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. Author manuscript; available in PMC: 2009 Apr 13.
Published in final edited form as: Nat Methods. 2008 Apr 13;5(5):393–395. doi: 10.1038/nmeth.1201

Table 1.

Optimized electroporation conditions

Pulse intensity (V/cm) Pulse duration (ms) Pulse number Transfection efficiencya (%) Cell deathb (%)
HL-60c (cDNAd) 670 20 1 45 40−45
HL-60c (siRNAe) 630 7 2 90 5−10
Hippocampal neurons (cDNAd) 530 15 1 ∼ 50 50−60
HUVEC (cDNAd) 530 15 1 65 60−70
3T3-L1c (cDNAd) 470 20 1 55 40−50
RBL-2H3 (cDNAd) 670 15 1 45 40−45
a

Number of electroporated live cells/number of total live cells.

b

Determined by comparing the number of live cells between treated versus non-treated samples in which the same amount of cells were pipetted.

c

Differentiated cells.

d

Optimized conditions for eGFP cDNA at a concentration of 25−10 ng/μl in extracellular buffer.

e

Optimized conditions for LMNA siRNA at a concentration of 750−500 nM in extracellular buffer. Data shown for HL-60 cells, hippocampal neurons and HUVECs are averages from n = 8−10 experiments; for 3T3-L1 and RBL-2H3 cells, n = 3.