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W02 antibody

Manufactured by Merck Group
Sourced in United Kingdom, United States

W02-antibody is a laboratory reagent produced by Merck Group. It is a monoclonal antibody designed for use in various research and diagnostic applications. The core function of the W02-antibody is to specifically bind and detect target molecules or analytes in biological samples.

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2 protocols using w02 antibody

1

Western Blot Analysis of Alzheimer's Proteins

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Cells were lysed in lysis buffer (150 mM NaCl, 50 mM Tris/HCl pH 7.4, 2 mM EDTA, 0.1% NP-40, 0.1% Triton-X 100) containing protease inhibitor cocktail (Roche Diagnostics, Mannheim, Germany), adjusted to equal protein amount and loaded on 10–20% Tricine gels (Anamed Elektrophorese, Groß-Bieberau, Germany). Proteins were transferred onto nitrocellulose membranes (Whatman, Dassel, Germany). For Western blot analysis the following primary antibodies were used: anti-sAPPβ MBS492139 (MyBioSource, SanDiego, USA), anti-NEP ab951 (Abcam, Cambridge, UK) and W02-antibody (Millipore, Billerica, USA) for detection of sAPPα and immunoprecipitated Aβ as described earlier (Grimm et al., 2011b (link), 2015 (link)). Anti-rabbit W401 (Promega, Mannheim, Germany) and anti-mouse P0260 (Dako, Hamburg, Germany) were used as secondary antibodies. Proteins were detected by ECL-method (Perkin Elmer, Rodgau-Jügesheim, Germany), densitometric quantification was performed with Image Gauge V3.45 software.
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2

Quantitative Analysis of BACE1, Aβ, and sAPPβ

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Samples used for the WB experiments were adjusted to equal protein concentration in advance.
For the determination of BACE1, cell lysates were prepared by lysing cells in 150 mM NaCl, 50 mM Tris/HCl pH 7.4, 2 mM EDTA, 0.1% NP-40, 0.1% Triton-X 100. For the determination of total secreted Aβ level and sAPPβ conditioned media were used.
The following antibodies were used for WB analysis: W02 antibody (5 μg/mL; Millipore, Billerica, MA, USA), anti-sAPPβ: Mbs492139 (1:250; MyBioSource, San Diego, CA, USA), BACE1: ab2077 (1:1000; abcam, Cambridge, UK), anti-actin ab1801 (1:1000; abcam), anti-rabbit IgG HRP Conjugate W401B (1:5000; Promega, Mannheim, Germany) and anti-mouse P0260 (Dako, Hamburg, Germany).
Aβ levels were detected by performing immunoprecipitation of conditioned media before WB analysis. Therefore, 20 μL protein G-Sepharose and W02 antibody (5 μg/mL) were used.
Enhanced chemiluminescense (ECL)-method (Perkin Elmer, Rodgau-Jügesheim, Germany) was used to detect proteins. Densitometrically quantification was performed by using Image Gauge V3.45 software (Fujifilm, Düsseldorf, Germany).
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