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WB analysis of HepG2 whole cell lysate using GTX81230 CYP7A1 antibody, C-term. Loading : 20 microg per lane Dilution : 1:1000
WB analysis of HepG2 whole cell lysate using GTX81230 CYP7A1 antibody, C-term. Loading : 20 microg per lane Dilution : 1:1000
WB analysis of HepG2 whole cell lysate using GTX81230 CYP7A1 antibody, C-term. Loading : 20 microg per lane Dilution : 1:1000

CYP7A1 antibody, C-term

GTX81230
GeneTex
ApplicationsWestern Blot
DownloadDatasheet
Product group Antibodies
TargetCYP7A1
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Overview

  • Supplier
    GeneTex
  • Product Name
    CYP7A1 antibody, C-term
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID1581
  • Target name
    CYP7A1
  • Target description
    cytochrome P450 family 7 subfamily A member 1
  • Target synonyms
    24-hydroxycholesterol 7-alpha-hydroxylase; cholesterol 7-alpha-hydroxylase; cholesterol 7alpha-hydroxylase; cholesterol 7-alpha-monooxygenase; CP7A; CYP7; CYPVII; cytochrome P450 7A1; cytochrome P450, family 7, subfamily A, polypeptide 1; cytochrome P450, subfamily VIIA polypeptide 1
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP22680
  • Protein Name
    Cholesterol 7-alpha-monooxygenase
  • 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 membrane protein catalyzes the first reaction in the cholesterol catabolic pathway in the liver, which converts cholesterol to bile acids. This reaction is the rate limiting step and the major site of regulation of bile acid synthesis, which is the primary mechanism for the removal of cholesterol from the body. Polymorphisms in the promoter of this gene are associated with defects in bile acid synthesis. [provided by RefSeq, Feb 2010]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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Figure 1. Western blot analysis of CYP7A1 using anti-CYP7A1 antibody (A01601). 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 HCCT tissue lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human HL-60 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-CYP7A1 antigen affinity purified polyclonal antibody (Catalog # A01601) 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 CYP7A1 at approximately 58 kDa. The expected band size for CYP7A1 is at 58 kDa.
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