Anti-HRAS Antibody Prodrug, Protease Activated (CBH03YJ)

CAT#: VS-1025-YC23

The Anti-HRAS Antibody Prodrug, Protease Activated (CBH03YJ) is an antibody prodrug comprised of a recombinant mouse antibody targeting human HRAS, linked to a masking peptide that conceals the active antigen-binding site via a protease-cleavable linker. The mask peptide is recombinantly attached to the amino terminus of either the light or heavy chain of the antibody, designed to block access to the antigen-binding site and physically prevent the antibody from binding to HRAS protein. Once the masking peptide is cleaved by matrix metalloproteinases (MMPs), the prodrug is activated, allowing the unmasked monoclonal antibody component to bind to HRAS effectively. HRAS is a small GTPase and one of the three RAS family members that act as a central hub in numerous signaling pathways regulating cell growth. Activating point mutations in the HRAS gene are found in a variety of tumors, particularly those of the urinary tract and head and neck. These mutations lock the protein in its active state, driving continuous, oncogenic signaling.

Gene Expression
Figure 1 IF staining of human cell line MCF7 Figure 2 IHC staining of human rectum Figure 3 Cerebral cortex Figure 4 Colon Figure 5 Gallbladder Figure 6 Lymph node Figure 7 RNA cell line category: Low cell line specificity

Specifications

  • Host Animal
  • Mouse
  • Applications
  • In situ zymography (ISZ), Cytotoxicity assay (Cyt), Functional assay
  • Specificity
  • Human HRAS
  • Target
  • HRAS
  • Species Reactivity
  • Human
  • Isotype
  • IgG
  • Clone
  • CBH03YJ
  • Masking Approach
  • Affinity mask
  • Mask
  • A synthetic peptide
  • Protease Cleavable Linker
  • MMP-cleavable linker
  • Protease Substrate
  • MMPs
  • Purification
  • Protein A purified
  • Buffer
  • PBS, pH 7.4
  • Preservative
  • No preservatives
  • Storage
  • Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Target

  • Introduction
  • HRAS belongs to the Ras oncogene family, whose members are related to the transforming genes of mammalian sarcoma retroviruses. The products encoded by these genes function in signal transduction pathways. These proteins can bind GTP and GDP, and they have intrinsic GTPase activity. P21ras undergoes a continuous cycle of de- and re-palmitoylation, which regulates its rapid exchange between the plasma membrane and the Golgi apparatus. Mutations in HRAS cause Costello syndrome, a disease characterized by increased growth at the prenatal stage, growth deficiency at the postnatal stage, predisposition to tumor formation, cognitive disability, skin and musculoskeletal abnormalities, distinctive facial appearance and cardiovascular abnormalities. Defects in HRAS are implicated in a variety of cancers, including bladder cancer, follicular thyroid cancer, and oral squamous cell carcinoma.
  • Alternative Names
  • CTLO; KRAS; HAMSV; HRAS1; KRAS2; RASH1; RASK2; Ki-Ras; p21ras; C-H-RAS; c-K-ras; H-RASIDX; c-Ki-ras; C-BAS/HAS; C-HA-RAS1; GTPase HRas; GTP- and GDP-binding peptide B
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