SA-magnetic bead freeze-drying working solution, SA-magnetic bead freeze-dried product and preparation method of freeze-dried product
A working solution and freeze-drying technology, which is applied to material inspection products, measuring devices, instruments, etc., can solve the problems of unstable luminescence intensity of SA-magnetic beads freeze-dried products, short storage time of SA-magnetic beads, and inconvenient transportation. Achieve the effect of being beneficial to freeze-drying, stable luminescence value, and small effect on activity
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Embodiment 1
[0033] The preparation of embodiment 1 freeze-dried working solution
[0034] Prepare the following lyophilized working solutions respectively:
[0035] Freeze-dried working solution A:
[0036] TBS buffer (10 mM Tris-HCl, 0.9% NaCl, pH: 7.4), 1% glycine, 1% inulin, 1% mannitol, 1% sodium caseinate, 0.05% Tween-20, 0.02% ProClin 300.
[0037] Freeze-dried working solution B:
[0038] TBS buffer (20 mM Tris-HCl, 0.9% NaCl, pH: 7.4), 1% glycine, 1% inulin, 2% mannitol, 2% sodium caseinate, 0.05% Tween-20, 0.02% ProClin 300.
[0039] Freeze-dried working solution C:
[0040] TBS buffer (30 mM Tris-HCl, 0.9% NaCl, pH: 7.4), 1% glycine, 2% inulin, 1% mannitol, 3% sodium caseinate, 0.05% Tween-20, 0.02% ProClin 300.
[0041] Freeze-dried working solution D:
[0042] TBS buffer (20 mM Tris-HCl, 0.9% NaCl, pH: 7.4), 1% glycine, 3% inulin, 2% mannitol, 1% sodium caseinate, 0.05% Tween-20, 0.02% ProClin 300.
[0043] Freeze-dried working solution E:
[0044] TBS buffer (40 mM Tri...
Embodiment 2
[0055] Example 2 Preparation of SA-magnetic beads freeze-dried product
[0056] 1) Adsorb SA-magnetic beads through a magnetic stand, mix SA-magnetic beads with freeze-dried working solutions A, B, C, D, E, F, G, H, I, J, and adjust the content of magnetic beads to 1 % (1 g / 100 mL).
[0057] 2) Spot SA-magnetic beads onto a 0.5cm×0.5cm glass chip with an automatic spotting instrument, 100nL per spot, 7×7 square array, 49 spots in total.
[0058] 3) Freeze-drying of SA-magnetic bead lyophilized product
[0059] Pre-freezing: the chip is put into the box at 4°C, and kept for 1 hour after entering the box, so that all samples are cooled from the same starting point of 4°C to -46°C, and kept at -46°C for 1 hour, and the samples are heated to the eutectic point The temperature was maintained for 1 hour, and then the sample was cooled again and maintained at -46°C for 2 hours.
[0060] Sublimation: Control the temperature of the plate layer to maintain the temperature of the samp...
Embodiment 3
[0064] Example 3 Redissolution and Activity Detection of SA-Magnetic Beads Freeze-dried Product
[0065] 1) Activity detection after freeze-drying and reconstitution of SA-magnetic beads
[0066] Redissolve 10 kinds of SA-magnetic bead lyophilized products with 100 μL ultrapure water;
[0067] Add 2 μL of biotinylated alkaline phosphatase (Biotin-AP) (5 ng / μL) to the 10 kinds of SA-magnetic beads after reconstitution and the same batch of non-lyophilized SA-magnetic bead suspension, and incubate at 37°C for 10 minutes.
[0068] Add 200 μL of SA-magnetic bead washing buffer, absorb and wash three times, and magnetically absorb for 3 minutes each time.
[0069] Add 200 μL enzyme substrate solution, mix well, take 170 μL to a microplate plate, incubate in a microplate reader at 37°C for 5 min, measure the luminescent signal value, and the results are shown in Table 1.
[0070] Table 1 Activity analysis of SA-magnetic beads bound to biotinylated alkaline phosphatase before and a...
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