Anti-PS ADCC Enhanced Antibody (PGN635) is an ADCC enhanced antibody produced by our Afuco™ platform. PGN635 is a novel monoclonal antibody that binds PS. PGN635 may be a useful new imaging probe for detection and therapy for tumor.
Figure 7 Radioiodination does not affect binding of PGN635 F(ab’)2 to PS.
A) Competition ELISA shows 125I- PGN635 F(ab')2 and unlabeled PGN635 F(ab')2 have similar ability to compete with PGN635-biotin for binding to immobilized PS. B) Binding of ̶¹²⁴I-PGN635 F(ab')2 to PS-expressing cells. PS-exposure on ABAE and PC3-luc cells was induced by irradiation with 5 Gy 24 h before the binding assay. Non-irradiated cells served as controls. The cells were incubated with ̶¹²⁴I-PGN635 F(ab')2 or ̶¹²⁴I-control F(ab')2 for 1 h. The cells were then washed and dissolved in NaOH (1N) and 124I was quantified by gamma counting (CPM = counts/min.). Points and histograms, means; bars, + S.D.
Stafford, J. H., Hao, G., Best, A. M., Sun, X., & Thorpe, P. E. (2013). Highly specific PET imaging of prostate tumors in mice with an iodine-124-labeled antibody fragment that targets phosphatidylserine. PLoS one, 8(12), e84864.
Figure 8 ¹²⁵I-PGN635 F(ab’)2 biodistribution.
Mice (n =3) bearing s.c. PC3-luc tumors were injected with 1.85 MBq (50 µg) of ¹²⁵I-PGN635 F(ab')2 or ¹²⁵I-control F(ab')2. Antibody distribution to the indicated organs was determined after 48 h by counting the radioactivity with a gamma counter. A) Biodistribution by percent injected dose per gram (%ID/g) of tissue. B) Biodistribution by percent injected dose per organ (%ID/organ). The % ID in the blood was calculated assuming a blood volume of 2.18ml/25 g body weight.
Stafford, J. H., Hao, G., Best, A. M., Sun, X., & Thorpe, P. E. (2013). Highly specific PET imaging of prostate tumors in mice with an iodine-124-labeled antibody fragment that targets phosphatidylserine. PLoS one, 8(12), e84864.
Figure 9 ¹²⁴I-PGN635 F(ab’)2 localization predicts tumor response to therapy.
A) Mice bearing PC3-luc tumors were treated with 10 mg/kg docetaxel (CTx) or their tumors were irradiated with 15 Gy (RTx). After 24 h, the mice were injected with ¹²⁴I-PGN635 F(ab')2 and imaged by PET 48 h later. B) CTx and RTx significantly inhibited tumor growth (one-way ANOVA, P < 0.01). C) ¹²⁴I-PGN635 F(ab')2 uptake was significantly higher in treated tumors (one-way ANOVA, P < 0.05). D) The tumor-to-normal (T/N) ratio inversely correlated with the tumor growth over the next 28 days (Pearson's r = -0.85, P < 0.01). The tumor volume on day 28 was divided by the volume on the day of treatment to calculate the fold change in tumor volume. The T/N ratio at the time of imaging was predictive of the tumor response.
Stafford, J. H., Hao, G., Best, A. M., Sun, X., & Thorpe, P. E. (2013). Highly specific PET imaging of prostate tumors in mice with an iodine-124-labeled antibody fragment that targets phosphatidylserine. PLoS one, 8(12), e84864.
This is a product of Creative Biolabs' Hi-Affi™ recombinant antibody portfolio, which has several benefits including:
• Increased sensitivity
• Confirmed specificity
• High repeatability
• Excellent batch-to-batch consistency
• Sustainable supply
• Animal-free production
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FAMAB-0255-YC-S(P) | Mouse Anti-PS Recombinant Antibody (clone PS4A7); scFv Fragment | ELISA | Mouse scFv |
FAMAB-0256-YC-S(P) | Mouse Anti-PS Recombinant Antibody (clone PS3A); scFv Fragment | ELISA | Mouse scFv |
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HPAB-1899-FY-F(E) | Mouse Anti-PS Recombinant Antibody; Fab Fragment (HPAB-1899-FY-F(E)) | ELISA, Inhib | Mouse Fab |
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