Application of preparation for detecting serum IGF1 protein in preparation of colorectal cancer curative effect monitoring reagent
A colorectal cancer, protein technology, applied in the field of biomedicine, can solve the problems of treatment failure, side effects, low drug sensitivity, etc.
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Embodiment 1
[0016] Example 1 Differential protein screening based on DIA technology
[0017] 1. Experimental method
[0018] 1. Case information
[0019] A total of 20 patients with stage Ⅲ or stage Ⅳ colorectal cancer were included in this study, and these patients were treated with Sanjie formula and chemotherapy drugs. Quantitative proteomics technology based on full-scan data independent acquisition (DIA) of high-resolution mass spectrometry, and the changes of molecular characteristics of serum samples in 20 patients with stage III or stage IV colorectal cancer before and after treatment with Sanjie formula and chemotherapy drugs . The treatment plan of the patients is shown in Table 1.
[0020] Table 1 Diagnosis and treatment plan of 20 patients with traditional Chinese and western medicine
[0021]
[0022]
[0023] The basic process of the DIA experiment: extract protein from the sample and measure the protein concentration; digest the extracted protein sample into pepti...
Embodiment 2
[0036] PRM experimental verification
[0037] The basic process of the PRM experiment: the first step is to extract the protein from the sample and measure the protein concentration; the second step is to digest the extracted protein sample into peptides by trypsin; the third step is to pass 8 randomly selected proteins through The establishment method of DDA mode to obtain target peptide spectrum information. Fourth, take an equal amount of sample for PRM mode scanning to obtain data; fifth, use Skyline for quantitative analysis.
[0038] The detailed steps are as follows:
[0039] (1) Protein extraction: The serum samples of the above 20 patients with stage III or stage IV colorectal cancer before and after treatment with Sanjie Fang and chemotherapy drugs were randomly mixed into 5 groups, a total of 10 samples. Take 2 μL of each sample for enzyme digestion. For each sample, 1 μL of the mixed pool was used for library construction. Serum and pool samples were digested u...
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