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. 2007 Oct 31;56(1):49–56. doi: 10.1007/s10616-007-9106-z

Fig. 4.

Fig. 4

Analysis of genomic DNA from different cell lines using actin primer pairs detecting both, Chinese and Syrian (Golden) hamster cell lines. Primer: (a) act-bHam-1F and act-bHam-1R; (b) primer: act-bHam-2F and act-bHam-2R. Amplified DNA fragments were detected after ethidium bromide staining of 1.2% agarose gels. Lane 1, 1G1 (ACC 424); lane 2, 2E10H2 (ACC 178); lane 3, A-10 (ACC 132); lane 4, A-S-30D (ACC 208); lane 5, B-16V (ACC 370); lane 6, CHO-DHFR (ACC 126); lane 7, C6-BU-1 (ACC 108); lane 8, GH3 (ACC 464); lane 9, HPD-1NR (ACC 314); lane 10, HPD-2NR (ACC 293); lane 11, MMQ (ACC 484); lane 12, MS-5 (ACC 441); lane 13, HELA (ACC 57); lane 14, COS-1 (ACC 63); lane 15, V-79 (ACC 335); lane 16, HL-60 (ACC 3); lane 17, water control (no DNA). H, Hamster; M, Mouse; P, Primate; R, Rat; W, Water control (no DNA). The arrows indicate the DNA molecular weight markers of 500, 900 and 1,000 bp