Kit for pathologic diagnosis of tumors and method for staining tissue sections
A technology for pathological diagnosis and tissue sectioning, applied in the field of molecular biology, can solve the problems of high price, inactivation and high cost, and achieve the effects of less workload, rapid detection and easy operation.
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[0041] This embodiment also provides a method for preparing a probe for tumor pathological diagnosis, including the following steps:
[0042] 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.
[0043] 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.
[0044] 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.
[0045] In this embodiment, the ...
Embodiment 1
[0065] The antibody is an anti-HER2 protein antibody, and the paraffin tumor tissue section is human breast cancer cell MCF7
[0066] 1. Preparation of probes for pathological diagnosis of tumors
[0067] 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.
[0068] 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.
[0069] 3. Alkynyl modification of anti-HER2 protein antibody: Add DBCO-sulfo-NHS Ester alkynylation reagent to anti-HER2 protein antibody and re...
Embodiment 2
[0094] The antibody is an anti-HER2 protein antibody, and the paraffin tumor tissue section is human liver cancer cell HepG2.
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