Anti-Tissue factor (TF-011)-vc-MMAE ADC (HuMax-TF ADC) (CAT#: ADC-L015)

This ADC product is composed of an anti-Tissue factor antibody (clone TF-011) conjuagated via a vc linker to MMAE (TF-011-vc-MMAE). It has demonstrated a response in Prostate cancer treatment by a MOA (Mechanism of Action) of Depolymerize Microtubules.

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

Specifications

  • Antibody Overview
  • Fully human IgG1K monoclonal antibody that binds to TF
  • Clone
  • TF-011
  • Antibody Conjugation
  • Human
  • Linker
  • vc (valine-citrulline)
  • Linker Class/Description
  • Class: Enzymatically cleavable linkers-Peptide linkers
    Description: peptide linkers, belonging to Enzymatically cleavable linkers, combine greater systemic stability with rapid enzymatic release of the drug in the target cell. The scission of peptidic bonds relies on lysosomal proteolytic enzymes, which have very low activities in blood due to endogenous inhibitors and the unfavorably high pH value of blood.
  • Drug
  • MMAE (Monomethyl auristatin E)
  • Drug Class/Description
  • Auristatins are water-soluble dolastatin analogs of dolastatin 10. Dolastatin 10 belongs to dolastatin family and it can powerfully bind to tubulin, thus inhibiting polymerization mediated through the binding to the vinca alkaloid binding domain, and causes cell to accumulate in metaphase arrest.

Target

  • Introduction
  • Tissue factor (TF), formerly known as thromboplastin, is the key initiator of the coagulation cascade; it binds factor VIIa resulting in activation of factor IX and factor X, ultimately leading to fibrin formation.
  • Alternative Names
  • TF; Tissue factor

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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