1. Apoptosis
  2. Apoptosis
  3. Citatuzumab bogatox

Citatuzumab bogatox  (Synonyms: VB6-845; Anti-Human EpCAM Recombinant Antibody Fab Fragment, 17-1A)

Cat. No.: HY-P99282
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Citatuzumab bogatox (VB6-845) is recombinant immunotoxin that composed of Fab fragment of humanized antibody targeting EpCAM and a modified cytotoxin bouganin. Citatuzumab bogatox binds to and selectively induces apoptosis in EpCAM-positive cell lines and shows good activity in EpCAM-positive human tumour xenograft models.

For research use only. We do not sell to patients.

CAS No. : 945228-49-9

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Description

Citatuzumab bogatox (VB6-845) is recombinant immunotoxin that composed of Fab fragment of humanized antibody targeting EpCAM and a modified cytotoxin bouganin. Citatuzumab bogatox binds to and selectively induces apoptosis in EpCAM-positive cell lines and shows good activity in EpCAM-positive human tumour xenograft models[1][2][3].

In Vitro

Citatuzumab bogatox (0-100 nM; 5 days) inhibits growth of NIH:OVCAR-3 and CAL-27 cells, with IC50s both are 3 nM[1].
Citatuzumab bogatox internalizes into the cytoplasm of EpCAM-expressing cells and then the released Bouganin inhibits protein synthesis by inactivation of ribosome and leading to apoptosis of the cancer cells[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[1]

Cell Line: NIH:OVCAR-3 and CAL-27 cells
Concentration: 0-100 nM
Incubation Time: 5 days
Result: Exhibited an IC50 of 3 nM to against the EpCAM-positive cell lines.
In Vivo

Citatuzumab bogatox (10, 20 mg/kg; i.v./i.p.) inhibits growth of tumor in mice[1].
Citatuzumab bogatox (10, 20 mg/kg) are well tolerated by mice without any significant weight loss[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Female CB.17 SCID mice (~20 g; OVCAR-3 Xenograft model)[1].
Dosage: 10, 20 mg/kg
Administration: Tail vein (until day 26 when due to tail swelling, route of administration was changed to intraperitoneal for the remaining 7 doses); single daily for 5 consecutive days for 3 weeks and then received maintenance dosing on Monday and Friday for 4 weeks.
Result: Showed an average of 40 mm3 (control group was 750 mm3) on day 75, and with 3/15 mice being tumor free, when at 10 mg/kg.
Almost completely inhibited tumour growth when at 20 mg/kg.
CAS No.
SMILES

[Citatuzumab bogatox]

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Format
  • Fab-G1-kappa
Purity & Documentation
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Citatuzumab bogatox
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