Meningococcus capsular polysaccharide monoclonal antibodies and use thereof
A monoclonal antibody and meningococcal technology, applied in the direction of anti-bacterial immunoglobulin, instruments, biochemical equipment and methods, etc., can solve the problem of ELISA kits for rapid and effective specific detection of meningococcal capsular polysaccharides, etc. question
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Embodiment 1
[0045] Embodiment 1, establishment of hybridoma cell line
[0046] 1. Experimental materials
[0047] 1. Immunogen: The capsular polysaccharides of meningococci of groups A, C, Y, and W135 were used as immunogens (purchased from Tianjin CanSino Biotechnology Co., Ltd.).
[0048] 2. Culture medium: DMEM medium was purchased from Hyclone Company; HAT, HT selection medium and pristane were purchased from Sigma Company.
[0049] 3. Experimental animals: Balb / c mice, 8-12 weeks old, female, SPF grade animal culture.
[0050] 4. Other materials: Freund's complete adjuvant and Freund's incomplete adjuvant were purchased from Sigma Company; PEG4000 was purchased from Fluka Company; HRP-goat anti-mouse IgG antibody was purchased from JacksonImmune Company; other reagents were domestic analytically pure products.
[0051] 2. Establishment of hybridoma cell lines
[0052] 1. Animal immunity
[0053] 1) Basic immunization: The immunogen was mixed with Freund's complete adjuvant in equ...
Embodiment 2
[0065] Example 2 Preparation of Monoclonal Antibody Against ACYW135 Group Meningococcal Capsular Polysaccharide and Carrier Protein
[0066] Primary antibody preparation
[0067] The following antibody preparations were performed against hybridoma cells that can secrete monoclonal antibodies against A, C, Y, and W135.
[0068] Adult BALB / c mice were selected, and pristane was inoculated intraperitoneally, 0.5ml per mouse. After 7-10 days, the 16th generation hybridoma cells (hybridoma cells capable of secreting monoclonal antibodies against A, C, Y, and W135 were inoculated respectively) were inoculated intraperitoneally, 1×10 per mouse 6 -2×10 6 indivual. After an interval of 5 days, when the abdomen is obviously enlarged and the skin feels tense when touched with hands, the ascites can be collected with a No. 9 needle.
[0069] Centrifuge the ascitic fluid (13000r / min for 30 minutes), remove cell components and other precipitates, and collect the supernatant. Purify wit...
Embodiment 3
[0086] Example 3 Preparation of ACYW135 Group Meningococcal Capsular Polysaccharide Detection Reagent Using Purified Antibody
[0087] 1. Monoclonal antibodies Clone6B7 and Clone 6B12 for meningococcal A polysaccharide recognition by meningococcal A polysaccharide ELISA double antibody sandwich method.
[0088] Using clone 6B7 and Clone6B12 antibodies for pairing experiments, it was determined that clone 6B12 was used as the coating antibody, and HRP-labeled Clone 6B7 was used as the detection antibody. The ELISA detection method was determined, and the detection sensitivity of the kit could reach 0.008ng / mL ( image 3 ). Antibodies were labeled with the modified sodium periodate method.
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