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Image Unavailable-BOSSBS-8218R-A350

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

Codice catalogo: (BOSSBS-8218R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-8218R-A350
Codice articolo locale: BOSSBS-8218R-A350
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
Image Unavailable-BOSSBS-8218R-A555

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

Codice catalogo: (BOSSBS-8218R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-8218R-A555
Codice articolo locale: BOSSBS-8218R-A555
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
Image Unavailable-BOSSBS-7740R-A750

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

Codice catalogo: (BOSSBS-7740R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-7740R-A750
Codice articolo locale: BOSSBS-7740R-A750
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
Product Image-531-1423

Oil-Free Vacuum Pump for Vacuum Concentrator

Codice catalogo: (531-1423)
Fornitore: THERMO SAVANT
Codice articolo fornitore: OFP400-230
Codice articolo locale: THSAOFP400-230
Descrizione: 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 pezzi
Image Unavailable-BOSSBS-9675R-A488

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

Codice catalogo: (BOSSBS-9675R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-9675R-A488
Codice articolo locale: BOSSBS-9675R-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 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-9675R-A350

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

Codice catalogo: (BOSSBS-9675R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-9675R-A350
Codice articolo locale: BOSSBS-9675R-A350
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
Product Image-WITG5.662.004

Stopcocks for desiccators

Codice catalogo: (WITG5.662.004)
Fornitore: witeg Labortechnik
Codice articolo fornitore: 5.662.004
Codice articolo locale: WITG5.662.004
Descrizione: Stopcock, with FCH-V 24/29, flat-free high vacuum joint, made of borosilicate glass.
UOM: 1 * 1 pezzi
Image Unavailable-BOSSBS-9672R-A488

Anti-C18ORF54 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Codice catalogo: (BOSSBS-9672R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-9672R-A488
Codice articolo locale: BOSSBS-9672R-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 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-HRP

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

Codice catalogo: (BOSSBS-8218R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-8218R-HRP
Codice articolo locale: BOSSBS-8218R-HRP
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
Image Unavailable-BOSSBS-8218R-FITC

Anti-GAREM Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Codice catalogo: (BOSSBS-8218R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-8218R-FITC
Codice articolo locale: BOSSBS-8218R-FITC
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
Image Unavailable-BOSSBS-7740R-A488

Anti-CFAP53 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Codice catalogo: (BOSSBS-7740R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-7740R-A488
Codice articolo locale: BOSSBS-7740R-A488
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
Image Unavailable-BOSSBS-8218R-CY5.5

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

Codice catalogo: (BOSSBS-8218R-CY5.5)
Fornitore: Bioss
Codice articolo fornitore: BS-8218R-CY5.5
Codice articolo locale: BOSSBS-8218R-CY5.5
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
Image Unavailable-BOSSBS-7740R-CY5.5

Anti-CFAP53 Rabbit Polyclonal Antibody (Cy5.5®)

Codice catalogo: (BOSSBS-7740R-CY5.5)
Fornitore: Bioss
Codice articolo fornitore: BS-7740R-CY5.5
Codice articolo locale: BOSSBS-7740R-CY5.5
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
Image Unavailable-BOSSBS-9675R-CY7

Anti-TYMSOS Rabbit Polyclonal Antibody (Cy7®)

Codice catalogo: (BOSSBS-9675R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-9675R-CY7
Codice articolo locale: BOSSBS-9675R-CY7
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
Image Unavailable-BOSSBS-9675R-CY5

Anti-TYMSOS Rabbit Polyclonal Antibody (Cy5®)

Codice catalogo: (BOSSBS-9675R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-9675R-CY5
Codice articolo locale: BOSSBS-9675R-CY5
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
Image Unavailable-BOSSBS-9672R-A350

Anti-C18ORF54 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Codice catalogo: (BOSSBS-9672R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-9672R-A350
Codice articolo locale: BOSSBS-9672R-A350
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 C18orf54 gene product has been provisionally designated C18orf54 pending further characterization.
UOM: 1 * 100 µl
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