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. 2017 Mar 8;7:43833. doi: 10.1038/srep43833

Table 4. Quality and quantity of genomic DNA for genotype concordance analyses.

Sample group Blood volume (ml) DNA source −80 °C period (weeks) Cell number when thawed (×106) Viability when thawed (%) Culture period (weeks)**** Final cell number (×106) DNA yield (μg) OD260/280
#7 5 Peripheral blood* 136** 4.2 ± 1.9 1.79 ± 0.09
LCL-gradient 130*** 1.2 ± 4.9 79.2 ± 4.7 6 2.3 ± 0.4 3.2 ± 0.7 1.96 ± 0.02
LCL-hemolytic 130*** 1.1 ± 2.2 80.2 ± 5.5 6 3.0 ± 0.4 3.8 ± 1.3 1.89 ± 0.01
#8 2 Peripheral blood* 60** 3.2 ± 2.2 1.82 ± 0.03
LCL-hemolytic 52*** 0.4 ± 0.4 78.9 ± 8.3 8 2.0 ± 1.0 2.6 ± 1.2 1.93 ± 0.04
#9 0.1 Peripheral blood* 10** 3.7 ± 3.5 1.82 ± 0.04
LCL-hemolytic 0 12 0.7 ± 0.2 1.7 ± 0.6 1.88 ± 0.01

*350 ul of peripheral blood was used as a source of DNA.

**Genomic DNA was stored at −80 °C.

***LCLs were stored at −80 °C after 2 weeks culture from EBV infection.

****Total cultivation time including 2 weeks culture before cryopreservation.

Except for the “−80 °C period” and the “Cultivation period”, the values represent the mean ± SD.