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Mouse anti rpa34 20

Manufactured by Merck Group

Mouse anti-RPA34–20 is a monoclonal antibody that specifically recognizes the RPA34–20 subunit of the Replication Protein A (RPA) complex. RPA is a heterotrimeric protein complex that plays a crucial role in DNA replication, repair, and recombination. The Mouse anti-RPA34–20 antibody can be used for the detection and analysis of the RPA34–20 subunit in various experimental applications.

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3 protocols using mouse anti rpa34 20

1

Immunoprecipitation Profiling of DNA Repair Proteins

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Immunoprecipitation experiments were performed using 3×106 293T cells. IP buffer (0.5% Triton X-100, 50mM Tris HCl pH 8.0, 150 mM NaCl, EGTA 1 mM) supplemented with phosphatase, protease inhibitors and benzonase was used for cells lysis. Two mL of lysate were incubated overnight at 4°C with 20 μl of Anti-Flag M2 magnetic beads (Sigma) or Anti-RPA32 conjugated Dynabeads (2μg of MABE285 anti-RPA34–20 mouse (Millipore) with 40μl of Dynabeads protein G (Invitrogen). After extensive washing in IP buffer, proteins were released in 2X Laemmli buffer buffer and subjected to Western blotting.
Blots were incubated with primary antibodies: rabbit anti-FLAG (Sigma-Aldrich); rabbit anti-RPA70 (Genetex); mouse anti-RPA34–20 (Millipore); rabbit anti-pS440/467WRN (Abgent; custom-made); rabbit anti-Lamin B1 (Abcam); rabbit anti-RAD51 (Santa Cruz); rabbit anti-GST (Calbiochem). Blots were detected using the Western blotting detection kit WesternBright ECL (Advansta) according to the manufacturer’s instructions. Quantification was performed on scanned images of blots using Image Lab software, and values shown on the graphs represent normalization of the protein content evaluated through Lamin B1 or Immunoprecipitated protein immunoblotting.
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2

WRN Phosphorylation Regulates RPA32 Binding

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GST and GST-WRN fragments (phosphorylated or not) were incubated with 300ng of 293T cell extracts. After 16hrs of incubation, fragments were separated from the beads and RPA32 interaction with WRN fragments were measured with densitometric analysis by WB using rabbit anti-GST (Calbiochem), rabbit anti-p440WRN (Abgent) and mouse anti-RPA34–20 (Millipore).
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3

In Situ Protein Interaction Assay

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Cells were cultured onto 8-well Nunc chamber-slides. The in situ proximity ligation assay (PLA) in combination with immunofluorescence microscopy was performed using the Duolink Detection (Merck) or the NaveniFlex (Navinci diagnostics) Kit with anti-Mouse PLUS and anti-Rabbit MINUS PLA Probes, according to the manufacturer’s instructions. To detect proteins, we used rabbit anti-WRN (Abcam), rabbit anti-Flag (Sigma-Aldrich), mouse anti-RPA34–20 (Millipore), rabbit anti-RAD51 (Santa Cruz) and mouse anti-IdU antibody (Becton Dickinson) antibodies.
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