Hai cercato: Cyclohexyl+methacrylate

Codice catalogo: (BOSSBS-15484R-A555)

Fornitore: Bioss

Codice articolo fornitore: BS-15484R-A555

Codice articolo locale: BOSSBS-15484R-A555

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.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15484R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-15484R-A680

Codice articolo locale: BOSSBS-15484R-A680

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.

UOM: 1 * 100 µl

Promo

Fornitore: TCI

Descrizione: 4'-Cyclohexylacetophenone ≥98.0% (by GC)

Codice catalogo: (TCIAC0920-25G)

Fornitore: TCI

Codice articolo fornitore: C0920-25G

Codice articolo locale: TCIAC0920-25G

Descrizione: Acido 2-(N-Cicloesilamino)etansolfonico (CHES) ≥99.0% (by titrimetric analysis) good's buffer component for biological research

UOM: 1 * 25 g

Promo

Fornitore: TCI

Descrizione: Hexythiazox ≥98.0% (by HPLC, total nitrogen)

Fornitore: Thermo Fisher Scientific

Descrizione: 4'-Cyclohexylacetophenone ≥99%

MSDS Certificati

Codice catalogo: (EHERCA14971740)

Fornitore: EHRENSTORFER

Codice articolo fornitore: CA14971740

Codice articolo locale: EHERCA14971740

Descrizione: Etil-metacrilato

UOM: 1 * 1 mL

Promo

Fornitore: TCI

Descrizione: Oxybutynin hydrochloride

Fornitore: TCI

Descrizione: Hexazinone ≥98.0% (by HPLC, titration analysis)

Codice catalogo: (BOSSBS-15484R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-15484R-CY3

Codice articolo locale: BOSSBS-15484R-CY3

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.

UOM: 1 * 100 µl

Promo

Codice catalogo: (APOSOR960946-25G)

Fornitore: Apollo Scientific

Codice articolo fornitore: OR960946-25G

Codice articolo locale: APOSOR960946-25G

Descrizione: Boc-Cha-OH 97%

UOM: 1 * 25 g

Promo

Fornitore: Avantor

Descrizione: Buffer for liquid chromatography and other molecular biology applications. Lot analysis on label.

MSDS Certificati

Fornitore: Apollo Scientific

Descrizione: 4'-Cyclohexylacetophenone 98%

Fornitore: Thermo Fisher Scientific

Descrizione: Dicyclohexylmethane-4,4'-diisocyanate (mixture of isomers) mixture of isomers 90% (mixture of isomers), AcroSeal®

MSDS

Fornitore: TCI

Descrizione: 1-Cyclohexylpiperazine ≥98.0% (by GC, titration analysis)

Fornitore: TCI

Descrizione: N-Ethylcyclohexylamine ≥99.0% (by GC)