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Mouse anti pgk1 22c5

Manufactured by Abcam
Sourced in United Kingdom, Switzerland

Mouse anti-Pgk1 22C5 is a primary antibody that recognizes the phosphoglycerate kinase 1 (Pgk1) protein. Pgk1 is a key enzyme in the glycolytic pathway, catalyzing the conversion of 1,3-bisphosphoglycerate to 3-phosphoglycerate. The 22C5 clone of this antibody can be used to detect and study the Pgk1 protein in various applications.

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3 protocols using mouse anti pgk1 22c5

1

Cell Lysis and Western Blotting Protocol

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Cell lysis and western blotting was done as described (Szoradi et al., 2018 (link)). In brief, cells were disrupted by bead beating, proteins were solubilized with SDS, protein determination was carried out with the BCA assay kit (Thermo Fisher Scientific Pierce, Waltham, Massachusetts), equal amounts of protein were resolved by SDS-PAGE and transferred onto nitrocellulose membranes. Membranes were probed with primary and HRP-coupled secondary antibodies, developed with homemade ECL, and chemiluminescence was detected with an ImageQuant LAS 4000 imaging system (GE Healthcare, Chalfont St Giles, UK). Images were quantified with ImageJ and processed with Adobe Photoshop. Primary antibodies were rat anti-HA 3F10 (Roche, Basel, Switzerland), rabbit anti-Kar2 (Peter Walter, UCSF), rabbit anti-mCherry (Biovision, Milpitas, California) and mouse anti-Pgk1 22C5 (Abcam, Cambridge, UK).
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2

Cell Lysis and Western Blotting

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Cell lysis and Western blotting were done as described (Szoradi et al, 2018). Primary antibodies were mouse anti‐Pho8 1D3A10 (Abcam, Cambridge, UK), mouse anti‐GFP 7.1/13.1 (Roche, Basel, Switzerland), and mouse anti‐Pgk1 22C5 (Abcam).
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3

Protein Extraction and Western Blotting

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Cells were collected by centrifugation, washed once with water and disrupted by bead beating with a FastPrep 24 (MP Biomedicals) in 50 mM Tris-HCl pH 7.5 containing 0.5 mM EDTA, 1 mM PMSF and complete protease inhibitors (Roche). Proteins were solubilized by addition of 1.5% SDS and incubation at 65 C for 5 min. Lysates were cleared at 16,000 g at 4 C for 2 min and protein concentrations were determined with the BCA assay kit (Thermo Scientific Pierce). Equal amounts of protein were resolved by SDS-PAGE and transferred onto nitrocellulose membranes. Membranes were probed with primary and HRP-coupled secondary antibodies and incubated with homemade ECL. Chemiluminescence was detected with an ImageQuant LAS 4000 imaging system (GE Healthcare). Images were quantified with ImageJ and processed with Adobe Photoshop. Antibodies were mouse-anti GFP 7.1/13.1 (Roche), mouse anti-mCherry 1C51 (Abcam) for detection of Luciferase-mCherry, rabbit anti-mCherry (Biovision) for detection of R-mCherry-sfGFP, rabbit anti-Sec61 (Peter Walter, UCSF), mouse anti-Pgk1 22C5 (Abcam), mouse anti-Pho8 1D3A10 (Abcam), mouse anti-FLAG M2 (Sigma), mouse anti-HA 6E2 (Cell Signaling) for detection of CFTR-HA, and rat anti-HA 3F10 (Roche) for detection of HA-tagged Roq1.
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