A gene diagnostic kit for diagnosing and predicting her-2 overexpression breast cancer bone metastasis
A gene diagnosis, breast cancer technology, applied in the field of biochemistry, can solve the problems of increasing pressure, increasing patient burden, and high inspection costs
- 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 Luminal A type and the bone metastasis group of breast cancer in Luminal A type.
[0081] 2. RNA extraction and qRT-PCR
[0082] Total RNA was extracted from serum samples using Trizol reagent (Invitrogen, Shanghai, China). The concentration and purity of total RNA were measured at 260nm with a NanoDropND-2000 spectrophotometer (Thermo Scientific). Electrophoresis detection showed that the purified RNA was of good quality and followed up. Total RNA was converted into cDNA using a reverse transcription kit (Takara, Dalian, China). Fluorescent quantitative PCR (Takara, Dalian, China) was carried out using the SYBR Green method, and ABI Prism7000 fluorescent quantitative PCR system (Agilent Technologies) was used for data collection. The ...
Embodiment 2
[0105] Example 2: Bone metastasis of Luminal B breast cancer
[0106] 1. Experimental samples and experimental methods
[0107] 1. Experimental samples
[0108]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.
[0109] 2. RNA extraction and qRT-PCR
[0110] Total RNA was extracted from serum samples using Trizol reagent (Invitrogen, Shanghai, China). The concentration and purity of total RNA were measured at 260nm with a NanoDropND-2000 spectrophotometer (Thermo Scientific). Electrophoresis detection showed that the purified RNA was of good quality and followed up. Total RNA was converted into cDNA using a reverse transcription kit (Takara, Dalian, China). Fluorescent quantitative PCR (Takara, Dalian, China) was carried out using the SYBR Green method, and ABI Prism7000 fluorescent quantitative PCR system (Agilent Technologies) was used for data collection. The primer...
Embodiment 3
[0133] Example 3: Her-2 overexpression breast cancer bone metastasis
[0134] 1. Experimental samples and experimental methods
[0135] 1. Experimental samples
[0136] 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.
[0137] 2. RNA extraction and qRT-PCR
[0138]Total RNA was extracted from serum samples using Trizol reagent (Invitrogen, Shanghai, China). The concentration and purity of total RNA were measured at 260nm with a NanoDropND-2000 spectrophotometer (Thermo Scientific). Electrophoresis detection showed that the purified RNA was of good quality and followed up. Total RNA was converted into cDNA using a reverse transcription kit (Takara, Dalian, China). Fluorescent quantitative PCR (Takara, Dalian, China) was carried out using the SYBR Green method, and ABI Prism7000 fluorescent quantitative PCR system (Agilent Technologies) was used for data collection...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com