Identification kit for circulating tumor cells of breast cancer
A breast cancer cell and tumor cell technology, applied in breast cancer circulating tumor cell identification kits, medical and biological fields, can solve the problems of contaminated blood samples, false positives, unable to detect CTCs that lose epithelial antigens, etc., to improve the accuracy and reliability, the effect of improving accuracy
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Embodiment 1
[0042] There are two types of breast cancer circulating tumor cell identification kits described in this example, with labeled probes and without labeled probes.
[0043] Wherein, breast cancer circulating tumor cell identification kit A with labeled probe mainly includes:
[0044] 1. Capture probe
[0045] The capture probe consists of three parts, from the 5' end to the 3' sequence is the sequence P1 that is complementary to the mRNA of the corresponding marker gene, the spacer sequence, and the P2 sequence that is complementary to the corresponding amplification probe P3 sequence, the same category The P2 sequences in the capture probes of the marker genes are the same. The spacer is used to space the capture probe P2 sequence from the target mRNA, and by setting a spacer sequence of appropriate length inside the probe, it can reduce steric hindrance, improve the efficiency of the hybridization reaction and the specificity of the hybridization reaction . The spacer arm o...
Embodiment 2
[0073] Example 2 Using kit A in Example 1 to detect circulating tumor cells in peripheral blood of breast cancer patients
[0074] The formula of described various solutions is as follows:
[0075]
[0076]
[0077] The probe mixture, amplification mixture, and chromogenic mixture in this example all use all the probes in the corresponding gene list of the Breast Cancer Circulating Tumor Cell Identification Kit A with Labeled Probes in Example 1.
[0078] 1. Sample pretreatment, filtering breast cancer CTCs onto the filter membrane
[0079] 1. Preserve the blood sample in the sample preservation tube with preservation solution, centrifuge at 600×g for 5 minutes, discard the supernatant, and remove the red blood cells.
[0080] 2. Add 4ml of PBS and 1ml of fixative, vortex to mix, and let stand at room temperature for 8min.
[0081] 3. Sample filtration: transfer the liquid in the sample storage tube to the filter, turn on the vacuum filtration pump to pump out the liqu...
Embodiment 3
[0141] Example 3 Using the kit A in Example 1 to detect breast cancer cell lines
[0142] 1. Selection of cell lines
[0143] The breast cancer cell marker gene of the kit of the present invention is selected from: two or more of HER2, SCGB2, MUC1, MGB1; the epithelial cell marker gene is selected from: one or more of EpCAM, CDH1, KRT7, KRT8, KRT18, KRT19 More than one; Mesenchymal cell marker gene selected from one or more of FN1, CDH2, VIMENTIN, FOXC1, TWIST1; Leukocyte marker gene is CD45. The various marker genes in the breast cancer cell marker gene, epithelial cell marker gene, mesenchymal cell marker gene and leukocyte marker gene selected in the present invention are the specific genes on breast cancer CTCs obtained by the inventor through a large number of experiments and statistical analysis. The expressed gene has good specificity and accuracy for the detection of breast cancer cells.
[0144] In this example, the epithelial-mesenchymal mixed breast cancer cell li...
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