Hybridoma cell line, cd68 monoclonal antibody, preparation method and application
A hybridoma cell line and monoclonal antibody technology, applied in the field of biomedicine, can solve the problems of high preparation cost and poor stability of monoclonal antibodies, and achieve the effects of high specificity and sensitivity, and improved accuracy
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Embodiment 1
[0038] Example 1 Preparation of CD68 Monoclonal Antibody
[0039] 1) Immunogen preparation
[0040] Using eukaryotically expressed CD68 protein as the immunogen, the eukaryotically expressed CD68 protein is CD68 protein expressed by human engineered cells (purchased from Beijing Shenzhou Yiqiao, article number: 11192-H08B1), immunized female Balb / c mice, and obtained spleen lymph Cells were used for hybridoma fusion experiments.
[0041] 2) Immunization of Balb / c mice with immunogen
[0042] The purified recombinant CD68 protein was dissolved and diluted to 1.0 mg / mL with 10 mmol / LPBS of pH 7.4 after measuring the protein content. Seven female Balb / c mice aged 6-8 weeks and with equal body weight were selected. For the first immunization, CD68 protein was emulsified and mixed with an equal volume of Freund's complete adjuvant as the immunogen; the second and third immunizations were performed every two weeks, and the adjuvant was changed to Freund's incomplete adjuvant; 3 d...
Embodiment 2
[0069] Example 2 Screening of the best CD68 monoclonal antibody combined with CD68 antigen
[0070] The technical scheme of immunohistochemistry (enzyme-labeled antibody indirect method), the obtained group of CD68 antibodies is used to immunohistochemically stain the serial sections of the same tissue under the same conditions, and the antibody with the strongest specificity and highest titer is screened out of the antibodies , and detect the expression of the CD68 monoclonal antibody of the present invention on the tumor tissue.
[0071] 1) Paraffin sections of giant cell tumor tissue were routinely dewaxed and hydrated: the sections were baked at 65°C for 30 minutes, soaked in xylene for 15 minutes×2 times; soaked in absolute ethanol for 10 minutes×2 times; Soak in % alcohol, 85% alcohol, 75% alcohol for 5 minutes each; soak in distilled water for 5 minutes x 3 times;
[0072] 2) Antigen retrieval:
[0073] Add 500mL citric acid repair solution (pH6.0) into the stainless ...
Embodiment 3
[0089] Example 3 Comparing CD68 Monoclonal Antibody Immunohistochemical Detection Specificity
[0090] Choose to purchase CD68 monoclonal antibody from Beijing Zhongshan in China, use the manual and explore the best conditions for 17E11, stain the same tumor tissue sections respectively, compare the staining conditions, and determine whether the specificity is consistent. The specific operation is as follows:
[0091] 1) Paraffin tissue sections of giant cell tumor of bone, colorectal cancer, and lung cancer tissue were routinely dewaxed and hydrated: the sections were baked in an incubator at 65°C for 30 minutes, soaked in xylene for 15 minutes, twice; Soak in absolute ethanol for 10 minutes, twice; soak in 95% alcohol, 85% alcohol, and 75% alcohol for 5 minutes each; soak in distilled water for 5 minutes x 3 times;
[0092] 2) Antigen restoration: 0.01M citric acid restoration solution (pH6.0), high-pressure restoration for 2min30s; soaking in distilled water for 5min×3 time...
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