KB-1358

IBI334-B7H3-hIgG1

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33677
Home » Antibodies » IBI334-B7H3-hIgG1

Background of IBI334-B7H3-hIgG1

EGFR is a tyrosine kinase receptor that plays a vital role in cell proliferation, differentiation, and survival through essential signaling pathways. Abnormal EGFR signaling can cause excessive cell growth and the formation of tumors. Conversely, B7-H3 is an immune checkpoint molecule that primarily inhibits the activation and expansion of T cells, thus preventing an overactive immune response. EGFR/B7-H3 dual antibodies are targeted drugs that specifically target these two molecules. They function by inhibiting EGFR signaling to impede tumor cell proliferation and by blocking B7-H3 signaling to activate T cells, thereby enhancing their ability to attack tumor cells. Consequently, the primary mechanism of action of EGFR/B7-H3 dual antibody therapy is to simultaneously inhibit tumor growth and enhance the immune system's ability to kill, resulting in a dual assault on tumors.

Specifications

Catalog NumberKB-1358
Antibody NameIBI334-B7H3-hIgG1
IsotypeHuman IgG1,kappa
TargetB7H3
Species ReactivityHuman
Host Cell LineEXPI CHO
Purification MethodAffinity purified
Concentration>2 mg/mL
Formulation50 mM sodium citrate,150mM NaCl,pH5.5
Purity>95% by SDS-PAGE and SEC-HPLC
ValidationELISA
Endotoxin Level<0.2 EU/mg as determined by the LAL method
Sterility0.2μm filtered
StorageIt is recommended that the protein should be aliquoted for optimal storage.
Avoid repeated freeze-thaw cycles.
StabilityStable for twelve months from date of receipt when stored at -20°C to -80°C;
Stored at 2-8°C for one month without detectable loss of activity.

Characterization

Application

References

  1. Next‐generation sequencing of tissue and circulating tumor DNA: Resistance mechanisms to EGFR targeted therapy in a cohort of patients with advanced non‐small cell lung cancer.
  2. Zhao Q, Liu J, Yang S. Therapeutically targeting B7-H3 via chimeric antigen receptors and bispecific killer cell engagers in non-small cell lung cancer. Journal of Immunology. 2018:200.
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