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Hi everyone, I have got this question for you. I have been working on a sheep lactoalbumin (LALBA) gene to seek for polymorphism via PCR-RFLP. My sequence has been digested by several enzymes (by...
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Primers were designed for LALBA gene based on coding squence (Exon 5) and for RFLP PCR product was cut EcoRI. We have only seen two digested DNA bands on agaraose gel for 65 animals upon genotyping?
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