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. Author manuscript; available in PMC: 2009 Jun 22.
Published in final edited form as: Biochim Biophys Acta. 2007 Dec 3;1779(1):17–27. doi: 10.1016/j.bbagrm.2007.11.005

Table 1.

sEH transcription and expression and transfection efficiency in human cell lines

Cell Line Ref. Origin Disease sEH specific activity (pmol/min/mg)a Relative EPHX2 mRNA (EPHX2/GAPDH)a Renilla luciferase activitya (RLU/1×104 cells)b
HepG2 [44] liver carcinoma 310±50 0.18±0.03 600±30
HuH-7 [41] 940±40 0.99±0.20 130±30

293T [39] kidney nonec 210±10 0.54±0.08 98000±11000
ACHN [42] adenocarcinoma 31±15 0.38±0.04 30±20
SN12C [43] carcinoma n.d.d 0.08±0.02 240±60

Caco-2 [38] colon adenocarcinoma 120±10 0.33±0.02 780±70
SW480 [37] 130±30 0.68±0.08 7000±700

DU 145 [36] prostate carcinoma 440±10 0.39±0.03 9500±400

HeLa [40] cervix adenocarcinoma 52±15 0.14±0.05 3400±200
a

The control pRL-CMV plasmid contains a luciferase gene from Renilla reniformis under the control of a CMV promoter.

b

Values are mean ± SD from three different experiments.

c

Human cell line, derived from embryo kidney, expressing SV40 large T antigen abundantly.

d

n.d. indicates not detectable under the condition of our assay.