Recombinant Anti-CD40 (CRD2 x CRD1) Biparatopic Antibody, Tandem scFv (CAT#: VS-0525-YC206)

This biparatopic antibody (bpAb) targets two distinct CD40 epitopes via its tandem scFv arms, which bind simultaneously with high affinity. One scFv targets an epitope on both CRD2 and CRD1, directly overlapping with the CD40L binding site. In contrast, the other scFv targets an epitope on the top half of CRD1, notably not overlapping with the CD40L binding interface.

Specific Inquiry
  • Gene Expression
  • Datasheet
  • MSDS
  • COA
Normal Tissue
RNA Expression

Specifications

  • Host Animal 1
  • Human
  • Host Animal 2
  • Mouse
  • Specificity
  • Human CD40
  • Species Reactivity
  • Human
  • Type
  • Tandem scFv
  • Valency
  • 1 + 1
  • Epitope 1
  • Both CRD2 and CRD1, exactly overlapping with the CD40L binding site.
  • Epitope 2
  • The top half of CRD1, and no overlap with the CD40L binding interface
  • Purity
  • >90%
  • Purification
  • Affinity purified
  • Applications
  • ELISA, FC, IF, IHC, IP
  • Concentration
  • Lot specific
  • Buffer
  • PBS, pH 7.4
  • Preservative
  • No preservatives
  • Storage
  • Store at 4°C for short term. Aliquot and store at -20°C for long term. Avoid freeze-thaw cycles.
  • Long Name
  • CD40 Molecule

Target

  • Introduction
  • This gene is a member of the TNF-receptor superfamily. The encoded protein is a receptor on antigen-presenting cells of the immune system and is essential for mediating a broad variety of immune and inflammatory responses including T cell-dependent immunoglobulin class switching, memory B cell development, and germinal center formation. AT-hook transcription factor AKNA is reported to coordinately regulate the expression of this receptor and its ligand, which may be important for homotypic cell interactions. Adaptor protein TNFR2 interacts with this receptor and serves as a mediator of the signal transduction. The interaction of this receptor and its ligand is found to be necessary for amyloid-beta-induced microglial activation, and thus is thought to be an early event in Alzheimer disease pathogenesis. Mutations affecting this gene are the cause of autosomal recessive hyper-IgM immunodeficiency type 3 (HIGM3). Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported.
  • Alternative Names
  • Tumor necrosis factor receptor superfamily member 5; TNFRSF5; p50

Related Resources

  • Related Diseases

Downloads

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For Research Use Only. Not For Clinical Use.

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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