Recombinant Anti-PRNP Vesicular Antibody, EV Displayed (VS-0425-YC520)

CAT#: VS-0425-YC520

The Recombinant Anti-PRNP Vesicular Antibody, EV Displayed (VS-0425-YC520) is an antibody-displaying extracellular vesicle (Ab-EV). The product combines the benefits of both extracellular vesicle (EV) and antibody (Ab) which can guide the decorated EVs to PRNP-expressed cells or tissues. PRNP is a glycosylphosphatidylinositol-anchored glycoprotein with regions prone to aggregation. Mutations in PRNP are linked to diseases like Creutzfeldt-Jakob and fatal familial insomnia. An overlapping open reading frame produces a smaller protein, AltPrP.

Gene Expression
Figure 1 IF staining of human cell line U-2 OS Figure 2 IHC staining of human cerebellum Figure 3 Cerebral cortex Figure 4 Caudate Figure 5 Colon Figure 6 RNA cell line category: Cell line enhanced (WM-115)

Recombinant Antibody

  • Application
  • ELISA, FC, Inhib, Cell-uptake
  • Product Type
  • Ab-Fc-EVs
  • Antibody Quantification (Ab/EV)
  • ~100 Ab/EV
  • Target
  • PRNP
  • Host Animal
  • Mouse
  • Antibody Isotype
  • IgG
  • Species Reactivity
  • Human
  • Expression Cell
  • Mammalian cell

Engineered EVs

  • EV-sorting domain
  • CD63
  • Fc-binding domain
  • Protein A
  • EV Size
  • 30~150 nm
  • Producing Cell
  • HEK293F
  • Isolation Method
  • Gradient centrifugation
  • Purification
  • qEV size exclusion chromatography
  • Concentration
  • 1 x 10¹⁰
  • Size
  • 1 mL
  • Buffer
  • PBS
  • Storage
  • Store at -80°C for 12 months

Target

  • Full Name
  • Prion protein
  • Biological Process
  • Cell cycle, Growth arrest
  • Molecular Function
  • Prion
  • Cellular Localization
  • Nuclear membrane, Cytosol, Vesicles
  • Introduction
  • The protein encoded by this gene is a membrane glycosylphosphatidylinositol-anchored glycoprotein that tends to aggregate into rod-like structures. The encoded protein contains a highly unstable region of five tandem octapeptide repeats. This gene is found on chromosome 20, approximately 20 kbp upstream of a gene which encodes a biochemically and structurally similar protein to the one encoded by this gene. Mutations in the repeat region as well as elsewhere in this gene have been associated with Creutzfeldt-Jakob disease, fatal familial insomnia, Gerstmann-Straussler disease, Huntington disease-like 1, and kuru. An overlapping open reading frame has been found for this gene that encodes a smaller, structurally unrelated protein, AltPrp.
  • Alternative Names
  • AltPrP, CD230, CJD, GSS, PRIP, PRP
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