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D4a7 clone

Manufactured by Cell Signaling Technology

D4A7 clone is a monoclonal antibody that recognizes the SQSTM1/p62 protein. This protein is involved in various cellular processes, including autophagy and signal transduction. The D4A7 clone can be used to detect and study the expression and localization of SQSTM1/p62 in biological samples.

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3 protocols using d4a7 clone

1

Diglycopeptide Enrichment and Profiling

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diGLY capture was performed largely as described (Rose et al., 2016 (link)). The diGly monoclonal antibody (Cell Signaling Technology; D4A7 clone) (32 μg antibody/1 mg peptide) was coupled to Protein A Plus Ultralink resin (1:1 μl slurry/ μg antibody) (Thermo Fisher Scientific) overnight at 4°C prior to its chemical cross-linking reaction. Dried peptides (indicated amount in corresponding figures) were resuspended in 1.5 ml of ice-cold IAP buffer [50 mM MOPS (pH 7.2), 10 mM sodium phosphate and 50 mM NaCl] and centrifuged at maximum speed for 5 min at 4°C to remove any insoluble material. Supernatants (pH ~7.2) were incubated with the antibody beads for 2 hr at 4°C with gentle end-over-end rotation. After centrifugation at 215×g for 2 min, beads were washed three more times with ice-cold IAP buffer and twice with ice-cold PBS. The diGLY peptides were eluted twice with 0.15% TFA, desalted using homemade StageTips and dried via vacuum centrifugation, prior to TMT labeling.
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2

diGLY Immunoprecipitation for TMT Proteomics

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diGLY capture was performed largely as described (25 (link)). The diGLY monoclonal antibody (Cell Signaling Technology; D4A7 clone) (32 μg of antibody/1 mg of peptide) was coupled to Protein A Plus Ultralink resin (1:1 μl of slurry/μg of antibody) (Thermo Fisher Scientific) overnight at 4°C before its chemical cross-linking reaction. Dried peptides (1-mg starting material) were resuspended in 1.5 ml of ice-cold immuno affinity purification (IAP) buffer [50 mM Mops (pH 7.2), 10 mM sodium phosphate, and 50 mM NaCl] and centrifuged at maximum speed for 5 min at 4°C to remove any insoluble material. Supernatants (pH ∼ 7.2) were incubated with the antibody beads for 2 hours at 4°C with gentle end-over-end rotation. After centrifugation at 215g for 2 min, beads were washed three more times with ice-cold IAP buffer and twice with ice-cold PBS. The diGLY peptides were eluted twice with 0.15% trifluoroacetic acid, desalted using homemade StageTips, and dried via vacuum centrifugation, before TMT labeling. A detailed protocol describing the diGLY immunoprecipitation for TMT proteomics has been reported (dx.doi.org/10.17504/protocols.io.buyunxww).
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3

Immunoaffinity Enrichment of diGLY Peptides

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diGLY capture was performed largely as described (Rose et al., 2016 (link)) . The diGly monoclonal antibody (Cell Signaling Technology; D4A7 clone) (32 μg antibody/1 mg peptide) was coupled to Protein A Plus Ultralink resin (1:1 μL slurry/ μg antibody) (Thermo Fisher Scientific) overnight at 4°C prior to its chemical cross-linking reaction. Dried peptides (indicated amount in corresponding figures) were resuspended in 1.5 mL of ice-cold IAP buffer [50 mM MOPS (pH 7.2), 10 mM sodium phosphate and 50 mM NaCl] and centrifuged at maximum speed for 5 min at 4°C to remove any insoluble material. Supernatants (pH ∼7.2) were incubated with the antibody beads for 2 hr at 4°C with gentle end-over-end rotation. After centrifugation at 215 × g for 2 min, beads were washed three more times with ice-cold IAP buffer and twice with ice-cold PBS. The diGLY peptides were eluted twice with 0.15% TFA, desalted using homemade StageTips and dried via vacuum centrifugation, prior to TMT labeling.
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