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Anti pkm2 monoclonal antibody

Manufactured by Cell Signaling Technology
Sourced in United States, United Kingdom

The Anti-PKM2 monoclonal antibody is a laboratory research tool designed to detect and study the pyruvate kinase M2 (PKM2) protein, which plays a crucial role in cellular metabolism. This antibody can be used in various immunoassay techniques, such as Western blotting, immunohistochemistry, and immunoprecipitation, to facilitate the investigation of PKM2 expression and function in biological samples.

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2 protocols using anti pkm2 monoclonal antibody

1

Amoebic Colitis Pathogenesis in Mice

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Eight-week-old male C3H/HeNCrl mice were obtained from Beijing Vital River Laboratory Animal Technology Company. Amoebic colitis was induced by directly inoculating 1 × 106 axenic E. histolytica SAW755CR trophozoites into the cecum (n = 6), and the control group received the same volume of medium without trophozoites (n = 4). Six days after inoculation, the cecum tissues were harvested and fixed in 4% paraformaldehyde, followed by paraffin embedding. Tissue sections were stained with hematoxylin and eosin or periodic acid-Schiff (PAS) stain for histopathological analysis. Furthermore, immunohistochemical staining was performed using anti-PKM2 monoclonal antibody (Cell Signaling Technology, D78A4; Boston, MA, USA) to detect the expression level of PKM2 in the cecum.
All animal experiments were performed in strict accordance with the guidelines of the Regulations for the Administration of Affairs Concerning Experimental Animals (1988.11.1) and approved by the Institutional Animal Care and Use Committee (permit no. 20160225-097). All efforts were made to minimize animal suffering.
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2

Western Blotting to Validate Proteomics Findings

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Western blotting was performed to confirm the results of quantitative proteomics. Briefly, protein samples of CHO cells and Caco2 cells stimulated with E. histolytica or Igl were separated on 10% polyacrylamide gels and then electrotransferred to polyvinylidene difluoride membranes (General Electric Co., Schenectady, NY, USA). After blocking with bovine serum albumin (5% in PBS), membranes were incubated with the following primary antibodies: anti-β-actin antibody (Abcam, Ab8227; Cambridge, United Kingdom), anti-PKM2 monoclonal antibody (Cell Signaling Technology, catalog no. 4053; Boston, MA, USA), and anti-LC3A/B antibody (Cell Signaling Technology, catalog no. 12741; Boston, MA, USA). Horseradish peroxidase (HRP)-conjugated goat anti-rabbit IgG(H+L) (Abcam, Ab6721; Cambridge, United Kingdom) was used as the secondary antibody. Proteins were detected using an enhanced chemiluminescence (ECL) Western blotting substrate kit (Tanon, Shanghai, China).
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