Skip to main content
Fig. 1 | SpringerPlus

Fig. 1

From: Development of a fast and economical genotyping protocol for bovine leukocyte adhesion deficiency (BLAD) in cattle

Fig. 1

T-ARMS-PCR based genotyping of BLAD. The outer primers (OF and OR) amplified a 354 bp product. The inner forward primer can detect normal allele (adenine) at position 383rd of CD18 gene with an amplicon size of 179 bp while inner reverse primer can detect mutated allele (guanine) at the same position with an amplicon size of 230 bp (lanes 13, 14, 15 and 17)

Back to article page