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. 2018 Feb 8;17(4):5571–5580. doi: 10.3892/mmr.2018.8584

Table I.

The experimental design of CyDye labelling for each individual retinal paired sample (n=5).

Gel no. Cy2 dye (internal control) Cy3 dye Cy5 dye
Gel 1 Pool of all 10 eyes Treated 1 Control 1
(5 µg from each sample) (50 µg) (50 µg)
Gel 2 Pool of all 10 eyes Control 2 Treated 2
(5 µg from each sample) (50 µg) (50 µg)
Gel 3 Pool of all 10 eyes Treated 3 Control 3
(5 µg from each sample) (50 µg) (50 µg)
Gel 4 Pool of all 10 eyes Control 4 Treated 4
(5 µg from each sample) (50 µg) (50 µg)
Gel 5 Pool of all 10 eyes Treated 5 Control 5
(5 µg from each sample) (50 µg) (50 µg)

A total of 50 µg treated and un-treated control eyes were labelled with different dyes (Cy3 or Cy5 randomly). A total of 150 µg labelled proteins (treated, control and pooled standard) were loaded on each gel (gel 1-gel 5) for 2D difference gel electrophoresis run.