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Catalog Number: (0494-25G)
Supplier: VWR Chemicals
Description: (±)-α-Lipoic acid, high purity
UOM: 1 * 25 g

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Catalog Number: (A4065.0005)
Supplier: PanReac AppliChem
Description: (±)-α-Lipoic acid
UOM: 1 * 5 g


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Supplier: Thermo Scientific
Description: (±)-α-Lipoic acid 98+%
Supplier: Cayman Chemical
Description: (±)-α-Lipoic acid

Supplier: Thermo Scientific
Description: (±)-α-Lipoic acid ≥98%
Catalog Number: (1368201.)
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 * 500 mg


Catalog Number: (PROOMM0127.00)
Supplier: LGC Standards PROMOCHEM
Description: (±)-α-Lipoic acid
UOM: 1 * 500 mg


Catalog Number: (MOLEM68359886)
Supplier: Molekula
Description: (±)-α-Lipoic acid
UOM: 1 * 25 g


Supplier: Merck
Description: (±)-α-Lipoic acid, Sigma-Aldrich®

Supplier: Merck
Description: (±)-α-Lipoic acid, Sigma-Aldrich®

Catalog Number: (VWRU75811-506)
Supplier: VWR Collection
Description: Alpha Lipoic Acid, USP Dietary Supplement.
UOM: 1 * 1 items

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Supplier: MP Biomedicals
Description: DL-Thioctic Acid is a hydrogen transferrin cofactor.

Catalog Number: (ABCAAB58724-50)
Supplier: Abcam
Description: Anti-Lipoic Acid Rabbit Polyclonal Antibody
UOM: 1 * 50 µl


Catalog Number: (PRSI30-449)
Supplier: ProSci Inc.
Description: The process of transferring lipoic acid to proteins is a two-step process. The first step is the activation of lipoic acid by lipoate-activating enzyme to form lipoyl-AMP. For the second step, LIPT1 transfers the lipoyl moiety to apoproteins.The process of transferring lipoic acid to proteins is a two-step process. The first step is the activation of lipoic acid by lipoate-activating enzyme to form lipoyl-AMP. For the second step, the protein encoded by this gene transfers the lipoyl moiety to apoproteins. Alternative splicing in the 5' UTR of this gene results in five transcript variants that encode the same protein.
UOM: 1 * 50 µG


Catalog Number: (PRSI30-437)
Supplier: ProSci Inc.
Description: LIAS belongs to the biotin and lipoic acid synthetases family. It localizes in mitochondrion and plays an important role in alpha- (+)-lipoic acid synthesis. It may also function in the sulfur insertion chemistry in lipoate biosynthesis.The protein encoded by this gene belongs to the biotin and lipoic acid synthetases family. It localizes in mitochondrion and plays an important role in alpha- (+)-lipoic acid synthesis. It may also function in the sulfur insertion chemistry in lipoate biosynthesis. Alternative splicing occurs at this locus and two transcript variants encoding distinct isoforms have been identified.
UOM: 1 * 50 µG


Catalog Number: (PRSI26-849)
Supplier: ProSci Inc.
Description: The enzyme system for cleavage of glycine (glycine cleavage system; EC 2.1.2.10), which is confined to the mitochondria, is composed of 4 protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). Glycine encephalopathy (GCE) may be due to a defect in any one of these enzymes.The enzyme system for cleavage of glycine (glycine cleavage system; EC 2.1.2.10), which is confined to the mitochondria, is composed of 4 protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase; MIM 238300), H protein (a lipoic acid-containing protein; MIM 238330), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase; MIM 238331). Glycine encephalopathy (GCE; MIM 605899) may be due to a defect in any one of these enzymes.
UOM: 1 * 50 µG


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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.
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.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at +43 1 97002 - 0.
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