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. 2011 May 9;6(5):e19867. doi: 10.1371/journal.pone.0019867

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.