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IHC-P analysis of human lung carcinoma tissue using GTX51679 CD200 antibody. Antigen retrieval : Boiling in sodium citrate buffer (pH6) for 15min Dilution : 1:400
IHC-P analysis of human lung carcinoma tissue using GTX51679 CD200 antibody. Antigen retrieval : Boiling in sodium citrate buffer (pH6) for 15min Dilution : 1:400
IHC-P analysis of human lung carcinoma tissue using GTX51679 CD200 antibody. Antigen retrieval : Boiling in sodium citrate buffer (pH6) for 15min Dilution : 1:400

CD200 antibody

GTX51679
GeneTex
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetCD200
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Overview

  • Supplier
    GeneTex
  • Product Name
    CD200 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    IHC-P: 1:50-400. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID4345
  • Target name
    CD200
  • Target description
    CD200 molecule
  • Target synonyms
    antigen identified by monoclonal antibody MRC OX-2; CD200 antigen; MOX1; MOX2; MRC; OX-2; OX-2 membrane glycoprotein
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP41217
  • Protein Name
    OX-2 membrane glycoprotein
  • Scientific Description
    The protein encoded by this gene is a type-1 membrane glycoprotein, which contains two immunoglobulin domains, and thus belongs to the immunoglobulin superfamily. Studies of the related genes in mouse and rat suggest that this gene may regulate myeloid cell activity and delivers an inhibitory signal for the macrophage lineage in diverse tissues. Multiple alternatively spliced transcript variants that encode different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Stem cell therapy as a novel therapeutic intervention for resistant cases of alopecia areata and androgenetic alopecia. Elmaadawi IH et al., 2018 Aug, J Dermatolog Treat
    Read more

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Figure 1. Western blot analysis of CD200/OX2 using anti-CD200/OX2 antibody (A01512-1). 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 50ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse brain tissue lysates, Lane 4: mouse SP20 whole cell 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-CD200/OX2 antigen affinity purified polyclonal antibody (Catalog # A01512-1) 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 1:10000 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 CD200/OX2 at approximately 45KD. The expected band size for CD200/OX2 is at 31KD.
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