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Image Unavailable-BOSSBS-9675R-A680

Anti-C18orf56 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Varenummer: (BOSSBS-9675R-A680)
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 C18orf56 gene product has been provisionally designated C18orf56 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7740R-A555

Anti-CFAP53 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Varenummer: (BOSSBS-7740R-A555)
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-A350

Anti-GAREM Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Varenummer: (BOSSBS-8218R-A350)
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-HRP

Anti-C18ORF54 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Varenummer: (BOSSBS-9672R-HRP)
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-A555

Anti-GAREM Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Varenummer: (BOSSBS-8218R-A555)
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-7740R-A750

Anti-CCDC11 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Varenummer: (BOSSBS-7740R-A750)
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-9672R-A647

Anti-C18ORF54 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Varenummer: (BOSSBS-9672R-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 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-THSASPD300DDAA-230

Savant™ SpeedVac™ SPD300DDAA Large Capacity Vacuum Concentrator Kit

Varenummer: (THSASPD300DDAA-230)
Leverandør: THERMO SAVANT
Beskrivelse: Thermo Scientific™ Savant™ SpeedVac™ SPD300DDA vacuum concentrator is a large-capacity vacuum concentrator with a modular design, ideal for drying aggressive organic solvents, strong acids, bases, and combinatorial chemistry solvents. It is capable of drying larger quantities of samples at one time and can support high-volume sample preparation needs.
UOM: 1 * 1 Items
Product Image-TIGV111403B

Industrial vacuum cleaner, 2D-25L (DT) MFS WT

Varenummer: (TIGV111403B)
Leverandør: TIGER-VAC
Beskrivelse: This high efficeincy vacuum cleaner has been designed for general cleanup for the food industry.
UOM: 1 * 1 Items
Product Image-467-0145

Desiccator cabinets, Lab Companion™, SP Bel-Art

Leverandør: Bel-Art Products, a Part of SP
Beskrivelse: These compact, high-quality vacuum desiccators with clear or amber (UV blocking) polycarbonate maintain a vacuum and stay gastight allowing reliable dry storage or experiments over extended periods.

Image Unavailable-BOSSBS-9676R-CY7

Anti-C18ORF8 Rabbit Polyclonal Antibody (Cy7®)

Varenummer: (BOSSBS-9676R-CY7)
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-CY3

Anti-C18ORF8 Rabbit Polyclonal Antibody (Cy3®)

Varenummer: (BOSSBS-9676R-CY3)
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-CY5.5

Anti-C18ORF8 Rabbit Polyclonal Antibody (Cy5.5®)

Varenummer: (BOSSBS-9676R-CY5.5)
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-CY5

Anti-C18ORF8 Rabbit Polyclonal Antibody (Cy5®)

Varenummer: (BOSSBS-9676R-CY5)
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
Product Image-531-1423

Oil-Free Vacuum Pump for Vacuum Concentrator

Varenummer: (531-1423)
Leverandør: THERMO SAVANT
Beskrivelse: LTOFP400-230 is a high-efficiency, low-temperature oven designed for precise thermal processing in industrial and laboratory settings. Operating at 230V, it features advanced temperature control for consistent and uniform heat distribution, ensuring reliable results. Its robust construction and user-friendly interface make it ideal for applications such as drying, curing, and thermal testing. The LTOFP400-230 combines performance, durability, and ease of use, making it a versatile tool for various thermal processing needs.
UOM: 1 * 1 Items
Image Unavailable-BOSSBS-4944R-A488

Anti-SETBP1 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Varenummer: (BOSSBS-4944R-A488)
Leverandør: Bioss
Beskrivelse: SETBP1 (SET binding protein 1), also known as SEB, is a 1,542 amino acid nuclear protein that contains three AT hook DNA-binding domains, one SKI homology region and a C-terminal SET-binding domain, which is followed by three PPLPPPPP repeats. SETBP1 may be involved in SET-related tumorigenesis and leukemogenesis by regulating the transforming activity of SKI in the nucleus or suppressing SET function. As a widely expressed protein, SETBP1 is encoded by a gene that maps to human chromosome 18, which 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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