U heeft gezocht op: Monoethyl+fumarate+calcium+salt


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Leverancier: LGC Standards PROMOCHEM
Omschrijving: Organic Standard, 3-ethyl 5-methyl 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-6-methylpyridine-3,5-dicarboxylate fumarate

Catalogus nummer: (EDQMY0001657)
Leverancier: EDQM
Omschrijving: Organic Standard, Quetiapine fumarate
UOM: 1 * 50 mg


Leverancier: Roth Carl
Omschrijving: Fumaarzuur

Leverancier: Spectrum Chemical
Omschrijving: BSE/TSE statement (available upon request)
Allergen statement (available upon request)

Catalogus nummer: (PROOMM0386.12)
Leverancier: LGC Standards PROMOCHEM
Omschrijving: Organic Standard, 3-Ethyl 5-methyl 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-6-methylpyridine-3,5-dicarboxylate fumarate
UOM: 1 * 100 mg


Catalogus nummer: (EHERC13955500)
Leverancier: EHRENSTORFER
Omschrijving: Fumaarzuur
UOM: 1 * 0,25 g

Leverancier: MERCK PRODUCTION CHEMICALS
Omschrijving: Fumaarzuur NF, SAFC®
Leverancier: Thermo Fisher Scientific
Omschrijving: Thiabendazole, a metal chelator and helminth-specific fumarate reductase inhibitor, is used primarily as an anthelmintic to control infections by helminth organisms.
Catalogus nummer: (PRSI91-668)
Leverancier: ProSci Inc.
Omschrijving: Fumarylacetoacetase belongs to the FAH family. Fumarylacetoacetase is primary expressed in liver and kidney. It exists as a homodimer and catalyses the hydrolysis of 4-fumarylacetoacetate into fumarate and acetoacetate. Defects in Fumarylacetoacetase cause tyrosinemia type 1, which is congenital metabolism defect characterised by elevated levels of tyrosine in the blood and urine, and hepatorenal manifestations. Typical features include renal tubular injury, self-mutilation, hepatic necrosis, episodic weakness, and seizures.
UOM: 1 * 1 EA


Catalogus nummer: (PRSI91-204)
Leverancier: ProSci Inc.
Omschrijving: Fumarase is an enzyme that catalyze the reversible hydration/dehydration of fumarate to S-malate and is involved in the tricarboxylic acid or Krebs cycle. Fumarase exists in both form, cytosolic formand N-terminal extend mitochondrial form. The N-terminal extended form is targeted to the mitochondrion, where the removal of the extension is the same form as in the cytoplasm. Fumarase is thought to act as a tumour suppressor, which deficiency can lead to progressive encephalopathy, cerebral atrophy and development delay.
UOM: 1 * 1 EA


Catalogus nummer: (PRSI29-614)
Leverancier: ProSci Inc.
Omschrijving: ASL is a member of the lyase 1 family. The protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in its gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency.This gene encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described.
UOM: 1 * 1 EA


Leverancier: MP Biomedicals
Omschrijving: Succinic acid is a dicarboxylic acid that occurs in nature in such organisms as fungi and lichens. In eukaryotes, succiniate, the anion of succinic acid, is an intermediate in the citric acid cycle, being formed from succinyl CoA and being converted to fumarate. Bacteria and plants can produce succinate from acetate or acetyl CoA, in the glyoxylate cycle.

Catalogus nummer: (PRSI29-615)
Leverancier: ProSci Inc.
Omschrijving: ASL is a member of the lyase 1 family. The protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in its gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency.This gene encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described.
UOM: 1 * 1 EA


Catalogus nummer: (PRSI92-016)
Leverancier: ProSci Inc.
Omschrijving: 4-Hydroxyphenylpyruvate Dioxygenase (4HPPD) belongs to the 4HPPD family. 4HPPD is a key enzyme in the degradation of tyrosine, which catalyzes the second reaction in the catabolism of tyrosine the conversation of 4-hydroxyphenylpyruvate to homogentisate. 4HPPD exists in homodimer forms, which uses zinc as a cofactor to catalyze the third step in the conversion of L-phenylalanine to fumarate and acetoacetic acid. When the active 4HPPD enzyme concentration is low in the human body, it results in high levels of tyrosine concentration in the blood, which can cause mild mental retardation at birth, and degradation in vision as a patient grows older.
UOM: 1 * 1 EA


Catalogus nummer: (1.02410.0050)
Leverancier: Merck
Omschrijving: Calcium carbonate, Certipur®, Supelco®
UOM: 1 * 50 g

Leverancier: Merck
Omschrijving: Calcium fluoride
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