Markers and methods for detection of colorectal cancer or esophageal cancer
A marker and technology for esophageal cancer, applied in biochemical equipment and methods, chemical instruments and methods, microbial measurement/testing, etc., can solve problems such as difficult to interpret results, high false positive rate, and time-consuming
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[0115] The present invention will be described more specifically below by way of examples. However, the present invention is not limited by this example.
[0116]
[0117] (1) Production of hollow fiber filter
[0118] Bundle 100 polysulfone hollow fibers with a molecular weight cut-off of about 50,000 on the membrane surface, and fix the two ends on the glass tube with an epoxy resin-based encapsulant on the premise that the hollow part of the hollow fiber is not blocked. into micromodules. This miniature module (module A) can be used to remove high molecular weight proteins in serum or plasma, with a diameter of about 7 mm and a length of about 17 cm. A micromodule (module B) for concentrating low-molecular-weight proteins was similarly fabricated using a membrane with a pore size of molecular weight cut-off about 3 k. The micromodule has an inlet connected to the hollow fiber lumen at one end and an outlet at the other end. The inlet and outlet of the hollow fiber mic...
Embodiment 2
[0128] (1) Detection of COTL1 protein in esophageal cancer blood by Western blot
[0129]Plasma samples were obtained from 3 esophageal cancer patients (No. 1-3) and 4 healthy controls (No. 1-4) who obtained informed consent. 100 μL of Affi-Gel blue glue (Bio-Rad) and 50 μL of Protein A-Sepharose (GE Healthcare) were added to 100 μL of each sample, and reacted overnight at 4°C to remove albumin and immunoglobulin in the sample. The sample thus obtained was solubilized and boiled using SDS loading buffer (50mM Tris hydrochloric acid, pH 6.8, 1mMDTT, 5% SDS, 10% glycerol), and subjected to SDS-polyacrylamide gel (16%) electrophoresis, Proteins were then transferred to PVDF membranes. This was reacted with a rabbit anti-COTL1 polyclonal antibody (Proteintech Group) and a peroxidase-labeled secondary antibody (anti-rabbit IgG antibody). Immunoreactive proteins were visualized by sensitizing the X-ray film using SuperSignalWestFemtoMaximumSensitivitySubstrate (Pierce), and the si...
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