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Anti-HPV16 E7 protein [69E2], Human IgG1, kappa

AB03909-10.0
Absolute Antibody
ApplicationsImmunoFluorescence, Western Blot, CLIA ChemiLuminecent ImmunoAssay, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry
Product group Antibodies
TargetE7
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Overview

  • Supplier
    Absolute Antibody
  • Product Name
    Anti-HPV16 E7 protein [69E2], Human IgG1, kappa
  • Delivery Days Customer
    9
  • Application Supplier Note
    The binding characterization of this antibody for HPV E7 protein was done using ELISA. The original IgG2a version of this antibody binds HPV E7 protein with a binding affinity of Kd= 5.6 nM. The anti-HPVE7 protein antibody 79A11 can be used as capture antibody in combination with HRP conjugated 69E2 antibody as a detection antibody in a sandwich ELISA. This antibody can be used for the detection of HPV E7 protein from cells lysates of cervical cancer cell lines CaSki cells and HeLa cells in a western blot. This antibody was also used in the immunocytochemical analysis of CaSki cells and HeLa cells (HPV positive). This antibody was used for the immunohistochemical analysis of HPV16-positive cervical cancer squamous cell carcinoma and HPV18-positive cervical cancer adenocarcinoma. This antibody was also used for the indirect immunofluorescence staining of CaSki cells and HeLa cells. A chemiluminescent immunoassay was prepared using 79A11 as capture and Biotin-69E2 and HRP-Streptavidin for detection (CN111410689).
  • Applications
    ImmunoFluorescence, Western Blot, CLIA ChemiLuminecent ImmunoAssay, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    69E2
  • Gene ID1489079
  • Target name
    E7
  • Target description
    transforming protein E7
  • Target synonyms
    HpV16gp2; transforming protein E7
  • Host
    Human
  • Isotype
    IgG1
  • Protein IDP03129
  • Protein Name
    Protein E7
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352203

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Hela (Positive) and RSC96 (Negative control) cells (black) were incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with Integrin alpha HPV16-E7Antibody (bs-10446R) at 1:50 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2% BSA in PBS, followed by secondary antibody(blue) incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange)._x000D_
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References
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