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Image du produit-HICH51207

Avantor® Allsep Anion, Anion Exchange HPLC Columns

Fournisseur: Avantor
Description: Allsep anion is a methacrylate based phase with quaternary ammonium functional groups, optimised for use with both suppressed and non-suppressed conductivity detection. They are recommended for applications involving inorganic anions, weak and strong acid ions, metal complexes and organic acids.

Image du produit-634-0675

VWR®, Cuves à usage unique

Fournisseur: VWR Collection
Description: Cuves à usage unique en polystyrène (PS) optique ou en polyméthacrylate de méthyle (PMMA), adaptées à la plupart des solvants polaires, des solutions acides et alcalines.

Certificats

Image non disponible-1265424.

Ethyl Acrylate and Methyl Methacrylate Copolymer Dispersion, Reference Standard

Numéro de catalogue: (1265424.)
Fournisseur: USP
Description: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
UOM: 1 * 1,5 g
Image non disponible-APOSPC4390-100G

2,2,3,3,4,4,4-Heptafluorobutane-1-ol 98%

Fournisseur: Apollo Scientific
Description: Intermediate for speciality coating systems; acrylate and methacrylate esters are available.

Image non disponible-1029910.

Ammonio Methacrylate Copolymer , Reference Standards

Fournisseur: USP
Description: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

Image non disponible-TCIAM1531-5G

4-Methacryloyloxy-2,2,6,6-tetramethylpiperidine-1-oxyl ≥98.0% (par GC, analyse par titration) radical libre

Fournisseur: TCI
Description: 4-Methacryloyloxy-2,2,6,6-tetramethylpiperidine-1-oxyl ≥98.0% (par GC, analyse par titration) radical libre

Image non disponible-O8639-4X500ML

Osteo-Bed Bone Embedding Solvent

Numéro de catalogue: (O8639-4X500ML)
Fournisseur: SIGMA ALDRICH MICROSCOPY
Description: For use with Osteo-bed bone embedding kit. Solvent for removal of plastic from sections prior to rehydration and staining. Most histochemical and immunohistochemistry staining protocols require the removal of methyl methacrylate (MMA) and rehydration of mounted sections for improved stain penetration and greater contrast.
UOM: 1 * 2.000 mL
Image non disponible-BOSSBS-15484R-FITC

Anti-HIBCH Rabbit Polyclonal Antibody (FITC)

Numéro de catalogue: (BOSSBS-15484R-FITC)
Fournisseur: Bioss
Description: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15484R-A647

Anti-HIBCH Rabbit Polyclonal Antibody (ALEXA FLUOR® 647)

Numéro de catalogue: (BOSSBS-15484R-A647)
Fournisseur: Bioss
Description: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15484R

Anti-HIBCH Rabbit Polyclonal Antibody

Numéro de catalogue: (BOSSBS-15484R)
Fournisseur: Bioss
Description: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localizing to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyzes HIBYL-CoA, a saline catabolite, and β-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of β-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterized by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15484R-CY7

Anti-HIBCH Rabbit Polyclonal Antibody (Cy7)

Numéro de catalogue: (BOSSBS-15484R-CY7)
Fournisseur: Bioss
Description: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15484R-CY5

Anti-HIBCH Rabbit Polyclonal Antibody (Cy5)

Numéro de catalogue: (BOSSBS-15484R-CY5)
Fournisseur: Bioss
Description: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15484R-A350

Anti-HIBCH Rabbit Polyclonal Antibody (ALEXA FLUOR® 350)

Numéro de catalogue: (BOSSBS-15484R-A350)
Fournisseur: Bioss
Description: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image non disponible-ROTH4233.1

Méthyle méthacrylate stabilisé

Numéro de catalogue: (ROTH4233.1)
Fournisseur: Roth Carl
Description: Méthyle méthacrylate stabilisé
UOM: 1 * 1 L

Source d'approvisionnement du marché Il s'agit d'un élément MarketSource. Des frais supplémentaires peuvent s'appliquer.

Image non disponible-SERA28739.01

Méthacrylate de 3-triméthoxysilylpropyle

Numéro de catalogue: (SERA28739.01)
Fournisseur: Serva
Description: Méthacrylate de 3-triméthoxysilylpropyle
UOM: 1 * 100 mL

Source d'approvisionnement du marché Il s'agit d'un élément MarketSource. Des frais supplémentaires peuvent s'appliquer.

Image non disponible-BOSSBS-15484R-CY3

Anti-HIBCH Rabbit Polyclonal Antibody (Cy3)

Numéro de catalogue: (BOSSBS-15484R-CY3)
Fournisseur: Bioss
Description: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
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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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