Fig. 3.
Fig. 3. Demonstration of clonotypic PCR before and after treatment in an nPR patient. / (A) Clonotypic PCR product in the initial pretreatment samples of this patient at a 10−4 dilution in the BM after primary PCR. (B) After seminested PCR, the clonotype is detected at a 10−4 dilution with greater intensity confirming the previous primary PCR result. (C) Persistent clonotype PCR after treatment from a nodular PR BM specimen for this same patient. Primary PCR detects a clone at a 10−2 dilution. (D) Seminested PCR confirms the primary PCR finding, detecting a clone at a 10−2 dilution. DNA was extracted from an aspirate corresponding to the bone marrow biopsy shown in Figure 4B. (A-D) Lanes 1-8, serial 10-fold dilutions of patient DNA starting with a 100 ng template; lane 9, negative control with no template DNA; lane 10, 1 ug polyclonal DNA; lane 11, positive control with bcl-2 primers and 100 ng of template.

Demonstration of clonotypic PCR before and after treatment in an nPR patient.

(A) Clonotypic PCR product in the initial pretreatment samples of this patient at a 10−4 dilution in the BM after primary PCR. (B) After seminested PCR, the clonotype is detected at a 10−4 dilution with greater intensity confirming the previous primary PCR result. (C) Persistent clonotype PCR after treatment from a nodular PR BM specimen for this same patient. Primary PCR detects a clone at a 10−2 dilution. (D) Seminested PCR confirms the primary PCR finding, detecting a clone at a 10−2 dilution. DNA was extracted from an aspirate corresponding to the bone marrow biopsy shown in Figure 4B. (A-D) Lanes 1-8, serial 10-fold dilutions of patient DNA starting with a 100 ng template; lane 9, negative control with no template DNA; lane 10, 1 ug polyclonal DNA; lane 11, positive control with bcl-2 primers and 100 ng of template.

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