Antibody for inhibitting growth of colorectal carcinoma and its use in preparation of medicament and kit
An antibody and antibody light chain technology, applied in biochemical equipment and methods, applications, antibodies, etc., can solve the problems of low specificity, specificity and sensitivity that cannot meet clinical needs, etc.
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Embodiment 1 3
[0045] Example 1. Establishment of 3P9 Monoclonal Antibody Hybridoma Cell Line and Production of Monoclonal Antibody
[0046] Materials: 1. Cells SW1116 colon cancer cell line, purchased from ATCC (American TypeCulture Collection, ATCC No. CCL-233), SP2 / 0 mouse myeloma cells (ATCC No. CRL-1581). 2. Medium Serum-free DMEM, high-glucose DMEM, HAT, and HT medium were purchased from Gibco, fetal bovine serum was purchased from Wuhan Sanli Company, and cell culture plates were Corning products. 3. Reagent polyethylene glycol PEG (MW 4000) Purchased from Sigma Company, other reagents were domestic analytical grade 4. Animals BALB / c mice were purchased from Institute of Experimental Animals, Chinese Academy of Medical Sciences. 5. Antibody identification The mouse monoclonal antibody typing reagent Sigma ImmunoType Kit antibody subtype detection kit was used.
[0047] Method: 1. Mice were immunized with 1×10 7 Mix and emulsify SW1116 cell suspension with 0.5ml of Freund's complet...
Embodiment 2 3P9
[0054] Example 2. Purification and biochemical properties of 3P9 monoclonal antibody
[0055] Materials: 3P9 monoclonal antibody ascites was obtained by inoculating BALB / c mice with hybridoma cells intraperitoneally; prepacked chromatography column Sephadex-200, column volume 100ml, Phamacia product, horseradish peroxidase (HRP) goat anti-mouse The IgM antibody was purchased from Sant Cruz Company, and the ECL fluorescence detection kit was purchased from Pierce Company, and was purified using the AKTA FPLC protein chromatography system.
[0056] Method: Thaw the above ascites at 4°C, centrifuge at 15,000g for 20 minutes, collect the supernatant, and sterilize with a 0.2um membrane; equilibrate the prepacked column with 0.01M PBS at pH 7.2, load 5ml of ascites; wash with 0.01M PBS at pH 7.2 The flow rate was 1ml / min, and each elution peak was collected; 10ul samples of the elution peak were spotted on a nitrocellulose membrane, and after natural air drying, dot hybridization...
Embodiment 3 3P9
[0059] Example 3. Binding of 3P9 monoclonal antibody to bovine submandibular gland mucin
[0060] Materials: 3P9 monoclonal antibody was purified from ascites antibody by Sephadex-200; purified bovine submaxillary mucin (BSM, bovine submaxillary mucin) (Sigma), horseradish peroxidase (HRP) goat anti-mouse IgM antibody was purchased from Sant Cruz Company; 96-well enzyme-linked immunosorbent assay plate was purchased from Corning Costar, USA.
[0061] Method: Dilute BSM to 50ng / ml in the coating solution, add 100ul to each plate well, room temperature for 2 hours or overnight at 4°C, shake off the coating solution, wash with PBS, block with 2% BSA-PBS for 1 hour, add 50ul for serial dilution and purification The 3P9 monoclonal antibody was incubated at 37°C for 1 hour, washed with PBS or PBST, added 50ul horseradish peroxidase (HRP) goat anti-mouse IgM antibody (diluted 2,000 times in PBS) and incubated at 37°C for 1 hour, washed with PBS or PBST Wash, add 200ul color develo...
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