Recombinant Anti-L1CAM Vesicular Antibody, EV Displayed (VS-0425-YC318)

CAT#: VS-0425-YC318

The Recombinant Anti-L1CAM Vesicular Antibody, EV Displayed (VS-0425-YC318) 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 L1CAM-expressed cells or tissues. The L1CAM is an axonal glycoprotein that is crucial for neuronal development, with mutations leading to neurological syndromes like CRASH.

Gene Expression
Figure 1 IF staining of human cell line U-2 OS Figure 2 IF staining of human cell line A-431 Figure 3 IF staining of human cell line U-251 MG Figure 4 Cerebral cortex Figure 5 Colon Figure 6 Kidney Figure 7 RNA cell line category: Cell line enhanced (BJ hTERT+, BJ hTERT+ SV40 Large T+ RasG12V, HeLa, RH-30, RPTEC TERT1)

Recombinant Antibody

  • Application
  • ELISA, FC, Cell-uptake
  • Product Type
  • Ab-Fc-EVs
  • Antibody Quantification (Ab/EV)
  • ~100 Ab/EV
  • Target
  • L1CAM
  • Host Animal
  • Mouse
  • Antibody Isotype
  • IgG
  • 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
  • L1 cell adhesion molecule
  • Biological Process
  • Cell adhesion, Differentiation, Neurogenesis
  • Molecular Function
  • Developmental protein
  • Cellular Localization
  • Nucleoplasm, Plasma membrane
  • Introduction
  • The protein encoded by this gene is an axonal glycoprotein belonging to the immunoglobulin supergene family. The ectodomain, consisting of several immunoglobulin-like domains and fibronectin-like repeats (type III), is linked via a single transmembrane sequence to a conserved cytoplasmic domain. This cell adhesion molecule plays an important role in nervous system development, including neuronal migration and differentiation. Mutations in the gene cause X-linked neurological syndromes known as CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus).
  • Alternative Names
  • CAML1, CD171, HSAS, HSAS1, MASA, MIC5, NCAM-L1, S10, SPG1
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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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