You Searched For: Lead+(II)+oxide


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Supplier: Thermo Fisher Scientific
Description: Zinc oxide 99,9 Metals basis
Catalog Number: (BOSSBS-11734R-A488)
Supplier: Bioss
Description: Located in the mitochondrial inner membrane, mitochondrial complex I is the first and largest enzyme in the electron transport chain of oxidative phosphorylation. By oxidizing NADH that is produced in the Krebs cycle, this complex utilizes the two electrons to reduce ubiquinone to ubiquinol, thereby initiating the passage of electrons to successive complexes and ultimately leading to the reduction of oxygen to water. Mitochondrial complex I consists of over 40 subunits and is of considerable clinical interest since defects in any of the subunits can lead to various myopathies and neuropathies. As a subunit of mitochondrial complex I, NDUFS7 (NADH dehydrogenase [ubiquinone] iron-sulfur protein 7), also designated NADH-ubiquinone oxidoreductase 20 kDa subunit, is a 213 amino acid protein that is suggested to be required for catalytic activity. Defects in the gene encoding NDUFS7 are the cause of Leigh syndrome, a severe neurological disorder that is characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions.
UOM: 1 * 100 µl


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Catalog Number: (BOSSBS-11734R-A555)
Supplier: Bioss
Description: Located in the mitochondrial inner membrane, mitochondrial complex I is the first and largest enzyme in the electron transport chain of oxidative phosphorylation. By oxidizing NADH that is produced in the Krebs cycle, this complex utilizes the two electrons to reduce ubiquinone to ubiquinol, thereby initiating the passage of electrons to successive complexes and ultimately leading to the reduction of oxygen to water. Mitochondrial complex I consists of over 40 subunits and is of considerable clinical interest since defects in any of the subunits can lead to various myopathies and neuropathies. As a subunit of mitochondrial complex I, NDUFS7 (NADH dehydrogenase [ubiquinone] iron-sulfur protein 7), also designated NADH-ubiquinone oxidoreductase 20 kDa subunit, is a 213 amino acid protein that is suggested to be required for catalytic activity. Defects in the gene encoding NDUFS7 are the cause of Leigh syndrome, a severe neurological disorder that is characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions.
UOM: 1 * 100 µl


Catalog Number: (6906-02)
Supplier: Avantor
Description: Water, ULTREX® II, Ultrapure, J.T.Baker®
UOM: 1 * 1 L

Supplier: Thermo Fisher Scientific
Description: Copper(II) oxide 99,995 Metals basis, Puratronic®
Supplier: Thermo Fisher Scientific
Description: Mercury (II) oxide, red 99%
Supplier: Thermo Fisher Scientific
Description: Nickel (II) oxide, black Ni_76 (contains Ni2O3)
Supplier: Thermo Fisher Scientific
Description: Cadmium oxide 99,95 Metals basis
Catalog Number: (BOSSBS-5107R-HRP)
Supplier: Bioss
Description: Hydrolyzes the toxic metabolites of a variety of organophosphorus insecticides. Capable of hydrolyzing a broad spectrum of organophosphate substrates and lactones, and a number of aromatic carboxylic acid esters. Mediates an enzymatic protection of low density lipoproteins against oxidative modification and the consequent series of events leading to atheroma formation.
UOM: 1 * 100 µl


Supplier: Thermo Fisher Scientific
Description: Cobalt(II,III) oxide
Supplier: Thermo Fisher Scientific
Description: Iron(II,III) oxide 97%, powder_nano
Catalog Number: (BOSSBS-13186R-CY7)
Supplier: Bioss
Description: The Flavin containing monooxygenase family consists of five gene products, FMO1-5, that are major enzymatic oxidants involved in the metabolism of various therapeutics. Located in the liver, FMO3 is a hepatic microsomal enzyme that oxygenates soft nucleophiles such as secondary and tertiary amines. Through its N-oxygenase capabilities, FMO3 acts on a variety of xenobiotics to catalyze oxidative digestion. Defects in the FMO3 gene are the primary cause of trimethylaminuria (TMAuria), an inborn error of metabolism associated with a fishy body odor emitting from sweat, urine and breath. Genetic mutations in FMO3 lead to the N-oxidation of amino-trimethylamine derived from food products, thus producing the malodor associated with TMAuria.
UOM: 1 * 100 µl


Supplier: Apollo Scientific
Description: Zinc oxide 99,9%

Supplier: Thermo Fisher Scientific
Description: Manganese(II) titanium oxide 99,9 Metals basis
Supplier: Thermo Fisher Scientific
Description: Cobalt(II,III) oxide 99,7 Metals basis
Supplier: Thermo Fisher Scientific
Description: Iron(II,III) oxide 97 Metals basis
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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 on +353 1 88 22222.
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 on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service on +353 1 8822222.
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