Recombinant Anti-NOTCH1 (LBD domain x HD-LNR domain) Biparatopic Antibody, Tandem scFv (Clone hN1wc49 x Clone N1wc104) (CAT#: VS-0525-YC139)

The Recombinant Anti-NOTCH1 (LBD domain x HD-LNR domain) Biparatopic Antibody, Tandem scFv (Clone hN1wc49 x Clone N1wc104) is a biparatopic antibody (bpAb) that recognizes two distinct epitopes of NOTCH1. The bpAb's tandem scFv design fuses the hN1wc49 scFv (targeting the ligand binding domain, LBD, of human Notch1) N-terminally to the N1wc104 scFv (specific for the HD-LNR domain of human Notch1).

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

Specifications

  • Host Animal 1
  • Human
  • Host Animal 2
  • Human
  • Specificity
  • Human NOTCH1
  • Species Reactivity
  • Human
  • Type
  • Tandem scFv
  • Valency
  • 1 + 1
  • Clone 1
  • hN1wc49
  • Clone 2
  • N1wc104
  • Epitope 1
  • Ligand Binding Domain (LBD)
  • Epitope 2
  • HD-LNR domain
  • Purity
  • >90%
  • Purification
  • Affinity purified
  • Applications
  • ELISA
  • 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
  • Notch 1

Target

  • Introduction
  • Notch 1 is a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor plays a role in the development of numerous cell and tissue types. Mutations in this gene are associated with aortic valve disease, Adams-Oliver syndrome, T-cell acute lymphoblastic leukemia, chronic lymphocytic leukemia, and head and neck squamous cell carcinoma.
  • Alternative Names
  • Notch 1; Translocation-Associated Notch Protein TAN-1; TAN1; HN1; Notch (Drosophila) Homolog 1 (Translocation-Associated); Notch Homolog 1, Translocation-Associated (Drosophila); Notch Homolog 1, Translocation-Associated

Related Resources

  • Related Diseases

Downloads

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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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