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. 2003 Oct;69(10):5875–5883. doi: 10.1128/AEM.69.10.5875-5883.2003

TABLE 2.

Cross-reactivity in reverse line blot hybridization of probes to control templates with few mismatches

Probe and clone Target sequence Cross- reactivityb
Probe Rho-BAL47-396 CATTCCGCGTGCAGGA
    Clone URK0-13 ---G------------
    Clone Sta5-10 ---G------------
    Clone LD2 ---C------------
    Clone Med0-02 ---C------------
    Clone LD3 ---G--A---------
    Clone LD21 ---C-------A----
    Clone LD1 ---C-------G----
    Clone URK0-17 ---G--------G---
Probe Rpickettii-490 GGAAGAATAAGGACCGGCT
    Clone LD17 T----------C-------
    Clone LD3 T------------T-----
    Clone URK0-13 -T-----------T-----
Probe CR-FL23-464a TAACACAG•CTGTGAAUGACGG
    Clone LD17 --------T-------------
Probe Sta230-187 GCATCACTGAGTTTTGAAAGAATT
    Clone Sta5-26 -----G------------------ +
Probe Urk014-126 GAGAAACCAACCCCGGTC
    Clone Sta2-06 --------TG---T----
Probe Syn/Pro-415 AGGCCTCTGGGCTGTAAAC
    Clone LD6 ------G----T-------
    Clone URK0-03 ------TC-----------
    Clone MED0-06 ------TC-----------
a

Probe CR-FL23-464 and clone LD17 differ by an insertion or deletion as indicated by the bullet.

b

That is, the presence (+) or absence (−) of reactivity of probes to the mismatching templates (0.2 pmol of PCR product [F27-R518] per slot).