Recombinant Anti-SCARB2 Vesicular Antibody, EV Displayed (VS-0425-YC398)

CAT#: VS-0425-YC398

The Recombinant Anti-SCARB2 Vesicular Antibody, EV Displayed (VS-0425-YC398) 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 SCARB2-expressed cells or tissues. The SCARB2 is a glycoprotein located in lysosomal membranes, linked to membrane transport processes and associated with myoclonic epilepsy.

Gene Expression
Figure 1 IF staining of human cell line A-431 Figure 2 IHC staining of human prostate Figure 3 IHC staining of human pancreas Figure 4 Cerebral cortex Figure 5 Colon Figure 6 Liver Figure 7 Kidney Figure 8 Testis Figure 9 RNA cell line category: Cell line enhanced (ASC diff)

Recombinant Antibody

  • Application
  • Block, ELISA, FC, Cell-uptake
  • Product Type
  • Ab-Fc-EVs
  • Antibody Quantification (Ab/EV)
  • ~100 Ab/EV
  • Target
  • SCARB2
  • 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
  • Scavenger receptor class B member 2
  • Biological Process
  • Host-virus interaction
  • Molecular Function
  • Host cell receptor for virus entry, Receptor
  • Cellular Localization
  • Cytosol
  • Introduction
  • The protein encoded by this gene is a type III glycoprotein that is located primarily in limiting membranes of lysosomes and endosomes. Earlier studies in mice and rat suggested that this protein may participate in membrane transportation and the reorganization of endosomal/lysosomal compartment. The protein deficiency in mice was reported to impair cell membrane transport processes and cause pelvic junction obstruction, deafness, and peripheral neuropathy. Further studies in human showed that this protein is a ubiquitously expressed protein and that it is involved in the pathogenesis of HFMD (hand, foot, and mouth disease) caused by enterovirus-71 and possibly by coxsackievirus A16. Mutations in this gene caused an autosomal recessive progressive myoclonic epilepsy-4 (EPM4), also known as action myoclonus-renal failure syndrome (AMRF). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
  • Alternative Names
  • CD36L2, HLGP85, LIMP-2, LIMPII, SR-BII
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For research use only. Not intended for any clinical use. No products from Creative Biolabs may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative Biolabs.

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