Skip to main content

Table 2 Expression analysis of proteins.

From: Multiplexed expression and screening for recombinant protein production in mammalian cells

  

Fluorescence Intensity (×104)

  
  

50 ml culture

2 ml culture

  

Vector

Protein

Western blot

Dot blot

Ex-IMAC AKTA (µg)

Analytical SEC (µg)

#1

Mfap3

0

0

0.4

0

-

#2

CLM9

850.6

657.1

298.4

535.5

124.6

#3

Undefined

1228.5

1054.3

1516.6

833.1

526.0

#4

4732429D16Rik

0

0

15.8

0

-

#5

BC025105

19.6

56.3

9.7

0

-

#6

Fcer1a

795.9

456.0

909.6

256.0

97.8

#7

Cd2

900.6

584.5

432.2

483.1

387.2

#8

Tmem25

0

0

5.6

0

-

#9

Tmem25

0

0

6.8

0

-

#10

Tmem25

53.6

122.3

147.5

117.9

-

#11

F11r

0

0

44.4

79.3

-

#12

Ptpns1

0

0

0.2

0

-

#13

Il18rap

65.4

65.3

152.0

70.3

-

#14

Unc5b

419.7

101.9

206.0

297.3

68.6

#15

Fgfrl1

0

0

5.0

64.6

-

#16

AI415330

312.1

58.3

1081.3

191.2

-

#17

Ly9

494.6

425.5

485.9

387.5

57.6

#18

Scn3b

0

0

5.6

0

-

#19

E130306I01Rik

0

0

25.3

0

-

#20

Kit

0

0

4.2

0

-

#21

Lag3

410.7

428.6

371.1

296.8

73.1

#22

Lrrn1

182.6

90.4

117.4

131.3

-

  1. Fluorescent intensity of bands on western blot and dots on dot blots were analysed using ImageQuant software. The Ex-IMAC AKTA column values are calculated by integrating the elution peak from the sephadex column between the IMAC and ion-exchange steps. The Analytical SEC column values are calculated by analysing the purified proteins (see Methods section). There is a cut off during AKTA purification, if the imidazole strip peak detects < 200 ug the fraction is not collected and therefore no protein is purified and there is nothing to analyse on the SEC. All values are normalised to the same input volume of 50 ml for western blot, dot blot and purification analysis. Abbreviations: IMAC (Immobilised Metal Affinity Chromatography), SEC (Size Exclusion Chromatograpy).