Antibody detection kit (OmpC-IgA)
A technology for detecting kits and antibodies, which is applied in biological testing, measuring devices, material inspection products, etc., and can solve the problems of not detecting OmpC antibody ELISA kits, etc.
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Embodiment 1
[0014] Example 1 Preparation of Escherichia coli OmpC
[0015] Reagents and instruments
[0016] 1) Reagent
[0017] Escherichia coli host bacteria DH5α, BL21(DE3), cloning vector pCR2.1T-vector, expression plasmid pET28a(+), DNA polymerase rTaq, T4 DNA ligase, DNA polymerase rTaq, LATaq and restriction endonuclease BamH I, Hind III and EcoR I, BamH I, DL2000 DNA Marker, T4 DNA ligase, low molecular weight standard protein, DNA gel recovery kit, IPTG, etc.
[0018] 2) Instrument
[0019] Ordinary shaker SCS-24; water-proof constant temperature electric heating incubator; Biophotometer spectrophotometer, desktop refrigerated centrifuge Centrifuge 5810R, desktop centrifuge MiniSpin; high-speed refrigerated centrifuge; protein electrophoresis and gel imaging system; PCR instrument; ultrasound Lysis instrument; constant temperature metal bath; HIS protein purification column, etc.
[0020] 3) Experimental method
[0021] vector construction
[0022] Primers ATTG GATC CGCT CC...
Embodiment 2
[0027] Example 2 Preparation of enzyme-labeled anti-human IgA antibody
[0028] Horseradish peroxidase-labeled anti-antibody: The enzyme-labeled anti-human IgA antibody was obtained by coupling the anti-human IgA antibody with horseradish peroxidase by the glutaraldehyde method. The method is to dissolve 10mg of HRP in 0.2ml of PH6.80.mol / LPBS containing 1.25% glutaraldehyde,
[0029] Dissolve 10mg of HRP in 1ml of 0.2mol / L pH5.6 acetate buffer, dissolve and mix well, then add 1ml of 0.1mol / L NaI04 solution, mix well, put it in the refrigerator for 20min, take it out and add 0.4mol / L ethylene glycol solution 0.5ml, after standing at room temperature for 30min, add 1ml of aqueous solution (or PBS) containing 5mg of anti-human IgA antibody, mix well and put in a dialysis bag, slowly stir and dialyze with 0.05mol / L, pH value 9.6 sodium carbonate buffer for 6h (or overnight ) to combine, then take out and add 0.2ml of NaBH4 solution (5mg / ml), and put it in the refrigerator for 2h...
Embodiment 3
[0030] Example 3 microwell plate coating
[0031] Coating buffer: pH9.60.5mol / L sodium bicarbonate buffer
[0032] Blocking solution: 1% BSA (bovine serum albumin) in PBS
[0033] Dilute OmpC with coating buffer, add 100ul to each well, incubate at 37°C for 2h or overnight at 4°C; pour off the coating solution, wash with washing solution 5 times, each time for 1min; pat dry, then add to each well 200ul blocking solution, incubate at 37°C for 2h; pour off the liquid in the well, dry and store in a vacuum-sealed aluminum film.
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