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Image du produit-BOHLR649-55

b.safe Disc Sensor Holders

Numéro de catalogue: (BOHLR649-55)
Fournisseur: Bohlender
Description: <p>Made of PE, height-adjustable bracket for a b.safe disc sensor (catalogue number BOHLR640-05).</p>
UOM: 1 * 1 ST

New Product


Image du produit-ACRO211070010

Magnésium hydroxycarbonate léger (∼40,0 - 45,0% MgO) pour analyses

Fournisseur: Thermo Fisher Scientific
Description: Magnésium hydroxycarbonate léger (∼40,0 - 45,0% MgO) pour analyses

MSMD

Image non disponible-140000066.

FlashPure EcoFlex Amino Cartridges

Fournisseur: BUCHI
Description: FlashPure EcoFlex cartridge filled with spherical sorbent. FlashPure cartridges offered in a wide range of sizes, covering different stationary phases, particle sizes and geometries.

Image non disponible-33333.36

Magnésium hydroxycarbonate tétrahydraté (∼40 - 43,5% MgO), Qualité Réactif

Fournisseur: Thermo Fisher Scientific
Description: Magnésium hydroxycarbonate tétrahydraté (∼40 - 43,5% MgO), Qualité Réactif

MSMD Certificats

Image non disponible-BOSSBS-13623R-CY5

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy5®)

Numéro de catalogue: (BOSSBS-13623R-CY5)
Fournisseur: Bioss
Description: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-13623R-CY3

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy3®)

Numéro de catalogue: (BOSSBS-13623R-CY3)
Fournisseur: Bioss
Description: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-13623R-A555

Anti-TMEM176A Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Numéro de catalogue: (BOSSBS-13623R-A555)
Fournisseur: Bioss
Description: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-13623R-CY7

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy7®)

Numéro de catalogue: (BOSSBS-13623R-CY7)
Fournisseur: Bioss
Description: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image non disponible-EHERC17883500

2,3,5-Triméthylphénol

Numéro de catalogue: (EHERC17883500)
Fournisseur: EHRENSTORFER
Description: 2,3,5-Triméthylphénol
UOM: 1 * 0,25 g
Image non disponible-BOSSBS-13623R-HRP

Anti-TMEM176A Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Numéro de catalogue: (BOSSBS-13623R-HRP)
Fournisseur: Bioss
Description: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-13623R-FITC

Anti-TMEM176A Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Numéro de catalogue: (BOSSBS-13623R-FITC)
Fournisseur: Bioss
Description: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-13623R-A488

Anti-TMEM176A Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Numéro de catalogue: (BOSSBS-13623R-A488)
Fournisseur: Bioss
Description: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image non disponible-PROOCIL-PCB-23-C

2,3,5-Trichlorobiphényle

Numéro de catalogue: (PROOCIL-PCB-23-C)
Fournisseur: LGC Standards PROMOCHEM
Description: 2,3,5-Trichlorobiphényle
UOM: 1 * 5 mg
Image non disponible-BOSSBS-13623R-A647

Anti-TMEM176A Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Numéro de catalogue: (BOSSBS-13623R-A647)
Fournisseur: Bioss
Description: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image non disponible-MOLE15131983-25G

2,3,5-Collidine

Numéro de catalogue: (MOLE15131983-25G)
Fournisseur: Molekula
Description: 2,3,5-Collidine
UOM: 1 * 25 g

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Image du produit-HIRS9222275

Capillaires, traités à l'héparine sodique (avec revêtement), pour gazométrie sanguine

Fournisseur: HIRSCHMANN
Description: Borosilicate glass 3.3.

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Le stock de cet article est limité mais peut être disponible dans un entrepôt proche de vous. Merci de vous assurer que vous êtes connecté sur le site afin que le stock disponible soit affiché. Si l'call est toujours affiché et vous avez besoin d'aide, s'il vous plaît appelez-nous au 016 385 011
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