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Catalog Number: (PRSI91-204)
Supplier: ProSci Inc.
Description: 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 * 50 µG


Catalog Number: (PRSI29-614)
Supplier: ProSci Inc.
Description: 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 * 50 µG


Catalog Number: (PRSI29-615)
Supplier: ProSci Inc.
Description: 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 * 100 µG


Supplier: Apollo Scientific
Description: t-Butyl methyl fumarate 97%

Supplier: Thermo Fisher Scientific
Description: Iron(II) fumarate 94%
Supplier: Thermo Fisher Scientific
Description: Potassium ethyl malonate 98%
Catalog Number: (APOSPC450077-250MG)
Supplier: Apollo Scientific
Description: [(1R)-1-(2-Fluorophenyl)ethyl][(1S)-1-phenylethyl]ammonium fumarate
UOM: 1 * 250 mg


Supplier: Thermo Fisher Scientific
Description: 2-Ethoxyethanol 99%, Extra Pure
Catalog Number: (1193301.)
Supplier: USP
Description: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. 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 mL


Supplier: Apollo Scientific
Description: (S)-(-)-2-(Boc-aminomethyl)-4,4-diethoxypiperidine fumarate

Catalog Number: (PRSI92-016)
Supplier: ProSci Inc.
Description: 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 * 50 µG


Catalog Number: (APOSPC450047-250MG)
Supplier: Apollo Scientific
Description: [(1R)-1-(3,5-Difluorophenyl)ethyl][(1S)-1-phenylethyl]ammonium fumarate
UOM: 1 * 250 mg


Catalog Number: (APOSOR200018-1G)
Supplier: Apollo Scientific
Description: 1-tert-Butyl 3-ethyl 3-phenylpiperidine-1,3-dicarboxylate fumarate 90%
UOM: 1 * 1 g


Catalog Number: (APOSPC450033-250MG)
Supplier: Apollo Scientific
Description: [(1R)-1-(3,5-Bis(Trifluoromethyl)phenyl)ethyl][(1S)-1-phenylethyl]ammonium fumarate
UOM: 1 * 250 mg


Catalog Number: (BOSSBS-3938R-A680)
Supplier: Bioss
Description: Defects in FH are the cause of fumarase deficiency (FHD)also known as fumaricaciduria. FHD is characterised by progressive encephalopathy, developmental delay, hypotonia, cerebral atrophy and lactic and pyruvic acidemia.
UOM: 1 * 100 µl


Catalog Number: (1592704.)
Supplier: USP
Description: 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 * 200 mg


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at +43 1 97002 - 0.
Dual use goods can only be delivered within the European Union.
Dual use goods can only be delivered within the European Union.
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The original product is no longer available. The replacement shown is available.
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