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Ab391

Manufactured by Abcam

Ab391 is a primary antibody that targets the human GAPDH protein. It is a rabbit polyclonal antibody produced using a synthetic peptide conjugated to KLH as the immunogen. The antibody is provided in liquid form and can be used for applications such as Western blotting, immunohistochemistry, and immunocytochemistry.

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2 protocols using ab391

1

Characterizing Lysozyme-LPS Interactions

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Gel filtration chromatography was carried out using an Enrich SEC 650 (10/300) column (Bio Rad) [18 (link),22 (link)]. For analysis, 500 μL of lysozyme (500 μg/mL) and 500 μL of LPS (500 μg/mL) were mixed and then incubated for 30 min at 37 °C at room temperature, and applied to the column at a flow rate of 1.0 mL/min. The elution profile was analyzed by monitoring A215, and by SDS-PAGE and western blot analyses of the fractions using an affinity-purified anti-lysozyme antibody (1:500 dilution, ab391, Abcam).
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2

Western Blot Analysis of RBC Ghosts

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RBCs isolated from each recipient group 2 days after immunization with anti-HEL monoclonal antibodies were lysed in 5 mmol/L sodium phosphate (pH 7.5) with protease inhibitor cocktail (Sigma Roche) at 4°C and centrifuged at 14,000 rpm, as outlined previously.29 (link),48 (link) RBC ghosts were then subjected to western blot analysis with rabbit polyclonal anti-HEL (Abcam, ab391, 1:5,000) and detection with goat anti-rabbit horseradish peroxidase (Abcam, ab205718 1:10,000). Mouse monoclonal anti–glyceraldehyde 3-phosphate dehydrogenase (clone: GA1R, 1:1,000), followed by goat anti-mouse IgG1 horseradish peroxidase (Bethyl Laboratories, 1:10,000) was applied following stripping membranes with 25 mM glycine hydrochloride with 1% sodium dodecyl sulfate, pH 2. All membranes were developed using a chemiluminescence reagent (HyGlo ECL, Denville Scientific Inc.).
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