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. 1996 Nov 26;93(24):13979–13984. doi: 10.1073/pnas.93.24.13979

Table 2.

Transgene mutations in PCR clones derived from anti-phOx hybridomas

Hybridoma Antibody
No. of PMs per copy*
Cκ, rat Cκ, mouse ΔBWT ΔBWTm ΔBM7 WT M7 ΔBTCAM7
LκNG
 C15.2.7 +  8  and 6 7  3 and 3
 C10.5.4 +  5  and 8 6  1 and 1
 A6.8 +  3  and 3 1 0
 C23.1.5 +  7  and nf NF  2 and 2
 D1.1.5 + 10  and 0 NF 10 and 0
 B20.6 +  4  and 0 2  4 and 0
 C6.3.6 +  8  and nf 4  5 and 2
 D12.3.8 + 0 2 0
 C4.6.8 + 0 2 0
 D23.4 +  1  and 0 1  1 and 0
LκWTM7
 D3.3.3 + 3§ 7
 C12.1.3 + 5§ 7
 EH2.5 ± + 0 4
 RB3.6 ± + 0 3
 EA8.7 ± + 0 1
 C3.23.2 ± + 0 0
 C11.4.8.8 + 0 0
LκΔBTCAM7/ΔLi
 B2.4.4 + 3
 C14.1.9 + 6
 A20.5.2 + 4

PM, point mutation; NF, not found. 

*

Number of PMs found in each transgenic copy. 

This copy was identified by a silent substitution (G for A) in codon Lys-18. 

Copies containing the critical mutation of His-34 to Asn or Gln. In addition, all of them included the mutation Tyr-36 to Phe. 

§

These copies also carried deletions that result in a coding sequence out of frame.