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. 2018 Jan 16;18:2. doi: 10.1186/s12896-018-0414-5

Table 1.

Table of proteins showing the highest increase in abundance in young (n = 7) and old (n = 6) tenocyte-derived constructs, according to fold change

Highest mean condition Accession (human) Protein description Function Peptide count Fold change ANOVA (p value)
TEC derived from old cells O94875 Sorbin and SH3 domain containing protein 2 Actin filament organization 10 5,1 0,02
V9HWA5 Calponin 1 Actin binding, calmodulin binding 4 3,6 0,02
P02461 Collagen type III alpha 1 ECM Collagen 38 3,5 0,01
O43294 Transforming growth factor beta induced protein ECM Glycoprotein 3 3,2 0,04
Q05707 Collagen type XIV alpha 1 ECM Collagen 3 3,0 0,02
P08123 Collagen type I alpha 2 ECM Collagen 48 3,0 0,00
Q8WX93 Palladin, cytoskeletal associated protein Enzyme 20 3,0 0,02
TEC derived from young cells Q99623 Prohibitin 2 Transcription regulator 2 3,9 0,05
P05106 Integrin beta 3 Transmembrane receptor 2 2,8 0,01
P11166 Solute carrier family 2 member 1 Transporter 3 2,2 0,02
P07919 Cytochrome b-c1 complex subunit 6 Enzyme 2 2,1 0,05
P07093 Serpin family E member 2 ECM Regulator 3 2,1 0,04
P08648 Integrin alpha 5 Transmembrane receptor 2 2,1 0,02
P30049 ATP synthase subunit delta, mitochondrial Enzyme 5 2,0 0,04

Only proteins with ≥2 unique peptides and p < 0.05 were presented. Abundant proteins in each group are also highlighted in Additional file 1