659 Results for: "Dodecyl+methacrylate"

Supplier: Apollo Scientific

Phosphoric Acid Dodecyl Ester-Diphenyl Ester 25g pack 1 * 25 g

Supplier: Apollo Scientific

4,7-Bis(5-Bromo-4-Dodecyl-2-Thienyl)-2,1,3-Benzothiadiazole 1g pack 1 * 1 g

Supplier: Apollo Scientific

4,7-Bis(5-Bromo-4-Dodecyl-2-Thienyl)-2,1,3-Benzothiadiazole 5g pack 1 * 5 g

Supplier: Thermo Fisher Scientific

Methacrylic acid, 99%, stab. with 100-250ppm hydroquinone or 4-methoxyphenol 1 * 2.000 g

Supplier: Apollo Scientific

Polyethylene Glycol Monomethyl Ether Methacrylate 500ml pack 1 * 500 mL

Supplier: SIGMA ALDRICH MICROSCOPY

Brilliant Blue G has been used for determining the urine protein concentration. It has been used for the protein band detection after SDS-PAGE (sodium dodecyl sulfate polyacrylamide gel electrophoresis). It has been used as a P2X7R (purinergic receptor) antagonist.

Supplier: Apollo Scientific

Polyethylene Glycol Monomethyl Ether Methacrylate 500ml pack 1 * 500 mL

Supplier: Apollo Scientific

Polyethylene Glycol Monomethyl Ether Methacrylate 100ml pack 1 * 100 mL

Supplier: Apollo Scientific

Octahydro-1H-4,7-methanoinden-5-yl methacrylate 100g pack 1 * 100 g

Supplier: Apollo Scientific

Polyethylene Glycol Monomethyl Ether Methacrylate 2.5kg pack 1 * 2,5 kg

Supplier: Avantor

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.

Supplier: USP

USP reference standard Amino Methacrylate Copolymer (100 mg) 1 * 100 mg

Supplier: Thermo Fisher Scientific

n-Butyl methacrylate, 99%, stab. with 15-20 ppm 4-methoxyphenol 1 * 180 kg

Supplier: Apollo Scientific

4,7-Bis(5-Bromo-4-Dodecyl-2-Thienyl)-2,1,3-Benzothiadiazole 250mg pack 1 * 250 mg

Supplier: SIGMA ALDRICH MICROSCOPY

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.

Supplier: SIGMA ALDRICH MICROSCOPY

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).

Supplier: Rockland Immunochemicals

SDS-PAGE, sodium dodecyl sulfate polyacrylamide gel electrophoresis, describes a technique widely used in biochemistry to separate proteins according to their electrophoretic mobility (a function of the length of a polypeptide chain and its charge) and no other physical feature. SDS is an anionic detergent applied to protein sample to linearise proteins and to impart a negative charge to linearised proteins.

Supplier: HERAEUS KULZER

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.

Supplier: USP

Methoxycyclohexanol methacrylic aldehyde (25 mg) ((E)-3-((1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl)-2-methylacrylaldehyde) 1 * 25 mg

Supplier: Restek

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).

Supplier: HAMILTON BONADUZ

PRP-X500 is a superficially porous polymeric anion exchange column designed for the separation, purification and isolation of proteins, peptides and DNA/RNA. The methacrylate polymeric coating of the PRP-X500 provides a more hydrophilic surface, preventing hydrophobic interaction sample losses.

Supplier: USP

Orlistat Open Ring Amide (25 mg) (N-Formyl-L-leucine(S)-1-[(2S,3S)-2-hydroxy-3-[1-phenyl-R-ethyl-carbomoyl]nonyl]-dodecyl ester) 1 * 25 mg

Supplier: SIGMA ALDRICH MICROSCOPY

Brilliant Blue R concentrate is a methanol based stain especially designed for staining protein in polyacrylamide but will also stain agarose gels. The stain contains methanol and acetic acid so gels do not require fixing prior to staining. Brilliant Blue R Concentrate has been used for protein band detection after nondenaturing gradient gel electrophoresis, isoelectric focussing and SDS-PAGE (sodium dodecyl sulfate polyacrylamide gel electrophoresis). For detection of protein bands following electrophoresis.

Supplier: G-Biosciences

The hybridisation buffers like Church & Gilbert’s, Denhardt solution, hybridisation denaturing solution, hybridisation neutralising solution, SSC, SSPE, TMAC Hyb solution and TNT Buffer are used in wide range of applications. Church & Gilbert’s Hybridization Buffer is prepared from molecular biology grade SDS (sodium dodecyl sulfate), monosodium phosphate (NaHPO₄), EDTA (ethylenediaminetetracetic acid) and bovine serum albumin (BSA) Fraction V using DNase, RNase and Protease-free water. It consists of 1mM EDTA, 1% BSA, 0,5M sodium phosphate monobasic, and 7% SDS (at a pH of 7,2).

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.