Recombinant Anti-AMHR2 Vesicular Antibody, EV Displayed (VS-0425-YC299)

CAT#: VS-0425-YC299

The Recombinant Anti-AMHR2 Vesicular Antibody, EV Displayed (VS-0425-YC299) 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 AMHR2-expressed cells or tissues. The AMHR2 is a receptor for anti-Mullerian hormone, affecting male differentiation by preventing the development of Mullerian ducts. Mutations cause persistent Mullerian duct syndrome.

Gene Expression
Figure 1 IF staining of human cell line HEL Figure 2 IF staining of human cell line HEK 293 Figure 3 IF staining of human cell line CACO-2 Figure 4 IF staining of human cell line A-434 Figure 5 RNA cell line category: Group enriched (HEL, K-562)

Recombinant Antibody

  • Application
  • ELISA, FC, Cell-uptake
  • Product Type
  • Ab-Fc-EVs
  • Antibody Quantification (Ab/EV)
  • ~100 Ab/EV
  • Target
  • AMHR2
  • Host Animal
  • Mouse
  • Antibody Isotype
  • IgG1 kappa
  • Species Reactivity
  • Human
  • Expression Cell
  • Mammalian cell

Engineered EVs

  • EV-sorting domain
  • CD63
  • Fc-binding domain
  • Protein G
  • 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
  • Anti-Mullerian hormone receptor type 2
  • Molecular Function
  • Kinase, Receptor, Serine/threonine-protein kinase, Transferase
  • Cellular Localization
  • Vesicles, Nucleoplasm, Cytosol
  • Introduction
  • This gene encodes the receptor for the anti-Mullerian hormone (AMH) which, in addition to testosterone, results in male sex differentiation. AMH and testosterone are produced in the testes by different cells and have different effects. Testosterone promotes the development of male genitalia while the binding of AMH to the encoded receptor prevents the development of the mullerian ducts into uterus and Fallopian tubes. Mutations in this gene are associated with persistent Mullerian duct syndrome type II. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Sep 2009]
  • Alternative Names
  • MISR2, MISRII
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