Hai cercato: Alphazurine+A

Descrizione: 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.

Codice catalogo: BOSSBS-15484R-CY7

UOM: 1 * 100 µl

Codice articolo fornitore: BS-15484R-CY7

Codice articolo locale: BOSSBS-15484R-CY7

Fornitore: Bioss

Promo

Descrizione: Etil-metacrilato

Codice catalogo: EHERCA14971740

UOM: 1 * 1 mL

Codice articolo fornitore: CA14971740

Codice articolo locale: EHERCA14971740

Fornitore: EHRENSTORFER

Promo

Descrizione: 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.

Codice catalogo: BOSSBS-15484R-HRP

UOM: 1 * 100 µl

Codice articolo fornitore: BS-15484R-HRP

Codice articolo locale: BOSSBS-15484R-HRP

Fornitore: Bioss

Promo

Descrizione: Butilmetacrilato

Codice catalogo: EHERCA14971720

UOM: 1 * 1 mL

Codice articolo fornitore: CA14971720

Codice articolo locale: EHERCA14971720

Fornitore: EHRENSTORFER

Promo

Descrizione: 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.

Codice catalogo: BOSSBS-15484R-A350

UOM: 1 * 100 µl

Codice articolo fornitore: BS-15484R-A350

Codice articolo locale: BOSSBS-15484R-A350

Fornitore: Bioss

Promo

Descrizione: 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.

Codice catalogo: BOSSBS-15484R-A647

UOM: 1 * 100 µl

Codice articolo fornitore: BS-15484R-A647

Codice articolo locale: BOSSBS-15484R-A647

Fornitore: Bioss

Promo

Descrizione: 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.

Codice catalogo: BOSSBS-15484R-CY3

UOM: 1 * 100 µl

Codice articolo fornitore: BS-15484R-CY3

Codice articolo locale: BOSSBS-15484R-CY3

Fornitore: Bioss

Promo

Descrizione: 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.

Codice catalogo: BOSSBS-15484R-A488

UOM: 1 * 100 µl

Codice articolo fornitore: BS-15484R-A488

Codice articolo locale: BOSSBS-15484R-A488

Fornitore: Bioss

Promo

Descrizione: 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.

Codice catalogo: BOSSBS-15484R-A555

UOM: 1 * 100 µl

Codice articolo fornitore: BS-15484R-A555

Codice articolo locale: BOSSBS-15484R-A555

Fornitore: Bioss

Promo

Descrizione: 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.

Codice catalogo: BOSSBS-15484R-A680

UOM: 1 * 100 µl

Codice articolo fornitore: BS-15484R-A680

Codice articolo locale: BOSSBS-15484R-A680

Fornitore: Bioss

Promo

Descrizione: 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.

Codice catalogo: BOSSBS-15484R-A750

UOM: 1 * 100 µl

Codice articolo fornitore: BS-15484R-A750

Codice articolo locale: BOSSBS-15484R-A750

Fornitore: Bioss

Promo

Descrizione: Organic Standard, Metile metacrilato (monomero) 100 µg/ml in cicloesano, Tipo di conf.: bottiglia in vetro

Codice catalogo: EHERXA14971770CY

UOM: 1 * 1 mL

Codice articolo fornitore: XA14971770CY

Codice articolo locale: EHERXA14971770CY

Fornitore: EHRENSTORFER

Promo

Descrizione: Technovit 7100 is a plastic embedding system based on HEMA (2-hydroxyethyl methacrylate). The hydrophillic resin is used in medicine, botany, zoology and in the industry for embedding tissues for light microscope studies. The sections can be used for histological staining and enzyme detection.

Codice catalogo: HKUL64708991

UOM: 1 * 1 pezzi

Codice articolo fornitore: 64708991

Codice articolo locale: HKUL64708991

Fornitore: HERAEUS KULZER

Promo

Descrizione: N-Benzyl-N-methylaniline, Sigma-Aldrich®

Codice catalogo: 8.40106.0025

UOM: 1 * 25 mL

Codice articolo fornitore: 8.40106.0025

Codice articolo locale: MERC8.40106.0025

Fornitore: Merck

MSDS Promo

Descrizione: Benzyl propionate per sintesi, Sigma-Aldrich®

Codice catalogo: 8.43784.0500

UOM: 1 * 500 mL

Codice articolo fornitore: 8.43784.0500

Codice articolo locale: MERC8.43784.0500

Fornitore: Merck

MSDS Promo

Descrizione: Benzyl butyrate per sintesi, Sigma-Aldrich®

Codice catalogo: 8.16125.0500

UOM: 1 * 500 mL

Codice articolo fornitore: 8.16125.0500

Codice articolo locale: MERC8.16125.0500

Fornitore: Merck

MSDS Promo