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Numéro de catalogue: (BOSSBS-15484R-HRP)
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


Numéro de catalogue: (EHERCA14971770)
Fournisseur: EHRENSTORFER
Description: Méthyle méthacrylate
UOM: 1 * 0,25 g


Numéro de catalogue: (BOSSBS-15484R-A750)
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


Numéro de catalogue: (BOSSBS-15484R-A555)
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


Numéro de catalogue: (BOSSBS-15484R-A488)
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


Numéro de catalogue: (BOSSBS-15484R-A680)
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


Numéro de catalogue: (EHERCA14971720)
Fournisseur: EHRENSTORFER
Description: Méthacrylate de butyle
UOM: 1 * 1 mL


Numéro de catalogue: (EHERCA14971740)
Fournisseur: EHRENSTORFER
Description: Méthacrylate d'éthyle
UOM: 1 * 1 mL


Fournisseur: MP Biomedicals
Description: Adhesive

Numéro de catalogue: (REST30299)
Fournisseur: Restek
Description: Organic Standard, Methyl methacrylate, 1 ml/ampoule
UOM: 1 * 1 ST


Numéro de catalogue: (WAPR80-2004-53)
Fournisseur: Biochrom
Description: Accessoire pour colorimètre Colourwave et Biowave, Disposable methacrylate cells, 10 mm pathlength, 2,5 ml
UOM: 1 * 100 ST


Fournisseur: SARSTEDT
Description: Cuvettes in poly(methyl methacrylate) (PMMA) or polystyrene (PS).

Fournisseur: SELECTA
Description: These racks are designed for use with methacrylate tank.

Numéro de catalogue: (REST30202)
Fournisseur: Restek
Description: Contains 1 ml each of these mixtures: 524 calibration mix #7A, 524 calibration mix #7B. calibration mix #7A contains Acetone (67-64-1), 2-Butanone (MEK) (78-93-3), 2-Hexanone (591-78-6), 4-Methyl-2-pentanone (MIBK) (108-10-1), Tetrahydrofuran (109-99-9); calibration mix #7B contains Acrylonitrile (107-13-1)
Allyl chloride (3-chloropropene) (107-05-1), Ethyl methacrylate (97-63-2), Methyl acrylate (96-33-3), Methyl methacrylate (80-62-6), Nitrobenzene (98-95-3), Pentachloroethane (76-01-7).
UOM: 1 * 1 ST


Numéro de catalogue: (REST30215)
Fournisseur: Restek
Description: Mix contains: Acrylonitrile (107-13-1); Ethyl methacrylate (97-63-2); Malononitrile (109-77-3); Methacrylonitrile (126-98-7); Methyl methacrylate (80-62-6); Propionitrile (107-12-0); Styrene (100-42-5).
UOM: 1 * 1 mL


Numéro de catalogue: (EHERXA14971770CY)
Fournisseur: EHRENSTORFER
Description: Organic Standard, Méthyle méthacrylate (monomère) 100 µg/ml en solution dans cyclohexane, Type de conditionnement: Flacon Verre
UOM: 1 * 1 mL


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