A gene diagnostic kit for diagnosing and predicting bone metastasis of luminal B breast cancer
A gene diagnosis and kit technology, applied in the field of biochemistry, can solve problems such as increasing the burden on patients, high examination costs, and increasing pressure
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0077] Example 1: Bone Metastasis of Luminal A Breast Cancer
[0078] 1. Experimental samples and experimental methods
[0079] 1. Experimental samples
[0080] The test set and validation set of the non-metastasis group of breast cancer in LuminalA type and the bone metastasis group of breast cancer in LuminalA type.
[0081] 2. Total DNA extraction from serum
[0082] Serum DNA was extracted according to the instructions of the DNABlood Midi Kit, and 0.8 mL of serum was used for each sample. The purity of the extracted DNA was detected by an ultraviolet spectrophotometer, and the absorbance A260 / A280 ratio was between 1.7-2.0 for subsequent operations. Calculate the DNA content and store at -70°C for later use.
[0083] 3. DNA sulfite modification and pyrosequencing detection
[0084] DNA sulfite modification:
[0085] Take 1 μg of DNA, perform methylation modification on genomic DNA according to the instructions of DNAMethylation-Goldkit, and store it at -70°C for futur...
Embodiment 2
[0124] Example 2: Bone metastasis of Luminal B breast cancer
[0125] 1. Experimental samples and experimental methods
[0126] 1. Experimental samples
[0127] The test set and validation set of the breast cancer non-metastasis group in Luminal B type and the bone metastasis group of Luminal B breast cancer group.
[0128] 2. Total DNA extraction from serum
[0129] Serum DNA was extracted according to the instructions of the DNABlood Midi Kit, and 0.8 mL of serum was used for each sample. The purity of the extracted DNA was detected by an ultraviolet spectrophotometer, and the absorbance A260 / A280 ratio was between 1.7-2.0 for subsequent operations. Calculate the DNA content and store at -70°C for later use.
[0130] 3. DNA sulfite modification and pyrosequencing detection
[0131] DNA sulfite modification:
[0132] Take 1 μg of DNA, perform methylation modification on genomic DNA according to the instructions of DNA Methylation-Gol dkit, and store it at -70°C for future...
Embodiment 3
[0171] Example 3: Her-2 overexpression breast cancer bone metastasis
[0172] 1. Experimental samples and experimental methods
[0173] 1. Experimental samples
[0174] The test set and validation set of the Her-2 overexpression breast cancer non-metastasis group and the Her-2 overexpression breast cancer bone metastasis group.
[0175] 2. Total DNA extraction from serum
[0176] Serum DNA was extracted according to the instructions of the DNA Blood Midi Kit, and 0.8 mL of serum was used for each sample. The purity of the extracted DNA was detected by an ultraviolet spectrophotometer, and the absorbance A260 / A280 ratio was between 1.7-2.0 for subsequent operations. Calculate the DNA content and store at -70°C for later use.
[0177] 3. DNA sulfite modification and pyrosequencing detection
[0178] DNA sulfite modification:
[0179]Take 1 μg of DNA, perform methylation modification on genomic DNA according to the instructions of DNAMethylation-Goldkit, and store it at -70...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


