R-CY5
Codice articolo locale: BOSSBS-9676R-CY5
Descrizione: MIC1 is a 657 amino acid protein that contains one MIC1 domain and is encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-8218R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-8218R-A750
Codice articolo locale: BOSSBS-8218R-A750
Descrizione: Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The FAM59A gene product has been provisionally designated FAM59A pending further characterisation.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-9675R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-9675R-A647
Codice articolo locale: BOSSBS-9675R-A647
Descrizione: Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf56 gene product has been provisionally designated C18orf56 pending further characterization.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-8218R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-8218R-A488
Codice articolo locale: BOSSBS-8218R-A488
Descrizione: Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The FAM59A gene product has been provisionally designated FAM59A pending further characterization.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-7740R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-7740R-HRP
Codice articolo locale: BOSSBS-7740R-HRP
Descrizione: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
UOM: 1 * 100 µl


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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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