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Image Unavailable-OXOIPB5080A

Culture media, ready to use, in plates

Varenummer: (OXOIPB5080A)
Leverandør: THERMO FISHER DIAGNOSTICS
Beskrivelse: Edwards agar modified, Plate, Størrelse: 90 mm, Standard: -, Ansøgning: Streptococci
UOM: 1 * 10 Items
Image Unavailable-REVCTSX60086FA

Universal General Purpose Ultra-Low Freezers, TSX

Leverandør: REVCO TECHNOLOGIES
Beskrivelse: The TSX Universal heralds a new era in performance with Universal V-Drive technology, delivering tighter control and faster recovery times. Coupled with an expanded setpoint range, universal voltage, whisper-quiet operation, simplified software updates and much more, TSX Universal seamlessly adapts to your workflow.

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Image Unavailable-BOSSBS-9672R-CY5

Anti-C18ORF54 Rabbit Polyclonal Antibody (Cy5®)

Varenummer: (BOSSBS-9672R-CY5)
Leverandør: Bioss
Beskrivelse: 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
Image Unavailable-BOSSBS-8218R-A647

Anti-GAREM Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Varenummer: (BOSSBS-8218R-A647)
Leverandør: Bioss
Beskrivelse: 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
Image Unavailable-ILMV700113

High vacuum through valves, VS series

Leverandør: Welch by Gardner Denver
Beskrivelse: These high vacuum through valves feature a very long life bellows-seal made from stainless steel.

Product Image-BIBBSSV104

Stopcocks, high vacuum

Leverandør: SciLabware
Beskrivelse: Borosilicate glass stopcocks specially designed for high vacuum applications.

Image Unavailable-THSAVLP285-230

Vacuum pumps, deep vacuum, oil

Leverandør: THERMO SAVANT
Beskrivelse: Deep vacuum oil pump is designed to work with SpeedVac applications.

Product Image-VACU20664006

High vacuum bellow valves, VE series

Leverandør: VACUUBRAND
Beskrivelse: High vacuum, helium leak-tested right angle valves VE have stainless steel bellows which seals the drive mechanism without any gap on the vacuum side.

Image Unavailable-BOSSBS-9676R-A647

Anti-C18ORF8 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Varenummer: (BOSSBS-9676R-A647)
Leverandør: Bioss
Beskrivelse: 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
Image Unavailable-BOSSBS-9676R-HRP

Anti-C18ORF8 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Varenummer: (BOSSBS-9676R-HRP)
Leverandør: Bioss
Beskrivelse: 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
Image Unavailable-BOSSBS-9675R

Anti-C18orf56 Rabbit Polyclonal Antibody

Varenummer: (BOSSBS-9675R)
Leverandør: Bioss
Beskrivelse: 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
Image Unavailable-BOSSBS-9672R

Anti-LAS2 Rabbit Polyclonal Antibody

Varenummer: (BOSSBS-9672R)
Leverandør: Bioss
Beskrivelse: 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
Image Unavailable-BOSSBS-8218R-CY3

Anti-GAREM Rabbit Polyclonal Antibody (Cy3®)

Varenummer: (BOSSBS-8218R-CY3)
Leverandør: Bioss
Beskrivelse: 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
Image Unavailable-BOSSBS-9672R-CY7

Anti-C18ORF54 Rabbit Polyclonal Antibody (Cy7®)

Varenummer: (BOSSBS-9672R-CY7)
Leverandør: Bioss
Beskrivelse: 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
Image Unavailable-BOSSBS-7740R-CY3

Anti-CFAP53 Rabbit Polyclonal Antibody (Cy3®)

Varenummer: (BOSSBS-7740R-CY3)
Leverandør: Bioss
Beskrivelse: 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
Image Unavailable-BOSSBS-8218R-CY7

Anti-GAREM Rabbit Polyclonal Antibody (Cy7®)

Varenummer: (BOSSBS-8218R-CY7)
Leverandør: Bioss
Beskrivelse: 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
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Lager for denne post er begrænset, men kan være til rådighed på et lager tæt på dig. Sørg for, at du er logget ind på webstedet, så tilgængelige bestand kan vises. Hvis call vises stadig, og du har brug for hjælp, bedes du ringe til os på - 43 86 87 88.
Dette produkt er mærket som begrænset og kan kun købes af godkendte Shipping konti. Hvis du har brug for yderligere hjælp, e-mail VWR Regulatory Department på Regulatory_Affairs@vwr.com
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Dette produkt er blevet blokeret for salg via hjemmesiden. Kontakt kundeservice for mere information.
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Produkt (er) markeret med dette symbol er udgået - sælges indtil lageret er tomt. Alternativer kan være tilgængelige ved at søge med VWR-katalognummeret ovenfor. Hvis du har brug for yderligere hjælp, bedes du kontakte kundeservice på telefon 4386 8788
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