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Western Blot analysis of Hela cell using ATG4B Polyclonal Antibody at dilution of 1:500
Western Blot analysis of Hela cell using ATG4B Polyclonal Antibody at dilution of 1:500
Western Blot analysis of Hela cell using ATG4B Polyclonal Antibody at dilution of 1:500

APG4B Polyclonal Antibody

E-AB-15507
Elabscience
Product group Antibodies
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Overview

  • Supplier
    Elabscience
  • Product Name
    APG4B Polyclonal Antibody
  • Delivery Days Customer
    12
  • Applications Supplier
    ELISA WB
  • Certification
    Research Use Only
  • Concentration
    0.3mg/ml
  • Scientific Description
    Autophagy is the process by which endogenous proteins and damaged organelles are destroyed intracellularly. Autophagy is postulated to be essential for cell homeostasis and cell remodeling during differentiation, metamorphosis, non-apoptotic cell death, and aging. Reduced levels of autophagy have been described in some malignant tumors, and a role for autophagy in controlling the unregulated cell growth linked to cancer has been proposed. This gene encodes a member of the autophagin protein family. The encoded protein is also designated as a member of the C-54 family of cysteine proteases. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
  • UNSPSC
    12352203

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Figure 1. Western blot analysis of ATG4B using anti-ATG4B antibody (A02885-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: human RT4 whole cell lysates, Lane 6: human MCF-7 whole cell lysates, Lane 7: human MOLT-4 whole cell lysates, Lane 8: human HEL whole cell lysates, Lane 9: rat brain tissue lysates, Lane 10: rat liver tissue lysates, Lane 11: rat RH35 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATG4B antigen affinity purified polyclonal antibody (Catalog # A02885-1) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATG4B at approximately 48 kDa. The expected band size for ATG4B is at 48 kDa.
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