Figure 2 | Scientific Reports

Figure 2

From: Molecular basis of the scalp-ear-nipple syndrome unraveled by the characterization of disease-causing KCTD1 mutants

Figure 2

Gel filtration elution profiles of KCTD1, KCTD1BTB, KCTD1CTD (A) and of the SEN-causing mutants KCTD1P20S, KCTD1H33P, KCTD1G62D, KCTD1D69E, KCTD1H74P (B). The MW markers used for reference are: blue dextran 2000 (Mw > 1000 kDa, retention volume 7.8 mL), ovalbumin (Mw 43 kDa, retention volume 14.9 mL), carbonic anhydrase (Mw 29 kDa, retention volume 15.6 mL), and ribonuclease A (Mw 13.7 kDa, retention volume 17.2 mL).

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