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Monoclonal Antibody, ELISA Kit, Polyclonal Antibody, Recombinant/Purified Protein.
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Index / GenWay / Short chain 3-hydroxyacyl-CoA dehydrogenase. mitochondrial - EC 1.1.1.35; HCDH; Medium and short chain L-3-hydroxyacyl-coenzyme A dehydrogenase / Product Detail : 10-288-22261F Short chain 3-hydroxyacyl-CoA dehydrogenase. mitochondrial - EC 1.1.1.35; HCDH; Medium and short chain L-3-hydroxyacyl-coenzyme A dehydrogenase
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#10-288-22261F Short chain 3-hydroxyacyl-CoA dehydrogenase. mitochondrial - EC 1.1.1.35; HCDH; Medium and short chain L-3-hydroxyacyl-coenzyme A dehydrogenase
| Price : | 401 | EUR |
| 455 | USD | |
| 311 | GBP | |
| 1685 | Zloty | |
| 53677 | JPY | |
| 3093 | NOK | |
| 3315 | SEK | |
| 453 | CHF |
Product name : Short chain 3-hydroxyacyl-CoA dehydrogenase. mitochondrial - EC 1.1.1.35; HCDH; Medium and short chain L-3-hydroxyacyl-coenzyme A dehydrogenase
Catalog number : 10-288-22261F
Quantity: 0.1 mg
Availability: Yes
Supplier name : GenWay
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WP1614: 1- and 2-Methylnaphthalene degradation
WP1626: Benzoate degradation via CoA ligation
WP1633: Bisphenol A degradation
WP1647: Fatty acid biosynthesis
WP1654: gamma-Hexachlorocyclohexane degradation
WP1665: Limonene and pinene degradation
WP1673: Naphthalene and anthracene degradation
WP1708: Terpenoid backbone biosynthesis
WP1502: Mitochondrial biogenesis
WP1671: Methane metabolism
WP1711: Trinitrotoluene degradation
WP296: TCA Cycle - biocyc
WP1002: Electron Transport Chain
WP111: Electron Transport Chain
WP1119: Electron Transport Chain
WP1339: Electron Transport Chain
WP1493: Carbon assimilation C4 pathway
WP1566: Citrate cycle (TCA cycle)
WP1567: Glycolysis and Gluconeogenesis
WP1581: Histidine metabolism
WP1612: 1,2-Dichloroethane degradation
WP1615: 3-Chloroacrylic acid degradation
WP1621: Arginine and proline metabolism
WP1622: Ascorbate and aldarate metabolism
WP1627: Benzoate degradation via hydroxylation
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Bibliography :
[29425111] The safety of Lipistart, a medium-chain triglyceride based formula, in the dietary treatment of long-chain fatty acid disorders: a phase I study.
[28526709] Acetylation of mitochondrial proteins by GCN5L1 promotes enhanced fatty acid oxidation in the heart.
[28283530] Identification of enzymes involved in oxidation of phenylbutyrate.
[26950678] A novel HSD17B10 mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regression.
[26711077] [Study on the methylation of LCHAD gene promoter region in mitochondria of trophoblast cells incubated with long-chain fatty acids].
[26110041] A case report of short-chain acyl-CoA dehydrogenase deficiency (SCADD).
[25888220] Clinical outcome, biochemical and therapeutic follow-up in 14 Austrian patients with Long-Chain 3-Hydroxy Acyl CoA Dehydrogenase Deficiency (LCHADD).
[25111118] Genotype-based databases for variants causing rare diseases.
[24780638] Use of propofol for short duration procedures in children with long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiencies.
[23835545] When the usual symptoms become an unusual diagnosis: a case report of trifunctional protein complex.
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