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Western Blot analysis of A172 and PC3 cell using ACLY Polyclonal Antibody at dilution of 1:1050
Western Blot analysis of A172 and PC3 cell using ACLY Polyclonal Antibody at dilution of 1:1050
Western Blot analysis of A172 and PC3 cell using ACLY Polyclonal Antibody at dilution of 1:1050

ACLY Polyclonal Antibody

E-AB-14775
Elabscience
Product group Antibodies
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Overview

  • Supplier
    Elabscience
  • Product Name
    ACLY Polyclonal Antibody
  • Delivery Days Customer
    12
  • Applications Supplier
    ELISA WB
  • Certification
    Research Use Only
  • Concentration
    0.6mg/ml
  • Scientific Description
    ATP citrate lyase is the primary enzyme responsible for the synthesis of cytosolic acetyl-CoA in many tissues. The enzyme is a tetramer (relative molecular weight approximately 440,000) of apparently identical subunits. It catalyzes the formation of acetyl-CoA and oxaloacetate from citrate and CoA with a concomitant hydrolysis of ATP to ADP and phosphate. The product, acetyl-CoA, serves several important biosynthetic pathways, including lipogenesis and cholesterogenesis. In nervous tissue, ATP citrate-lyase may be involved in the biosynthesis of acetylcholine. Two transcript variants encoding distinct isoforms have been identified for this gene.
  • UNSPSC
    12352203

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Figure 1. Western blot analysis of ACLY using anti-ACLY antibody (PB10024). 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 A549 whole cell lysates, Lane 2: human MOLT4 whole cell lysates, Lane 3: human U87 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: human 293T whole cell lysates, Lane 6: human Hela whole cell lysates, Lane 7: human T47D whole cell lysates, Lane 8: human HepG2 whole cell lysates, Lane 9: rat pancreas tissue lysates, Lane 10: mouse NIH/3T3 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-ACLY antigen affinity purified polyclonal antibody (Catalog # PB10024) 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 ACLY at approximately 125 kDa. The expected band size for ACLY is at 125 kDa.
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