Recombinant Anti-CFTR Vesicular Antibody, EV Displayed (VS-0425-YC395)

CAT#: VS-0425-YC395

The Recombinant Anti-CFTR Vesicular Antibody, EV Displayed (VS-0425-YC395) 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 CFTR-expressed cells or tissues. The CFTR is a chloride channel protein crucial for ion transport and epithelial function, with mutations causing cystic fibrosis.

Gene Expression
Figure 1 High expression in pancreas Figure 2 Low expression in skeletal muscle. Figure 3 Low expression in lymph node Figure 4 Pancreas Figure 5 RNA cell line category: Group enriched (CACO-2, MOLT-4, U-266/70)

Recombinant Antibody

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

Engineered EVs

  • EV-sorting domain
  • CD63
  • Fc-binding domain
  • z domain
  • EV Size
  • 30~150 nm
  • Producing Cell
  • HEK293F
  • Isolation Method
  • Gradient centrifugation
  • Purification
  • qEV size exclusion chromatography
  • Binding Affinity
  • Kd = 0.85 µg/mL
  • Concentration
  • 1 x 10¹⁰
  • Size
  • 1 mL
  • Buffer
  • PBS
  • Storage
  • Store at -80°C for 12 months

Target

  • Full Name
  • CF transmembrane conductance regulator
  • Biological Process
  • Ion transport, Transport
  • Molecular Function
  • Chloride channel, Ion channel, Isomerase
  • Introduction
  • This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. The encoded protein functions as a chloride channel, making it unique among members of this protein family, and controls ion and water secretion and absorption in epithelial tissues. Channel activation is mediated by cycles of regulatory domain phosphorylation, ATP-binding by the nucleotide-binding domains, and ATP hydrolysis. Mutations in this gene cause cystic fibrosis, the most common lethal genetic disorder in populations of Northern European descent. The most frequently occurring mutation in cystic fibrosis, DeltaF508, results in impaired folding and trafficking of the encoded protein. Multiple pseudogenes have been identified in the human genome.
  • Alternative Names
  • ABC35, ABCC7, CF, CFTR/MRP, dJ760C5.1, MRP7, TNR-CFTR
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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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