Hai cercato: Gabbie per animali

Fornitore: USP

Descrizione: 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.

Fornitore: Thermo Fisher Scientific

Descrizione: Acido metacrilico 99.5% stabilizzato, extra puro

MSDS Certificati

Fornitore: TCI

Descrizione: Acido metacrilico ≥99.0% (by GC) stabilizzato

Fornitore: TCI

Descrizione: 1-(Acryloyloxy)-3-(methacryloyloxy)-2-propanol ≥80.0% (by GC) stabilizzato

Codice catalogo: (1265424.)

Fornitore: USP

Codice articolo fornitore: 1265424

Codice articolo locale: USPH1265424

Descrizione: 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

Promo

Fornitore: USP

Descrizione: 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.

Fornitore: TCI

Descrizione: 4-Methacryloyloxy-2,2,6,6-tetramethylpiperidine-1-oxyl ≥98.0% (by GC, titration analysis) free radical

Fornitore: Apollo Scientific

Descrizione: Intermediate for speciality coating systems; acrylate and methacrylate esters are available.

Fornitore: VWR Collection

Descrizione: Cuvette monouso in polistirene ottico (PS) o polimetilmetacrilato (PMMA), per l'uso con la maggior parte dei solventi polari, acidi e soluzioni alcaline.

Fornitore: Avantor

Descrizione: 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.

Fornitore: TCI

Descrizione: 2-[2-Hydroxy-5-[2-(methacryloyloxy)ethyl]phenyl]-2H-benzotriazole ≥98.0% (by GC)

Codice catalogo: (O8639-4X500ML)

Fornitore: SIGMA ALDRICH MICROSCOPY

Codice articolo fornitore: O8639-4X500ML

Codice articolo locale: SIAMO8639-4X500ML

Descrizione: 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

Promo

Fornitore: MP Biomedicals

Descrizione: Adhesive

Codice catalogo: (BOSSBS-15484R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-15484R-CY7

Codice articolo locale: BOSSBS-15484R-CY7

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-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-15484R-CY5

Codice articolo locale: BOSSBS-15484R-CY5

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)

Fornitore: Bioss

Codice articolo fornitore: BS-15484R

Codice articolo locale: BOSSBS-15484R

Descrizione: 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

Promo