Probe for pathological diagnosis of tumor, and preparation method and application thereof
A pathological diagnosis and tumor technology, applied in the field of molecular biology, can solve the problems of peroxidase variability, inconvenient storage and use, and false negative test results.
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[0039] This embodiment also provides a method for preparing a probe for tumor pathological diagnosis, such as figure 1 shown, including the following steps:
[0040] Step S110, mixing the chloroauric acid solution with a concentration of 1-100 mmol / L and the bovine serum albumin or human serum albumin solution with a concentration of 1-500 mg / mL evenly, and then adding a NaOH solution with a concentration of 0.1-10 mol / L , and incubated in a shaker at 0-100° C. for 3-100 hours to obtain gold nanoclusters, wherein the molar ratio of NaOH to chloroauric acid is 1:1-1:100.
[0041] In this embodiment, bovine serum albumin is preferred to prepare gold nanoclusters, because bovine serum albumin has the advantages of non-toxicity, good biocompatibility, and relatively cheap price.
[0042] Step S120 , mixing the gold nanoclusters with the azide reagent pretreated by NHS at a molar ratio of 1:1 to 1:100 to obtain gold nanoclusters with azide groups modified on the surface.
[0043]...
Embodiment 1
[0064] The antibody is an anti-HER2 protein antibody, and the paraffin tumor tissue section is human breast cancer cell MCF7
[0065] 1. Preparation of gold nanocluster probes
[0066] 1. Preparation of gold nanoclusters: at 37°C, add 0.5mL of chloroauric acid solution with a concentration of 50mmol / L to 0.5mL of BSA solution with a concentration of 200mg / mL and mix well; then add 0.2mL with a concentration of 1mol / L of NaOH solution to obtain a mixed solution; the mixed solution was placed in a shaker and incubated at 37°C for 10 hours to obtain gold nanoclusters.
[0067] 2. Azido group modification of gold nanoclusters: mix the above gold nanoclusters with the azide reagent at a molar ratio of 1:1 to obtain gold nanoclusters with azide groups on the surface, wherein the azide reagent Pre-treated by the NHS.
[0068] 3. Alkynyl modification of anti-HER2 protein antibody: Add DBCO-sulfo-NHS Ester alkynylation reagent to anti-HER2 protein antibody and react for 30 minutes, ...
Embodiment 2
[0091] The antibody is an anti-HER2 protein antibody, and the paraffin tumor tissue section is human liver cancer cell HepG2.
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