Detection marker for diabetic nephropathy
A technology of diabetic nephropathy and markers, applied in the field of diabetic nephropathy detection markers, can solve problems such as difficult early detection of diabetic nephropathy, and achieve the effects of convenient collection, good specificity, and improved specificity and accuracy
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Embodiment 1
[0029] Diabetic nephropathy detection marker of the present invention is:
[0030] Keratin 19, haptoglobin, apolipoprotein E, C-reactive protein, platelet factor 4 precursor, sex hormone-binding globulin precursor, immunoglobulin heavy chain Viiiregionhil, complement component C4, keratin 6l, C-reactive protein precursor Splice isoform 1, serine / threonine protein kinase WNK4 and CD 5 antigen.
Embodiment 2
[0032] In this application, 12 kinds of proteins in serum or urine (ie, keratin 19, haptoglobin, apolipoprotein E, C-reactive protein, platelet factor 4 precursor, sex hormone-binding globulin precursor, Immunoglobulin heavy chain Viiiregionhil, complement component C4, keratin 6l, C-reactive protein precursor splice isoform 1, serine / threonine protein kinase WNK4 and CD 5 antigen), and then buckle the differential spots on the two-dimensional electrophoresis gel Points, do mass spectrometry, determine the name of the protein and its size, and compare and analyze the protein content in the serum or urine of the healthy control group and diabetic nephropathy patients. The specific operation is as follows:
[0033] 1. The detection substance is serum
[0034] 1. Prepare healthy control serum: The healthy control serum is collected from healthy people, and the expression levels of the above 12 proteins in the serum are within the normal range.
[0035] The healthy control serum...
Embodiment 3
[0137] Diabetic nephropathy detection kit of the present invention:
[0138] 1. Collect serum from 2-3 healthy people, and the expression levels of the above 12 proteins in the serum are within the normal range. Freeze at -80°C after collection. as a standard negative serum;
[0139] 2. Prepare the solution used for electrophoresis (if there is any improvement, just write it here, corresponding to Example 2);
[0140] 3. Prepare the standard plate: put figure 1 with Image 6 Printed, as a standard plate. After the detection, it can be judged according to the electrophoresis results of the standard plate or the standard negative serum.
[0141] The detection method of the detection kit of the present invention is carried out according to Example 2 (the step of performing mass spectrometry analysis on the difference points is omitted).
[0142] The test results are judged based on: when keratin 19, haptoglobin, apolipoprotein E, C-reactive protein, platelet factor 4 precur...
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