ELISAs were used to detect FIV infection.
Centromere probes were used to detect chromosomal aneusomy of chromosomes 3, 7, 9, and 15.
Frozen sections of 10 μm were used to detect R-Ras expression.
Routine Western blotting procedures were used to detect protein content as described10.
5′-TTACTGACCGTACACCAAATTTGCCTGC-3′ and 5′-CCTGGCAGCGATCGCTATTTTCCATGAGTG-3′ were used to detect Cre recombinase (450 bp).
Partek GSA were used to detect differential expressed genes between treated vs not treatment groups.
Immunoprecipitation and western blot analysis were used to detect MyD88s protein expression as indicated by the arrow (27 kDa) (g).
(a d) Flow cytometry and the fluorogenic probe MitoSOX22 were used to detect mitochondrial superoxide in SiHa cells.
Approximately 85.5% of the trimmed reads were aligned to a single genomic location, and were used to detect SNPs.
Amplimers 5′-AGGATTTATGCCCTCTGCTTGTC-3′ and 5′-GAACCACTGTTCCAATTTCCATCC-3′ were used to detect Jnk1+ (540 bp) and Jnk1LoxP (330 bp) alleles.
Amplimers 5′-CCTCAGGAAGAAAGGGCTTATTTC-3′ and 5′-GAACCACTGTTCCAATTTCCATCC-3′ were used to detect Jnk1LoxP (1000 bp) and Jnk1∆ (410 bp) alleles.
