Method for extracting total DNA (Deoxyribose Nucleic Acid) of mixed chironomidae insect ecdysis on surface of water body
A water surface, mosquito technology, applied in the biological field, to achieve the effect of high purity and high DNA concentration
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Embodiment 1
(1): Go to the downwind of rivers and lakes, especially the banks with a little white foam, to collect chironomididae pupa skins.
[0025] (2): soak the collected chironomid pupa skin with 95% alcohol for 5 minutes, soak twice, and then rinse with distilled water three times to remove impurities on the pupa skin.
[0026] (3): soak the pupal skin with physiological saline for two hours to restore the activity of the remaining cells on the pupal skin to facilitate DNA extraction.
[0027] (4): Put the pupa skin into a 37° water bath and keep it at a constant temperature for 2 hours.
[0028] (5): put the treated pupa skin into the mortar, add dissociation solution and fully grind; The composition of described dissociation solution (200 ml) is as follows (W / W):
CTAB 4g final concentration 2%
SDS 1g final concentration 0.5%
0.5M EDTA 8 ml final concentration 0.02M
1M Tris-HCl 20 ml final concentration 0.1M
5M NaCl 40 ml final concentration 1M
β-Mercaptoethanol 0.2 ml f...
Embodiment 2
PCR reaction
(1) PCR reaction system:
Total system 50 ul: ddH 2 O 32.4 ul, 10ⅹ PCR Buffer 5 ul, dNTPs (2.5 mmol / L) 4ul, universal primers LCO and HCO (10 u mol / L) 2 ul each, Taq enzyme (500 U, 2.5 U / ul) 0.6 ul, DNA template 4 ul.
[0036] (2) PCR reaction conditions:
Pre-denaturation at 94°C for 5 min; denaturation at 94°C for 10 s; annealing at 55°C for 30 s; extension at 72°C for 60 s; 35 cycles; extension at 72°C for 10 min; storage at 4°C.
[0037] (3) Spectrophotometric detection of DNA, and electrophoresis detection of PCR products with 1% agarose gel.
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