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FACS analysis of PFA-fixed A431 cells using GTX01092 MEFV antibody. Blue : Primary antibody Black : IgG control Permeabilization : 0.15% Triton X-100 Dilution : 10microg/ml
FACS analysis of PFA-fixed A431 cells using GTX01092 MEFV antibody. Blue : Primary antibody Black : IgG control Permeabilization : 0.15% Triton X-100 Dilution : 10microg/ml
FACS analysis of PFA-fixed A431 cells using GTX01092 MEFV antibody. Blue : Primary antibody Black : IgG control Permeabilization : 0.15% Triton X-100 Dilution : 10microg/ml

MEFV antibody

GTX01092
GeneTex
ApplicationsFlow Cytometry, ImmunoFluorescence, ImmunoCytoChemistry
DownloadDatasheet
Product group Antibodies
TargetMEFV
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Overview

  • Supplier
    GeneTex
  • Product Name
    MEFV antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    ICC/IF: 10microg/ml. FACS: 10microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Flow Cytometry, ImmunoFluorescence, ImmunoCytoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.5 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID4210
  • Target name
    MEFV
  • Target description
    MEFV innate immuity regulator, pyrin
  • Target synonyms
    FMF; marenostrin; Mediterranean fever; MEF; MEFV, pyrin innate immunity regulator; PAAND; pyrin; TRIM20
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDO15553
  • Protein Name
    Pyrin
  • Scientific Description
    This gene encodes a protein, also known as pyrin or marenostrin, that is an important modulator of innate immunity. Mutations in this gene are associated with Mediterranean fever, a hereditary periodic fever syndrome. [provided by RefSeq, Jul 2008]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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Figure 1. Western blot analysis of Pyrin/MEFV using anti-Pyrin/MEFV antibody (A00764-1). 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 U-87MG whole cell lysates, Lane 3: human Raji whole cell lysates, Lane 4: mouse spleen tissue lysates, Lane 5: mouse lung tissue 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-Pyrin/MEFV antigen affinity purified polyclonal antibody (Catalog # A00764-1) 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 Pyrin/MEFV at approximately 86 kDa. The expected band size for Pyrin/MEFV is at 86 kDa.
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