Method for detecting collagen in ancient cultural relic material
A technology of collagen and ancient cultural relics, which is applied in the detection field of collagen in ancient cultural relic materials, can solve the problems of inability to carry out efficient identification, and achieve the effects of low cost, simple detection and fast response
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Embodiment 1
[0024] a) Solution preparation: preparation of PBS buffer solution: KCl 0.2g, KH 2 PO 4 0.2g, NaCl 8.0g, NaH 2 PO 4 ·7H 2 O 2.16g, dissolved in deionized water and made to a volume of 1000mL, adjusted to pH 7.4, sterilized at 121°C. Preparation of eluent: 5mL1mol / L trishydroxymethylaminomethane-HCl buffer solution, 1mL0.5mol / L ethylenediaminetetraacetic acid solution, 180g urea, 25mL20% sodium lauryl sulfate (50mL deionized water containing 10 g of solute), dissolved in deionized water and adjusted to 500 mL, adjusted to pH 7.4 with NaOH, and stored at room temperature after sterile suction filtration.
[0025] b) 100 μL of PBS buffer solution was set as a blank control, and 0.1 mg of fish gelatin powder was set as a positive control. Dissolve 100 μL of PBS buffer solution of blank sample, 0.1 mg of fish gelatin powder of positive control sample and 0.1 mg of cultural relic material of experimental sample in 100 μL of eluent respectively, and place it at room temperature...
Embodiment 2
[0041] A method for detecting collagen in ancient cultural relic materials, it comprises the steps:
[0042] a) Solution preparation: preparation of PBS buffer solution: KCl 0.2g, KH 2 PO 4 0.2g, NaCl 8.0g, NaH 2 PO 4 ·7H 2 O 2.16g, dissolved in deionized water and made to a volume of 1000mL, adjusted to pH 7.4, sterilized at 121°C. Preparation of eluent: 5mL1mol / L trishydroxymethylaminomethane-HCl buffer solution, 1mL0.5mol / L ethylenediaminetetraacetic acid solution, 180g urea, 25mL20% sodium lauryl sulfate (50mL deionized water containing 10 g of solute), dissolved in deionized water and adjusted to 500 mL, adjusted to pH 7.4 with NaOH, and stored at room temperature after sterile suction filtration.
[0043] b) 100 μL of PBS buffer solution was set as a blank control, and 0.1 mg of fish gelatin powder was set as a positive control. Dissolve 100 μL of blank sample PBS buffer solution, 0.1 mg of positive control sample fish gelatin powder and 0.3 mg of experimental sam...
Embodiment 3
[0059] A method for detecting collagen in ancient cultural relic materials, it comprises the steps:
[0060] a) Solution preparation: preparation of PBS buffer solution: KCl 0.2g, KH 2 PO 4 0.2g, NaCl 8.0g, NaH 2 PO 4 ·7H 2 O 2.16g, dissolved in deionized water and made to a volume of 1000mL, adjusted to pH 7.4, sterilized at 121°C. Preparation of eluent: 5mL1mol / L trishydroxymethylaminomethane-HCl buffer solution, 1mL0.5mol / L ethylenediaminetetraacetic acid solution, 180g urea, 25mL20% sodium lauryl sulfate (50mL deionized water containing 10 g of solute), dissolved in deionized water and adjusted to 500 mL, adjusted to pH 7.4 with NaOH, and stored at room temperature after sterile suction filtration.
[0061] b) 100 μL of PBS buffer solution was set as a blank control, and 0.1 mg of fish gelatin powder was set as a positive control. Dissolve 100 μL of PBS solution of blank sample, 0.1 mg of fish gelatin powder of positive control sample, and 0.5 mg of cultural relic m...
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