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Catalog Number: (26572.295)
Supplier: VWR Chemicals
Description: Lead(II,IV) oxide, red, TECHNICAL
UOM: 1 * 1 kg

Supplier: Thermo Scientific
Description: Lead(IV) oxide ≥99.995% (metals basis), Puratronic®

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Supplier: Thermo Scientific
Description: Lead(IV) oxide 97+%, Extra Pure
Supplier: Thermo Scientific
Description: Lead(IV) oxide ≥97.0% ACS
Supplier: Thermo Scientific
Description: Lead(II,IV) oxide 98%
Catalog Number: (14232.A1)
Supplier: Thermo Scientific
Description: Lead(II,IV) oxide ≥97% (metals basis)
UOM: 1 * 1 kg

Supplier: Thermo Scientific
Description: Lead titanate ≥99.5%
Supplier: Thermo Scientific
Description: Lead titanate ≥99.9% (metals basis)
Catalog Number: (SIAL11536-1KG)
Supplier: Merck
Description: Lead(II,IV) oxide, Sigma-Aldrich®
UOM: 1 * 1 kg


Catalog Number: (SIAL518131-10G)
Supplier: Merck
Description: Lead(IV) oxide, Sigma-Aldrich®
UOM: 1 * 10 g


Supplier: Merck
Description: Lead(II,IV) oxide, Sigma-Aldrich®

Catalog Number: (ROTH4479.1)
Supplier: Roth Carl
Description: Lead(IV) oxide
UOM: 1 * 100 g


Catalog Number: (BOSSBS-0076R-A680)
Supplier: Bioss
Description: Functions as a cell surface receptor and performs physiological functions on the surface of neurons relevant to neurite growth, neuronal adhesion and axonogenesis. Involved in cell mobility and transcription regulation through protein-protein interactions. Can promote transcription activation through binding to APBB1-KAT5 and inhibits Notch signaling through interaction with Numb. Couples to apoptosis-inducing pathways such as those mediated by G(O) and JIP. Inhibits G(o) alpha ATPase activity (By similarity). Acts as a kinesin I membrane receptor, mediating the axonal transport of beta-secretase and presenilin 1. Involved in copper homeostasis/oxidative stress through copper ion reduction. In vitro, copper-metallated APP induces neuronal death directly or is potentiated through Cu(2+)-mediated low-density lipoprotein oxidation. Can regulate neurite outgrowth through binding to components of the extracellular matrix such as heparin and collagen I and IV. The splice isoforms that contain the BPTI domain possess protease inhibitor activity. Induces a AGER-dependent pathway that involves activation of p38 MAPK, resulting in internalisation of amyloid-beta peptide and leading to mitochondrial dysfunction in cultured cortical neurons. Provides Cu(2+) ions for GPC1 which are required for release of nitric oxide (NO) and subsequent degradation of the heparan sulfate chains on GPC1. Beta-amyloid peptides are lipophilic metal chelators with metal-reducing activity. Bind transient metals such as copper, zinc and iron. In vitro, can reduce Cu(2+) and Fe(3+) to Cu(+) and Fe(2+), respectively. Beta-amyloid 42 is a more effective reductant than beta-amyloid 40. Beta-amyloid peptides bind to lipoproteins and apolipoproteins E and J in the CSF and to HDL particles in plasma, inhibiting metal-catalysed oxidation of lipoproteins. Beta-APP42 may activate mononuclear phagocytes in the brain and elicit inflammatory responses.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-0076R-A750)
Supplier: Bioss
Description: Functions as a cell surface receptor and performs physiological functions on the surface of neurons relevant to neurite growth, neuronal adhesion and axonogenesis. Involved in cell mobility and transcription regulation through protein-protein interactions. Can promote transcription activation through binding to APBB1-KAT5 and inhibits Notch signaling through interaction with Numb. Couples to apoptosis-inducing pathways such as those mediated by G(O) and JIP. Inhibits G(o) alpha ATPase activity (By similarity). Acts as a kinesin I membrane receptor, mediating the axonal transport of beta-secretase and presenilin 1. Involved in copper homeostasis/oxidative stress through copper ion reduction. In vitro, copper-metallated APP induces neuronal death directly or is potentiated through Cu(2+)-mediated low-density lipoprotein oxidation. Can regulate neurite outgrowth through binding to components of the extracellular matrix such as heparin and collagen I and IV. The splice isoforms that contain the BPTI domain possess protease inhibitor activity. Induces a AGER-dependent pathway that involves activation of p38 MAPK, resulting in internalisation of amyloid-beta peptide and leading to mitochondrial dysfunction in cultured cortical neurons. Provides Cu(2+) ions for GPC1 which are required for release of nitric oxide (NO) and subsequent degradation of the heparan sulfate chains on GPC1. Beta-amyloid peptides are lipophilic metal chelators with metal-reducing activity. Bind transient metals such as copper, zinc and iron. In vitro, can reduce Cu(2+) and Fe(3+) to Cu(+) and Fe(2+), respectively. Beta-amyloid 42 is a more effective reductant than beta-amyloid 40. Beta-amyloid peptides bind to lipoproteins and apolipoproteins E and J in the CSF and to HDL particles in plasma, inhibiting metal-catalysed oxidation of lipoproteins. Beta-APP42 may activate mononuclear phagocytes in the brain and elicit inflammatory responses.
UOM: 1 * 100 µl


Catalog Number: (SIAL215805-250G)
Supplier: Merck
Description: Lead titanate, Sigma-Aldrich®
UOM: 1 * 250 g


Catalog Number: (13070.04)
Supplier: Thermo Scientific
Description: Lead(IV) fluoride ≥99%
UOM: 1 * 2 g

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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.
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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