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Western Blot analysis of A549, 231, PC3 and hela cell using MAD2L1BP Polyclonal Antibody at dilution of 1:675
Western Blot analysis of A549, 231, PC3 and hela cell using MAD2L1BP Polyclonal Antibody at dilution of 1:675
Western Blot analysis of A549, 231, PC3 and hela cell using MAD2L1BP Polyclonal Antibody at dilution of 1:675

MAD2L1BP Polyclonal Antibody

E-AB-14202
Elabscience
Product group Antibodies
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Overview

  • Supplier
    Elabscience
  • Product Name
    MAD2L1BP Polyclonal Antibody
  • Delivery Days Customer
    12
  • Applications Supplier
    ELISA WB IHC
  • Certification
    Research Use Only
  • Concentration
    0.9mg/ml
  • Scientific Description
    The protein encoded by this gene was identified as a binding protein of the MAD2 mitotic arrest deficient-like 1 (MAD2/MAD2L1). MAD2 is a key component of the spindle checkpoint that delays the onset of anaphase until all the kinetochores are attached to the spindle. This protein may interact with the spindle checkpoint and coordinate cell cycle events in late mitosis. Alternatively spliced transcript variants encoding distinct isoforms have been observed.
  • UNSPSC
    12352203

FAQ

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Figure 1. Western blot analysis of MAD2L1BP using anti-MAD2L1BP antibody (A06825-2). 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 A431 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human THP-1 whole cell lysates, Lane 5: human HepG2 whole cell lysates, Lane 6: human HEL whole cell lysates, Lane 7: human 293T whole cell lysates, Lane 8: human SH-SY5Y 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-MAD2L1BP antigen affinity purified polyclonal antibody (Catalog # A06825-2) 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 MAD2L1BP at approximately 37 kDa. The expected band size for MAD2L1BP is at 37 kDa.
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