Use of lncrna composition and preparation diagnosis predicting luminal type A breast cancer bone metastases gene diagnostic kit
A technology for gene diagnosis and breast cancer, applied in the field of biochemistry, can solve the problems of increasing patient burden, high inspection costs, and increasing pressure
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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 the total RNA were measured at 260nm with a NanoDropND-2000 spectrophotometer (Thermo Scientific). The electrophoresis test showed that the purified RNA was of good quality before subsequent operations. 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 c...
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 the total RNA were measured at 260nm with a NanoDropND-2000 spectrophotometer (Thermo Scientific). The electrophoresis test showed that the purified RNA was of good quality before subsequent operations. 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 collect...
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 the total RNA were measured at 260nm with a NanoDropND-2000 spectrophotometer (Thermo Scientific). The electrophoresis test showed that the purified RNA was of good quality before subsequent operations. 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...
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