Antibody Information
General Information of This Antibody
| Antibody ID | ANTI0RLSLW |
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| Antibody Name | B9 |
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| Organization | Fudan University.; University of Auckland,.; Shanghai Engineering Research Center for Synthetic Immunology. |
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| Synonyms |
B9
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| Antibody Type | Monoclonal antibody (mAb) |
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| Antigen Name | Carcinoembryonic antigen-related cell adhesion molecule 5 (CEACAM5) |
Antigen Info | ||||
| Click to Show/Hide the Sequence Information of This Antibody | ||||||
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
| Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
25.6 nM
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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
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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
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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
