General Information of This Antibody
Antibody ID
ANTI0RLSLW
Antibody Name
B9
Organization
Fudan University.; University of Auckland,.; Shanghai Engineering Research Center for Synthetic Immunology.
Synonyms
B9
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Antibody Type
Monoclonal antibody (mAb)
Antigen Name
Carcinoembryonic antigen-related cell adhesion molecule 5 (CEACAM5)
 Antigen Info 
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Each Antibody-drug Conjugate Related to This Antibody
Full Information of The Activity Data of The ADC(s) Related to This Antibody
B9-MMAE [Investigative]
Revealed Based on the Cell Line Data
Click To Hide/Show 3 Activity Data Related to This Level
Experiment 1 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal inhibitory Concentration (lC50)
25.6 nM
Low CEACAM5 expression (CEACAM5+)
Method Description
Logarithmically growing cell lines MKN-45, BxPC-3, LS174T, and FCHO were seeded in a 96 well cell culture plate at 5000 cells/well for 12 h. After the culture supernatant was discarded, the 200 uL three-fold diluted UdADC was added to cells, with native antibody B9 and free payload vcMMAE used as control. The concentration of each group started from 1 uM and was repeated in triplicate. Cells were cultured for 72 h at 37 °C, then the culture medium was removed and 100 uL CCK8 solution (10 uL CCK8 + 90 uL medium) was added into each well, using CCK8 solution without cells as reference wells. After cells were incubated at 37 °C for 1-3 h, absorbance was measured at 450 nm using a 96-well microplate reader. Cell viability (%) = [ (ODtreated - ODreference well)/ (ODnon-treated - ODreference well)] × 100%.

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In Vitro Model Pancreatic ductal adenocarcinoma BxPC-3 cells CVCL_0186
Experiment 2 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal inhibitory Concentration (lC50)
38.14 nM
High CEACAM5 expression (CEACAM5 +++)
Method Description
Logarithmically growing cell lines MKN-45, BxPC-3, LS174T, and FCHO were seeded in a 96 well cell culture plate at 5000 cells/well for 12 h. After the culture supernatant was discarded, the 200 uL three-fold diluted UdADC was added to cells, with native antibody B9 and free payload vcMMAE used as control. The concentration of each group started from 1 uM and was repeated in triplicate. Cells were cultured for 72 h at 37 °C, then the culture medium was removed and 100 uL CCK8 solution (10 uL CCK8 + 90 uL medium) was added into each well, using CCK8 solution without cells as reference wells. After cells were incubated at 37 °C for 1-3 h, absorbance was measured at 450 nm using a 96-well microplate reader. Cell viability (%) = [ (ODtreated - ODreference well)/ (ODnon-treated - ODreference well)] × 100%.

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In Vitro Model Gastric adenocarcinoma MKN-45 cells CVCL_0434
Experiment 3 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal inhibitory Concentration (lC50)
101.4 nM
High CEACAM5 expression (CEACAM5 +++)
Method Description
Logarithmically growing cell lines MKN-45, BxPC-3, LS174T, and FCHO were seeded in a 96 well cell culture plate at 5000 cells/well for 12 h. After the culture supernatant was discarded, the 200 uL three-fold diluted UdADC was added to cells, with native antibody B9 and free payload vcMMAE used as control. The concentration of each group started from 1 uM and was repeated in triplicate. Cells were cultured for 72 h at 37 °C, then the culture medium was removed and 100 uL CCK8 solution (10 uL CCK8 + 90 uL medium) was added into each well, using CCK8 solution without cells as reference wells. After cells were incubated at 37 °C for 1-3 h, absorbance was measured at 450 nm using a 96-well microplate reader. Cell viability (%) = [ (ODtreated - ODreference well)/ (ODnon-treated - ODreference well)] × 100%.

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In Vitro Model Colon adenocarcinoma LS174T cells CVCL_1384
References
Ref 1 A novel human single-domain antibody-drug conjugate targeting CEACAM5 exhibits potent in vitro and in vivo antitumor activity