Fig. 4.
Fig. 4. Amplification of genomic breakpoint on derivative chromosome 5. Genomic DNA was subjected to standard and nested amplification, followed by product separation on a 1% agarose gel. Ethidium bromide staining of standard DNA-PCR products (A) and of nested DNA-PCR products (D). Lanes 1 through 11, cases no. 1 through 11; lane 12, t(2;5)+ SU-DHL-1 cell line; lane M, molecular weight marker 1-kb DNA ladder (GIBCO-BRL). The gels were transferred to a nylon membrane and hybridized either with the ALK-5P (radioautographies B and E) or the NPM-5P (radioautographies C and F). The sizes are indicated in bases.

Amplification of genomic breakpoint on derivative chromosome 5. Genomic DNA was subjected to standard and nested amplification, followed by product separation on a 1% agarose gel. Ethidium bromide staining of standard DNA-PCR products (A) and of nested DNA-PCR products (D). Lanes 1 through 11, cases no. 1 through 11; lane 12, t(2;5)+ SU-DHL-1 cell line; lane M, molecular weight marker 1-kb DNA ladder (GIBCO-BRL). The gels were transferred to a nylon membrane and hybridized either with the ALK-5P (radioautographies B and E) or the NPM-5P (radioautographies C and F). The sizes are indicated in bases.

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