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. 2016 Dec 1;5(11):560–568. doi: 10.1302/2046-3758.511.BJR-2016-0033.R3

Table III.

Overview of successful analysis of gene expression

RNA isolation kit Homogenisation method Articular cartilage
Meniscus
Annulus fibrosus
Nucleus pulposus
COL2A1 ACAN COL2A1 ACAN COL2A1 ACAN COL2A1 ACAN
TRIzol MagNA 6/6 6/6 6/6 6/6 6/6 6/6 2/6 2/6
Freezer 6/6 6/6 4/6 5/6 5/6 5/6 4/6 4/6
Lipid MagNA 6/6 6/6 6/6 6/6 6/6 6/6 6/6 6/6
Freezer 6/6 6/6 6/6 6/6 6/6 6/6 6/6 6/6
Fibrous MagNA 6/6 6/6 6/6 6/6 6/6 6/6 6/6 6/6
Freezer 6/6 6/6 2/6 2/6 6/6 6/6 6/6 6/6
Aurum MagNA 5/6 6/6 6/6 6/6 6/6 6/6 3/6 3/6
Freezer 6/6 6/6 2/6 2/6 5/6 5/6 5/6 5/6

Real-time polymerase chain reaction analysis was performed for all samples to validate the quality of the isolated RNA. Numbers indicate the total of quantifiable samples. Samples were obtained from three goats. Per goat, two duplicate samples were run independently for both homogenisation methods and for the four different methods of RNA extraction

RNA, ribonucleic acid; COL2A1, collagen type II; ACAN, aggrecan; MagNA, MagNA Lyser; Freezer, Freezer Mill