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Anti sqstm1 p62 antibody

Manufactured by Cell Signaling Technology
Sourced in United States

The Anti-SQSTM1/p62 antibody is a laboratory reagent used to detect the SQSTM1/p62 protein. SQSTM1/p62 is a multifunctional protein involved in various cellular processes. This antibody can be used to study the expression and localization of SQSTM1/p62 in biological samples.

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4 protocols using anti sqstm1 p62 antibody

1

Protein Expression and Antibody Validation

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Anti-TRIM44 polyclonal antibody (Proteintech Group, 11,511-1-AP); anti-Ub antibody (Biolegend, 646,301); anti-mCherry antibody (ThermoFisher, PA5-34,974); anti-VIM antibody (ThermoFisher, MA5-11,883); anti-NFE2L2/NRF2 antibody (ThermoFisher, PA5-27,882); anti-20S proteasome antibody (MilliporeSigma, ST1049); anti-TUBG/γ-Tubulin antibody (MilliporeSigma, T5326); anti-ATG5 antibody (Novus Biologicals, NBP2-24,389); Anti-GFP antibody (Santa Cruz Biotechnology, sc-9996); anti-ACTB/β-Actin antibody (Santa Cruz Biotechnology, sc-47,778), anti-HA antibody (Santa Cruz Biotechnology, sc-805); anti-BECN1 antibody (Cell Signaling Technology, 4122); anti-HDAC6 antibody (Cell Signaling Technology, 7558); anti-LC3B antibody (Cell Signaling Technology, 3868); anti-SQSTM1/p62 antibody (Cell Signaling Technology, 88,588); anti-cleaved PARP antibody (Cell Signaling Technology, 5625); Alexa Fluor 594 donkey anti rabbit IgG(H + L) (Invitrogen, A21207); Alexa Fluor 546 goat anti mouse IgG(H + L) (Invitrogen, A11003).
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2

α-Synuclein Detection and Quantification

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Proteins were separated on precast polyacrylamide gels (Bio-Rad) and transferred to Hybond (Amersham). For detection of α-synuclein, proteins were cross-linked to membranes using 0.4% paraformaldehyde (51 , 52 ). Chemiluminescent detection was performed with enhanced chemiluminescence (Amersham). Antibodies used were anti-α-synuclein antibody ([1:1500], BD Transduction Laboratories, 610787), anti-Ataxin-2 antibody ([1:4000], BD Biosciences, 611378), anti-Staufen antibody ([1:5000], Novus Biologicals, NBP1-33202), anti-BiP antibody ([1:3000], Genetex, GTX113340), anti-CHOP antibody ([1:3000], Cell Signaling Technology, 2895), anti-mTOR antibody ([1:4000], Cell Signaling Technology, 2972), anti-SQSTM1/p62 antibody ([1:4000], Cell Signaling Technology, 5114), anti-LC3B antibody ([1:7000], Novus Biologicals, NB100-2220SS), anti-tyrosine hydroxylase antibody ([1:2000], Millipore-Sigma, AB152), and peroxidase-conjugated monoclonal anti-β-Actin antibody (clone AC-15) ([1:20,000], Sigma-Aldrich, A3854). The secondary antibody was peroxidase-conjugated anti-rabbit (Jackson ImmunoResearch Laboratories).
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3

Immunohistochemical Analysis of p62 in Mouse Liver

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Liver sections of 4 μm thickness were cut from PFA-fixed paraffin-embedded blocks of mouse liver. The sections were stained with anti-SQSTM1/p62 antibody (#23214, Cell Signaling Technology) according to the manufacturer’s protocol.
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4

Plasmid Construction for Autophagy Study

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The pcDNA EGFP-RFP-LC3B plasmid encoding EGFP, RFP, and LC3B was constructed by the pcDNA 3.1 myc-his (-) vector. The pcDNA EGFP-mRFP-LC3B (ptfLC3) plasmid encoding Chlorocebus sabaeus LC3B (NCBI Reference Sequence: XM_007994295.2) was constructed by the pcDNA 3.1 myc-his (-) vector. Anti-LC3B antibody (Cell Signaling, Danvers, MA, USA, #2775), anti-SQSTM1/p62 antibody (Cell Signaling, #5114), anti-ATG5 antibody (Cell Signaling, #9980), anti-ATG12 antibody (Cell signaling, #4180), anti-LAMP1 (Cell Signaling, #3243), anti-β-actin (Santa Cruz, sc-47778), and mouse anti-PEDV antibody were made in our laboratory (immunized inactivated PEDV in mouse).
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