Gene probe-based detection of type E botulinum neurotoxin binding protein using polymerase chain reaction
Using primers based on the nucleotide sequence of a neurotoxin binding protein from Type E Clostridium botulinum cultures, an amplified DNA product was obtained through polymerase chain reaction. The 400 base pair amplified DNA fragment was detectable with as low as 0.1 pg template DNA from Type E C...
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Veröffentlicht in: | Toxicon (Oxford) 1996-07, Vol.34 (7), p.737-742 |
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