Hai cercato: Dodecyl+methacrylate

Codice catalogo: (MDTC46-040-CI)

Fornitore: Corning

Codice articolo fornitore: 46-040-CI

Codice articolo locale: MDTC46-040-CI

Descrizione: Sodium Dodecyl Sulfate (SDS) is an anionic detergent with applications in SDS-PAGE protein analysis and nucleic acid purification. It is a wetting agent that is effective in both acid and alkaline solutions, and is most often used as a protein and lipid solubilization reagent. SDS is also a powerful protein denaturant. This 10% solution is prepared in 18 megaohm water and is 0.2µm filtered.

UOM: 1 * 1 pezzi

MSDS Certificati Promo

Fornitore: MP Biomedicals

Descrizione: SDS is an anionic detergent and wetting agent that is effective in both acid and alkaline solutions.
Used to solubilize and denature proteins for denaturing-PAGE. Most proteins bind SDS in a ratio of 1.4 g SDS per gram of protein. The charges intrinsic to the protein become insignificant compared to the overall negative charge provided by the bound SDS. The charge to mass ratio is essentially the same for each protein and will migrate in the gel based only on their size.

Fornitore: MP Biomedicals

Descrizione: SDS is an anionic detergent and wetting agent that is effective in both acid and alkaline solutions.

Codice catalogo: (BOSSBS-15484R-FITC)

Fornitore: Bioss

Codice articolo fornitore: BS-15484R-FITC

Codice articolo locale: BOSSBS-15484R-FITC

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: (EHERCA14971720)

Fornitore: EHRENSTORFER

Codice articolo fornitore: CA14971720

Codice articolo locale: EHERCA14971720

Descrizione: Butilmetacrilato

UOM: 1 * 1 mL

Promo

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

Codice catalogo: (EHERCA14971770)

Fornitore: EHRENSTORFER

Codice articolo fornitore: CA14971770

Codice articolo locale: EHERCA14971770

Descrizione: Metile metacrilato

UOM: 1 * 0,25 g

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

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: (EHERC13060400)

Fornitore: EHRENSTORFER

Codice articolo fornitore: C13060400

Codice articolo locale: EHERC13060400

Descrizione: Acido laurico

UOM: 1 * 0,25 g

Promo

Fornitore: G-Biosciences

Descrizione: Brij® 35

Fornitore: Honeywell Chemicals

Descrizione: ACS GENERAL USE SOLVENTS

MSDS Certificati

Codice catalogo: (EHERCA14971740)

Fornitore: EHRENSTORFER

Codice articolo fornitore: CA14971740

Codice articolo locale: EHERCA14971740

Descrizione: Etil-metacrilato

UOM: 1 * 1 mL

Promo

Fornitore: SIGMA ALDRICH MICROSCOPY

Descrizione: Brilliant Blue R (C.l. 42660) is a triaminotriarylmethane dye with two amino groups being benzylated and one phenylated. It is also known as brilliant indocyanine 6B and coomassie blue R250. Brilliant Blue R has been widely used for protein band detection after SDS-PAGE (sodium dodecyl sulfate-polyacrylamide gel electrophoresis).

Codice catalogo: (BOSSBS-15484R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-15484R-A350

Codice articolo locale: BOSSBS-15484R-A350

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