CD74-ROS1 rearrangement DNA (deoxyribonucleic acid) standard substance for molecular diagnosis, RNA (ribonucleic acid) standard substance for molecular diagnosis and application of CD74-ROS1 rearrangement DNA standard substance and RNA standard substance
A technology of molecular diagnosis and standard products, which is applied in the direction of DNA/RNA fragments, recombinant DNA technology, microbial measurement/inspection, etc., can solve the problems of low success rate, small amount, non-reproducible samples, etc., and achieve complete and accurate breakpoints Effect
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[0040] The present invention also provides a method for preparing cells for DNA standard or RNA standard, comprising the steps of:
[0041] (1) Construct the sgRNA targeting intron 6 of the CD74 gene on the vector pX330 to obtain plasmid C4;
[0042] (2) Construct the sgRNA targeting intron 33 of the ROS1 gene on the vector pX330 to obtain plasmid R3;
[0043] (3) Co-transfect the host cells with plasmid C4 and plasmid R3 to obtain recombinant cells;
[0044] (4) Perform monoclonalization of recombinant cells to obtain cells for preparing DNA standards or RNA standards.
[0045] In the present invention, the sequence of the sgRNA targeting intron 6 of the CD74 gene in step (1) is preferably as shown in SEQ ID NO.18.
[0046] In the present invention, the sequence of the sgRNA targeting intron 33 of the ROS1 gene in step (2) is preferably as shown in SEQ ID NO.27.
[0047] In the present invention, the monoclonalization in step (4) is preferably carried out by the limiting d...
experiment example 1
[0056] Select mother cells with higher plasmid transfection efficiency as alternative infected host cells, as shown in Table 2:
[0057] Table 2 Sources and media of different host cell lines
[0058] cell line source culture medium HEK293 ATCC;CRL-1573 DMEM+10%FBS HCT116 ATCC;CCL-247 McCoy's 5a+10%FBS DLD-1 ATCC;CRL-2577 RPMI-1640+10%FBS RKO ATCC;CCL-221 MEM+10%FBS SW48 ATCC;CCL-231 DMEM+10%FBS
[0059] According to the instructions published by ATCC, culture 5 cell lines, adjust to the exponential growth phase, plate the cells into 6-well plates at a density of 1x10e6cell / well, and culture overnight;
[0060] The next day, the cells were observed under a microscope. When the confluence of the cells reached 80%, the plasmid PX458 with GFP was transfected into 5 kinds of host cells, 1.5 μg / well, and the transfection method followed the instructions of lipo3000. The expression of GFP in the cells was observed with ...
experiment example 2
[0093] ddPCR detects the copy number of CD74-ROS1 rearrangement standard cells at the DNA level:
[0094] Clone No. 23 with CD74-ROS1 rearrangement was selected, and ddPCR was designed to detect the frequency of the rearrangement of interest, and the target sequence was shown in SEQID NO.35.
[0095] Design ddPCR for the sequence of interest:
[0096] CD74-ROS1-23-F is shown in SEQ ID NO.36;
[0097] CD74-ROS1-23-R is shown in SEQ ID NO.37;
[0098] CD74-ROS1-23-P is shown in SEQ ID NO.38;
[0099] ROS1-T-23-F is shown in SEQ ID NO.39;
[0100] ROS1-T-23-R is shown in SEQ ID NO.40;
[0101] ROS1-T-23-P is shown in SEQ ID NO.41.
[0102] The ddPCR test showed that the rearrangement frequency of CD74-ROS1 in clone 23 was 50%, that is, there were 2 copies of ROS1 in HCT116, 1 copy was rearranged, and the other 1 copy did not occur. Such as Figure 4 shown. The FAM probe detects the copy number of CD74-ROS1 rearrangement, and the VIC probe detects the overall copy number o...
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