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Western blot analysis of extracts of Mouse testis using CYP51A1 Polyclonal Antibody at dilution of 1:1000.
Western blot analysis of extracts of Mouse testis using CYP51A1 Polyclonal Antibody at dilution of 1:1000.
Western blot analysis of extracts of Mouse testis using CYP51A1 Polyclonal Antibody at dilution of 1:1000.

CYP51A1 Polyclonal Antibody

E-AB-64668
Elabscience
Product group Antibodies
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Overview

  • Supplier
    Elabscience
  • Product Name
    CYP51A1 Polyclonal Antibody
  • Delivery Days Customer
    12
  • Certification
    Research Use Only
  • Scientific Description
    This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum protein participates in the synthesis of cholesterol by catalyzing the removal of the 14alpha-methyl group from lanosterol. Homologous genes are found in all three eukaryotic phyla, fungi, plants, and animals, suggesting that this is one of the oldest cytochrome P450 genes. Two transcript variants encoding different isoforms have been found for this gene.
  • UNSPSC
    12352203

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Figure 1. Western blot analysis of CYP51A1/CYP51 using anti-CYP51A1/CYP51 antibody (A04032-1). 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 30ug of sample under reducing conditions. Lane 1: monkey COS-7 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: mouse liver tissue lysates, Lane 5: mouse kidney tissue lysates. After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA 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-CYP51A1/CYP51 antigen affinity purified polyclonal antibody (Catalog # A04032-1) 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 CYP51A1/CYP51 at approximately 57KD. The expected band size for CYP51A1/CYP51 is at 57KD.
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