• No results found

Quantitative detection of DNMT3A R882H mutation in acute myeloid leukemia

N/A
N/A
Protected

Academic year: 2020

Share "Quantitative detection of DNMT3A R882H mutation in acute myeloid leukemia"

Copied!
11
0
0

Loading.... (view fulltext now)

Full text

Loading

Figure

Fig. 1 Assay design of ASB-PCR. Primers and probe are located in exon 23 of DNMT3A. The allele-specific primer contains the mutational spot atits 3′-end whereas the wt spot is incorporated in the middle of the blocker (red box)
Table 1 Oligonucleotides used in this study
Fig. 3 Analysis of PCR sensitivity using serial dilutions of DNA (a) and (b) dilution of mutated DNA with wt DNA
Fig. 4 Sequence of R882H plasmid. a Heterozygote R882H mutation in a patient sample. The mutational spot is indicated by the red box
+5

References

Related documents

Outdoor studies including all its sub-sets, seems to be more developed and accepted in pre-school and early years education through outdoor play, easier to implement in

Greer and colleagues 16 using the Hos- pital Anxiety and Depression Scale as a brief screening tool in a cohort of recently diagnosed cancer patients, detected a 22% combined rate

However, there is substantial further skill requirement in both wind and solar manufacturing and services, especially in the south of Egypt (Upper Egypt) where the climatic

Use the following scenario and questions for a class discussion. Use the possible answers to guide the students and the Discussion Rubric for assessment. Scenario: Imagine yourself

The study was aimed: to determine the social demographic profile of severely malnourished children and/or parents of children with severe acute malnutrition, to

Results: The RBCp experienced efficient tumor targeting and long tumor retention for almost 4 h after intravenous injection, and the superior signal-to-noise ratio at the optimal

Similarly to Figure 6.a, which shows that 1- min changes in Sym/H are very strongly correlated with speed jump, the outliers have a slight linear correlation with speed

concentration such that 50% of all noninstitutionalized civilian women ages 16 to 49 years during the survey period have total serum PBDE concentrations below this level;