Method for discriminating overwintering-recovery period boundary of overwintering cyanobacteria
A recovery period and boundary technology, which is applied in the field of distinguishing the boundary of overwintering cyanobacteria overwintering recovery period, can solve the problems of pseudovacuum easy to collapse, etc., and achieve good repeatability, repeatability and accuracy
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Embodiment 1
[0038] 1. Sample Collection and RNA Extraction
[0039] From November 2012 to July 2013, water samples from Meiliang Bay (N2) in Taihu Lake were collected monthly. At the sampling point, 100ml of water samples were immediately filtered with GF / C filter membranes, quickly stored in liquid nitrogen, and brought back to the laboratory for storage. Store at -70°C until RNA extraction. Take 40 mL of Microcystis grown indoors in logarithmic growth phase (the medium for indoor cultured Microcystis is BG-11, the culture temperature is 30 °C, and the light intensity is 30 μE·(m 2 s) -1 , photoperiod of 12 h:12 h), the algal cells were collected by centrifugation, and then RNA was extracted. RNA was extracted from field samples and indoor samples using RNeasy Plant Mini Kit from QIAGEN. The field samples and indoor samples were transferred to the corresponding numbered lysis tube B (Lysing MatrixB, diameter 0.1 mm), and then 500 μL Buffer RLT was added to each lysis tube B, and the l...
Embodiment 2
[0046] 1. Sample Collection and RNA Extraction
[0047] From November 2012 to May 2013, water samples from the center of Taihu Lake (S2) were collected every month. At the sampling point, 100 mL of water samples were immediately filtered with GF / C membranes, quickly stored in liquid nitrogen, and brought back to the laboratory for storage. Store at -70°C until RNA extraction. Take 40 mL of Microcystis grown indoors in logarithmic growth phase (the medium for indoor cultured Microcystis is BG-11, the culture temperature is 30 °C, and the light intensity is 30 μE·(m 2 s) -1 , and the photoperiod is 12h-12h), the algal cells were collected by centrifugation, and then RNA was extracted. The extraction of RNA from field samples and indoor samples was performed using RNeasy Plant Mini Kit from QIAGEN. The field samples and indoor algae were transferred to the corresponding numbered lysis tube B (Lysing MatrixB, diameter 0.1 mm), and then 500 μL Buffer RLT was added to each lysis ...
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