Method for determining subcellular distribution of graphene in rice
A graphene and subcellular technology, applied in the direction of measuring devices, analytical materials, color/spectral characteristic measurement, etc., to achieve the effect of easy operation and simple method
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Embodiment 1
[0034] Example 1 Graphene Centrifugal Sedimentation Efficiency and Graphene Enrichment Efficiency of Graphene with / without Cell Organelles
[0035] (1) Seed germination and graphene exposure: soak the newly harvested seeds in 30% H 2 o 2 solution for 15 min, and then washed three times with deionized water to ensure that the seed surface is sterile. The seeds were then soaked in deionized water and stored in the dark at 30°C for 48 h. Finally, the soaked seeds were evenly displayed in a sterilized petri dish, and the bottom of the petri dish was covered with two layers of sterilized moist filter paper, and the petri dish was covered and placed in a light incubator at 30°C for 7 days. After germination was complete, it was transferred to a container containing 2 L of exposure solution with a graphene concentration of 0 μg / L.
[0036] (2) After 7 days of exposure, rice leaves were collected, 0.2 g was accurately weighed, homogenized and centrifuged to obtain chloroplast compo...
Embodiment 2
[0041] Subcellular distribution results of graphene in rice stems under different exposure times in Example 2
[0042] (1) Seed germination and graphene exposure: soak the newly harvested seeds in 30% H 2 o 2 solution for 15 min, and then washed three times with deionized water to ensure that the seed surface is sterile. The seeds were then soaked in deionized water and stored in the dark at 30°C for 48 h. Finally, the soaked seeds were evenly displayed in a sterilized petri dish, and the bottom of the petri dish was covered with two layers of sterilized moist filter paper, and the petri dish was covered and placed in a light incubator at 30°C for 7 days. After germination was complete, it was transferred to a container containing 2 L of exposure solution with a graphene concentration of 250 μg / L. At the same time, another group of blank control group was set up, that is, after the germination ended, it was transferred to 2L of graphene-free solution.
[0043] (2) After expo...
Embodiment 3
[0048] Subcellular distribution results of graphene in rice leaves under different exposure times in Example 3
[0049] (1) Seed germination and graphene exposure: soak the newly harvested seeds in 30% H 2 o 2 solution for 15 min, and then washed three times with deionized water to ensure that the seed surface is sterile. The seeds were then soaked in deionized water and stored in the dark at 30°C for 48 h. Finally, the soaked seeds were evenly displayed in a sterilized petri dish, and the bottom of the petri dish was covered with two layers of sterilized moist filter paper, and the petri dish was covered and placed in a light incubator at 30°C for 7 days. After germination was complete, it was transferred to a container containing 2 L of exposure solution with a graphene concentration of 250 μg / L. At the same time, another group of blank control group was set up, that is, after the germination ended, it was transferred to 2L of graphene-free solution.
[0050] (2) After e...
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