Method for detecting ancient wool fabrics by aid of fluoroimmunoassay
A technology of immunofluorescence and detection method, which is applied in the detection field of ancient wool fabrics by immunofluorescence, can solve the problems such as the inapplicability of woolen fabrics cultural relics, and achieves the effects of high sensitivity, simple operation and avoiding interference.
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Embodiment 1
[0020] A detection method utilizing immunofluorescence to measure ancient woolen fabrics, adopts the following steps:
[0021] Raw material preparation:
[0022] PBS buffer solution of pH7.4: Weigh KCl0.2g, KH 2 PO 4 0.27g, NaCl8.0g, Na 2 HPO 4 1.42g, dissolved in 800mL distilled water and adjusted to 1000mL, adjusted to pH 7.4.
[0023] Buffered glycerol: weigh Na 2 CO 3 0.15g, NaHCO 3 0.29g, dissolved in 800mL of distilled water and adjusted to 1000mL, adjusted to pH 9.6; PBS buffer with pH 9.6 and glycerol were mixed at a volume ratio of 1:1.
[0024] Rabbit anti-wool keratin antibody diluent: Dilute the rabbit anti-wool keratin antibody with an initial concentration of 1 mg / mL by 100 times with bovine serum albumin solution with a mass concentration of 1%.
[0025] Green fluorescein-labeled goat anti-rabbit IgG (H+L) antibody diluent: Add 0.15 mg of green fluorescent microspheres and 2.7 μL of 1- (3-Dimethylaminopropyl)-3-ethylcarbodiimide solution and 10 μL of go...
Embodiment 2
[0031] A detection method utilizing immunofluorescence to measure ancient woolen fabrics, adopts the following steps:
[0032] Raw material preparation:
[0033] PBS buffer solution of pH7.4: Weigh KCl0.2g, KH 2 PO 4 0.27g, NaCl8.0g, Na 2 HPO 4 1.42g, dissolved in 800mL distilled water and adjusted to 1000mL, adjusted to pH 7.4.
[0034]Buffered glycerol: weigh Na 2 CO 3 0.15g, NaHCO 3 0.29g, dissolved in 800mL of distilled water and adjusted to 1000mL, adjusted to pH 9.6; PBS buffer with pH 9.6 and glycerol were mixed at a volume ratio of 1:1.
[0035] Rabbit anti-wool keratin antibody diluent: Dilute the rabbit anti-wool keratin antibody with an initial concentration of 1 mg / mL 10 times with bovine serum albumin solution with a mass concentration of 1%.
[0036] Green fluorescein-labeled goat anti-rabbit IgG (H+L) antibody diluent: Add 0.14 mg of green fluorescent microspheres and 2.6 μL of 1 -(3-Dimethylaminopropyl)-3-ethylcarbodiimide solution and 8 μL of goat ant...
Embodiment 3
[0042] A detection method utilizing immunofluorescence to measure ancient woolen fabrics, adopts the following steps:
[0043] Raw material preparation:
[0044] PBS buffer solution of pH7.4: Weigh KCl0.2g, KH 2 PO 4 0.27g, NaCl8.0g, Na 2 HPO 4 1.42g, dissolved in 800mL distilled water and adjusted to 1000mL, adjusted to pH 7.4.
[0045] Buffered glycerol: weigh Na 2 CO 3 0.15g, NaHCO 3 0.29g, dissolved in 800mL of distilled water and adjusted to 1000mL, adjusted to pH 9.6; PBS buffer with pH 9.6 and glycerol were mixed at a volume ratio of 1:1.
[0046] Rabbit anti-wool keratin antibody diluent: Dilute the rabbit anti-wool keratin antibody with an initial concentration of 1 mg / mL by 200 times with bovine serum albumin solution with a mass concentration of 1%.
[0047] Green fluorescein-labeled goat anti-rabbit IgG (H+L) antibody diluent: Add 0.16 mg of green fluorescent microspheres and 2.8 μL of 1 -(3-Dimethylaminopropyl)-3-ethylcarbodiimide solution and 12 μL of go...
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