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Image Unavailable-BOSSBS-7740R-A680

Anti-CCDC11 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalogus nummer: (BOSSBS-7740R-A680)
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
Image Unavailable-BOSSBS-9672R-CY5

Anti-C18ORF54 Rabbit Polyclonal Antibody (Cy5®)

Catalogus nummer: (BOSSBS-9672R-CY5)
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
Image Unavailable-BOSSBS-8218R-A647

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

Catalogus nummer: (BOSSBS-8218R-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 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
Product Image-181-0310

VWR® VP 220, Chemische, hoogwaardige membraanpomp

Catalogus nummer: (181-0310)
Leverancier: VWR Collection
Omschrijving: De VP 220 is ideaal voor rotatieverdampers die het krachtige vacuüm leveren dat nodig is voor veeleisende verdampingen zonder het gebruik van oliepompen. De VP 220 heeft ingebouwd Advanced Vapor Management (AVM), wat nauwkeurige controlemogelijkheden betekent voor de destillatie van organische oplosmiddelen en toepassingen waarbij agressieve dampen en gassen worden verwerkt. De VP 220 is vooral effectief voor rotatieverdamping van oplosmiddelen met een laag kookpunt, zoals aceton en ethanol, en kan DMF snel strippen bij 35 °C. De pomponderdelen zijn allemaal gemaakt van corrosiebestendige materialen zoals PTFE en Kalrez om agressieve dampen te kunnen verwerken, en samen met vacuümaanpassing wordt het verdampingsproces geoptimaliseerd. Gebruik de vacuümaanpassing om het vacuüm te verhogen totdat zich belletjes vormen in de verdampingskolf - en verlaag het vervolgens iets. Verlaag het vacuüm voor een snelle reactie op stoten of schuimen.
UOM: 1 * 1 ST
Image Unavailable-METN52200241

Connector, VarioPin

Catalogus nummer: (METN52200241)
Leverancier: Mettler - Toledo
Omschrijving: This connector fits with shielded coaxial cables (standard and high temperature).
UOM: 1 * 1 ST
Image Unavailable-OXOIPB5080A

Culture media, ready to use, in plates

Catalogus nummer: (OXOIPB5080A)
Leverancier: THERMO FISHER DIAGNOSTICS
Omschrijving: Edwards agar modified, Plate, Maat: 90 mm, Standaard: -,: Applicatie: Streptococci
UOM: 1 * 10 ST
Image Unavailable-ILMV700113

High vacuum through valves, VS series

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

Image Unavailable-BOSSBS-9672R-CY7

Anti-C18ORF54 Rabbit Polyclonal Antibody (Cy7®)

Catalogus nummer: (BOSSBS-9672R-CY7)
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
Image Unavailable-BOSSBS-9675R

Anti-C18orf56 Rabbit Polyclonal Antibody

Catalogus nummer: (BOSSBS-9675R)
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 C18orf56 gene product has been provisionally designated C18orf56 pending further characterization.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9672R

Anti-LAS2 Rabbit Polyclonal Antibody

Catalogus nummer: (BOSSBS-9672R)
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
Image Unavailable-BOSSBS-8218R-CY3

Anti-GAREM Rabbit Polyclonal Antibody (Cy3®)

Catalogus nummer: (BOSSBS-8218R-CY3)
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
Image Unavailable-BOSSBS-7740R-CY3

Anti-CFAP53 Rabbit Polyclonal Antibody (Cy3®)

Catalogus nummer: (BOSSBS-7740R-CY3)
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
Image Unavailable-BOSSBS-8218R-CY7

Anti-GAREM Rabbit Polyclonal Antibody (Cy7®)

Catalogus nummer: (BOSSBS-8218R-CY7)
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
Image Unavailable-BOSSBS-9676R-HRP

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

Catalogus nummer: (BOSSBS-9676R-HRP)
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
Image Unavailable-BOSSBS-9676R-A647

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

Catalogus nummer: (BOSSBS-9676R-A647)
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
Image Unavailable-THSAVLP285-230

Vacuum pumps, deep vacuum, oil

Leverancier: THERMO SAVANT
Omschrijving: Deep vacuum oil pump is designed to work with SpeedVac applications.

Bel voor prijs
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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