Recombinant Anti-GJA1 Vesicular Antibody, EV Displayed (VS-0425-YC474)

CAT#: VS-0425-YC474

The Recombinant Anti-GJA1 Vesicular Antibody, EV Displayed (VS-0425-YC474) 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 GJA1-expressed cells or tissues. The GJA1 is a gap junction protein critical for heart function and development, with mutations linked to several disorders.

Gene Expression
Figure 1 IF staining of human cell line AF22 Figure 2 Testis Figure 3 Cerebral cortex Figure 4 Parathyroid gland Figure 5 Colon Figure 6 Kidney Figure 7 RNA cell line category: Cell line enhanced (hTERT-RPE1, HUVEC TERT2, NTERA-2, SuSa, U-87 MG)

Recombinant Antibody

  • Application
  • ELISA, FC, Inhib, Cell-uptake
  • Product Type
  • Ab-Fc-EVs
  • Antibody Quantification (Ab/EV)
  • ~100 Ab/EV
  • Target
  • GJA1
  • 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
  • Gap junction protein alpha 1
  • Cellular Localization
  • Vesicles, Cell Junctions, Nucleoplasm
  • Introduction
  • This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. The encoded protein is the major protein of gap junctions in the heart that are thought to have a crucial role in the synchronized contraction of the heart and in embryonic development. A related intronless pseudogene has been mapped to chromosome 5. Mutations in this gene have been associated with oculodentodigital dysplasia, autosomal recessive craniometaphyseal dysplasia and heart malformations. [provided by RefSeq, May 2014]
  • Alternative Names
  • CX43, GJAL, ODD, ODDD, ODOD, SDTY3
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