3502 Results for: "3,5-Difluoropicolinic+acid&pageNo=59"

VWR®, Koelend thermoschudapparaat, Cooling Thermal Shake Touch

Supplier: VWR Collection

De Cooling Thermal Shake Touch, ontworpen voor toepassingen waarbij consistente en nauwkeurige resultaten vereist zijn. Het apparaat met laag profiel beschikt over verwarming, koeling en schudmogelijkheden, en maakt gebruik van verwisselbare blokken voor uiteenlopende buisjes en microplaten. Het LCD-aanraakscherm zorgt ervoor dat temperatuur, snelheid en tijd sneller kunnen worden ingesteld en deze waarden allemaal in één keer kunnen worden bekeken. Het display omvat Help-onderwerpen met bedieningstips. Het aanraakscherm is compatibel met rubberen handschoenen die in laboratoria worden gebruikt.

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MSC-Advantage™ Microbiologische veiligheidskast, Klasse II

Supplier: Thermo Scientific

Deze biologische veiligheidskast combineert een slim ontwerp en een buitengewone waarde met de beste energiezuinigheid, betrouwbaarheid en bruikbaarheid. Het geavanceerde ontwerp van de MSC-Advantage biologische veiligheidskast verbetert de complete werking en het onderhoud, waarborgt maximale veiligheid en optimaliseert het onderhoud en de reiniging. Met geavanceerde interne luchtstroom- en motortechnologie bieden MSC-Advantage kasten optimale energiezuinigheid, bediening en bruikbaarheid. Op volle snelheid verbruiken de motoren 60% minder energie dan standaardkasten. Om meer energie te besparen verlaagt de intelligente snelheidsregeling automatisch de ventilatorsnelheid naar 30% als het raam wordt gesloten. Deze technologie verhoogt de levensduur van de HEPA-filter, garandeert een steriele werkomgeving en bespaart energie om de operationele kosten te minimaliseren.

Sustainable Options Available

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Cubis® II MCA 225P ultrahoge resolutie semi-microbalansen

Supplier: Sartorius Balances

De Cubis® II laboratoriumbalansen zijn modulair, waardoor u kunt kiezen tussen toepassingen en configuraties die het beste bij uw behoeften passen. Deze balansen kunnen worden geconfigureerd op het niveau van display, windschermen, softwaretoepassingen en hardwarefuncties.

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Multi-parameter meters, handheld, HQ series

Supplier: Hach

Een robuuste en intuïtieve keuze aan draagbare meters, waarmee u vol vertrouwen uw resultaten kunt rapporteren en beheren.

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Anti-Amyloid beta-peptide Mouse Monoclonal Antibody [clone: MOAB-2]

Supplier: Biosensis

The amyloid beta peptide is derived from the cleavage of the Amyloid precursor protein (APP) and varies in length from 39 to 43 amino acids. However, the form(s) of amyloid-beta peptide (Aβ) associated with the pathology characteristic of Alzheimer’s disease (AD) remains unclear. In particular, the neurotoxicity of intraneuronal Aβ accumulation is an area of considerable research and controversy principally because antibodies thought to be specific for Aβ have been shown to actually detect intraneuronal APP and not Aβ exclusively. MOAB-2 (mouse IgG2b) is a pan-specific, high-titer antibody to Aβ residues 1-4 as demonstrated by biochemical and immunohistochemical analyses (IHC), and is highly specific just to amyloid beta peptide. MOAB-2 did not detect APP or APP-CTFs in cell culture media/lysates (HEK-APPSwe or HEK APPSwe/BACE1) or in brain homogenates from transgenic mice expressing 5 familial AD (FAD) mutation (5xFAD mice). Using IHC on 5xFAD brain tissue, MOAB-2 immunoreactivity co-localized with C-terminal antibodies specific for Aβ40 and Aβ42. MOAB-2 did not co-localize with either N- or C-terminal antibodies to APP. In addition, no MOAB-2-immunreactivity was observed in the brains of 5xFAD/BACE-/- mice, although significant amounts of APP were detected by N- and C-terminal antibodies to APP, as well as by 6E10. In both 5xFAD and 3xTg mouse brain tissue, MOAB-2 co-localized with cathepsin-D, a marker for acidic organelles, further evidence for intraneuronal Aβ, distinct from Aβ associated with the cell membrane. MOAB-2 demonstrated strong intraneuronal and extra-cellular immunoreactivity in 5xFAD and 3xTg mouse brain tissues.

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Anti-APP Mouse Monoclonal Antibody (Biotin) [clone: MOAB-2]

Supplier: Biosensis

The amyloid beta peptide is derived from the cleavage of the Amyloid precursor protein (APP) and varies in length from 39 to 43 amino acids. However, the form(s) of amyloid-beta peptide (Aβ) associated with the pathology characteristic of Alzheimer’s disease (AD) remains unclear. In particular, the neurotoxicity of intraneuronal Aβ accumulation is an area of considerable research and controversy principally because antibodies thought to be specific for Aβ have been shown to actually detect intraneuronal APP and not Aβ exclusively.

MOAB-2 (mouse IgG2b) is a pan-specific, high-titer antibody to Aβ residues 1-4 as demonstrated by biochemical and immunohistochemical analyses (IHC), and is highly specific just to amyloid beta peptide. MOAB-2 did not detect APP or APP-CTFs in cell culture media/lysates (HEK-APPSwe or HEK APPSwe/BACE1) or in brain homogenates from transgenic mice expressing 5 familial AD (FAD) mutation (5xFAD mice).

Using IHC on 5xFAD brain tissue, MOAB-2 immunoreactivity co-localized with C-terminal antibodies specific for Aβ40 and Aβ42. MOAB-2 did not co-localize with either N- or C-terminal antibodies to APP. In addition, no MOAB-2-immunreactivity was observed in the brains of 5xFAD/BACE-/- mice, although significant amounts of APP were detected by N- and C-terminal antibodies to APP, as well as by 6E10. In both 5xFAD and 3xTg mouse brain tissue, MOAB-2 co-localized with cathepsin-D, a marker for acidic organelles, further evidence for intraneuronal Aβ, distinct from Aβ associated with the cell membrane. MOAB-2 demonstrated strong intraneuronal and extra-cellular immunoreactivity in 5xFAD and 3xTg mouse brain tissues.

Biosensis now offers biotinylated MOAB-2 antibody allowing more flexibility in experimental design by using the biotin-avidin/streptavidin detection method. Biotinylated MOAB-2 antibody may also help to reduce background staining in difficult-to-stain tissues and increase detection sensitivity. The ability of biotinylated MOAB-2 antibody to detect amyloid beta has been validated by IHC.