Table 1. Three selected hybridoma clones to convert stable cMAbs against BP and BM.
cMAb ID | 3 selected hybridomas converted into cMAbsa | Chimeric chain IDb | ||||
Hybridoma clone ID | Antigen injected | Isotype | Cross-reactivity | Heavy(mVH+HcG1) | Light(mVL+HcK) | |
cMAb CK1 | BP7 10B11 | BP 430 | IgG1/κ | BP/BM: +; BT: − | H1 | L1 |
cMAb CK2 | BP7 2C6 | BP 430 | IgG2a/κ | BP/BM: +; BT: − | H2 | L2 |
cMAb CK3 | BP1 7F7 | BP 8324 | IgG3/κ | BP/BT: +; BM: − | H3 | L3 |
aThese 3 hybridoma clones were selected by their binding specificities, antigen reactivities to their bacterial cell components, and in vitro/vivo neutralizing activities against B. pseudomallei (BP) 8324 and/or B. mallei (BM) ATCC 23344. BT: B. thailandensis.
bEach chimeric chain was assembled by the overlapping PCR. mVH: mouse variable heavy chain; HcG1: human constant gamma 1; mVL: mouse variable light chain; HcK: human constant kappa chain.