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Novex alkaline phosphatase conjugated goat anti rabbit or goat anti mouse immunoglobulin g igg secondary antibody

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Novex alkaline-phosphatase conjugated (goat) anti-rabbit or (goat) anti-mouse immunoglobulin G (IgG) secondary antibody is a laboratory reagent used to detect the presence of rabbit or mouse primary antibodies in various immunoassay techniques. The secondary antibody is conjugated with the enzyme alkaline phosphatase, which catalyzes a colorimetric reaction upon the addition of a suitable substrate, allowing for the visual detection and quantification of the target primary antibody.

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2 protocols using novex alkaline phosphatase conjugated goat anti rabbit or goat anti mouse immunoglobulin g igg secondary antibody

1

Elental Modulates FGF2 Protein Levels

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Cells (2.0 × 106 cells in 100 mm dish) were treated with different concentrations of Elental (0, 0.1, 0.5, 1, 5, 10, 50, and 100 μg/mL), which was dissolved in DMEM/Ham’s F-12 medium without FBS. The cells were lysed with RIPA Buffer (Thermo Fisher Scientific). Whole cell lysates were subjected to electrophoresis on 10% sodium dodecyl sulfate–polyacrylamide gels (Thermo Fisher Scientific), and then transferred to a polyvinylidene difluoride membrane (Thermo Fisher Scientific). After blocking, the membranes were incubated with the anti-fibroblast growth factor 2 (FGF2) rabbit polyclonal antibody (Santa Cruz Biotechnology, Inc, Santa Cruz, CA, USA) or anti-α-tubulin monoclonal antibody (Santa Cruz Biotech) followed by Novex alkaline-phosphatase conjugated (goat) anti-rabbit or (goat) anti-mouse immunoglobulin G (IgG) secondary antibody (Thermo Fisher Scientific). The antibodies were detected using a chromogenic immunodetection system, WesternBreeze (Thermo Fisher Scientific) according to the manufacturer’s instructions.
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2

Western blot analysis of HCAM and CD13

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Whole cell lysates were prepared using Radioimmunoprecipitation assay (RIPA) buffer (Thermo Fisher scientific) and were subjected to electrophoresis on 10 % SDS-polyacrylamide gels (Thermo Fisher scientific), and then transferred to a PVDF membrane (Thermo Fisher scientific). After blocking, the membranes were incubated with the anti-HCAM (CD44) mouse monoclonal antibody (Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA) and anti-CD13 rabbit monoclonal antibody (Epitomics Inc., Burlingame, CA, USA) followed by Novex® alkaline-phosphatase conjugated (goat) anti-rabbit or (goat) anti-mouse immunoglobulin G (IgG) secondary antibody (Thermo Fisher scientific). The antibodies were detected using a chromogenic immunodetection system, WesternBreeze (Thermo Fisher scientific) according to the manufacturer's instructions. Also, anti- α- tubulin monoclonal antibody (Santa Cruz Biotech.) was used for normalization of Western blot analysis.
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