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Table 1 Maturation-inducing and steroidogenic activities in active fractions derived from a combination of chromatofocusing followed by HICa

From: Fundulus heteroclitus gonadotropins.5: Small scale chromatographic fractionation of pituitary extracts into components with different steroidogenic activities using homologous bioassays

  

pg per well

X 100

Sample

GVBD (%)

E2

T

DHP

T/E2

DHP/E2

FPE b

38 ± 7

5,850 ± 2,000

264 ± 48

332 ± 68

4.5

5.7

FPE c

40 ± 5

4,450 ± 2,000

240 ± 56

312 ± 48

5.4

7.0

I-1 d

12 ± 12

3,150 ± 1,204

147 ± 53

126 ± 18

4.7

4.0

II-8 d

29 ± 8

3,300 ± 450

145 ± 14

139 ± 49

4.4

4.2

III-10 d

4 ± 3

2,120 ± 701

60 ± 60

43 ± 15

2.8

2.0

V-19 d

26 ± 15

4,483 ± 393

271 ± 23

339 ± 91

6.0

7.6

  1. aResults presented as means ± SEM derived from three chromatographic series. In the absence of added gonadotropin, no GVBD took place and T- and DHP-production were undetectable, while E2-production averaged 1,150 pg per well. The latter baseline value was subtracted from the induced E2 data to provide the indicated values for E2. bThawed, immediately added to L-15 medium, and tested for activity at a concentration of 0.5 pit. equiv./well (0.25 pit. equiv./ml). cThawed, stored for up to a week at 4°C, dialyzed overnight against distilled water, dried by vacuum centrifugation, reconstituted with L-15 medium, and tested for activity at a concentration of 0.5 pit. equiv./well. dRoman numerals refer to portions of the chromatofocusing runs (Fig. 4) while Arabic numerals refer to active fractions found after subsequent HIC (Fig. 5).