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Catalogus nummer: (BOSSBS-8218R-A555)
Leverancier: Bioss
Omschrijving: 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


Catalogus nummer: (BOSSBS-8218R-A350)
Leverancier: Bioss
Omschrijving: 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


Catalogus nummer: (BOSSBS-9672R-A647)
Leverancier: Bioss
Omschrijving: 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 C18orf54 gene product has been provisionally designated C18orf54 pending further characterization.
UOM: 1 * 100 µl


Catalogus nummer: (BOSSBS-7740R-A750)
Leverancier: Bioss
Omschrijving: 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


Leverancier: VACUUBRAND
Omschrijving: PTFE vacuum hose is antistatic. The inner side of the PTFE hose is smooth for increased chemical resistance, reduced deposits, and high conductance.

Leverancier: Welch by Gardner Denver
Omschrijving: A specially fractionated oil for DuoSeal® belt-driven pumps is designed to ensure the highest vacuum performance. The oil is tested to high vacuum levels to meet rigid requirements for vapor pressure, vacuum level stability, and viscosity. DuoSeal® oil is famous for its quality and consistency.

Leverancier: Thermo Fisher Scientific
Omschrijving: These are high quality glass tubes designed for heated, acid-based, vacuum hydrolysis of proteins and peptides for amino acid analysis. It fits conveniently into reacti-block aluminium heating blocks.

Leverancier: M I MATERIALS
Omschrijving: These Apiezon greases are hydrocarbon based, silicone-free and highly resistant to creep, the undesirable phenomenon associated with silicone-based products.
Catalogus nummer: (DOWC23900246)
Leverancier: DOW CORNING
Omschrijving: Molykote® High-Vacuum grease features a stiff, non-melting silicone formula that helps to seal and lubricate chemical processing equipment. Suitable for use in a wide range of applications including sealing vacuum and pressure systems, it is also doubles as a lubricant for o-rings in binoculars and telescopes as it prevents fogging of delicate lenses.
UOM: 1 * 50 g

Catalogus nummer: (24492.136)
Leverancier: M I MATERIALS
Omschrijving: Apiezon N Grease exhibits extremely low vapour pressures at ambient temperatures, 6×10<sup>-10</sup> torr at 20 °C, which are further improved by reductions in temperature to the cryogenic region.
UOM: 1 * 25 g

Catalogus nummer: (BOSSBS-9676R-CY7)
Leverancier: Bioss
Omschrijving: 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


Catalogus nummer: (BOSSBS-9676R-CY3)
Leverancier: Bioss
Omschrijving: 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


Catalogus nummer: (BOSSBS-9676R-CY5.5)
Leverancier: Bioss
Omschrijving: 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


Catalogus nummer: (BOSSBS-9676R-CY5)
Leverancier: Bioss
Omschrijving: 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


Catalogus nummer: (BOSSBS-9676R-FITC)
Leverancier: Bioss
Omschrijving: 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


Catalogus nummer: (BOSSBS-9676R-A488)
Leverancier: Bioss
Omschrijving: 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


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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