A kind of method, primer and kit for detecting blue light phototaxis of aphids
A phototaxis and aphid technology, applied in the field of agricultural biology, can solve problems such as high technical requirements, difficult operation, and inability to meet, and achieve the effects of avoiding heavy workload, high accuracy and improving efficiency.
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Embodiment 1
[0052] Cloning of opsin gene CRY1 from rape aphids (mainly Myzus persicae).
[0053] 1. Aphid total RNA extraction and cDNA reverse transcription
[0054] Use Trizol reagent to extract the total RNA of rape aphids, and the specific steps are as follows: (1) Take about 50 mg of the frozen sample in an ultra-low temperature refrigerator, pour it into a mortar, and grind it thoroughly. The powder was transferred to a clean centrifuge tube with 1 mL of Trizol reagent, shaken vigorously, then left at room temperature for 10 min, centrifuged at 12000 rpm at 4°C for 10 min, and the supernatant was transferred to a new centrifuge tube. (2) Add 0.2mL chloroform, shake for 30s, and place at room temperature for 10min. Centrifuge at 12000rpm at 4°C for 10min. (3) Take the upper aqueous phase to a new centrifuge tube, add 400 μL of isopropanol, mix well, place at room temperature for 10 minutes, centrifuge at 12,000 rpm at 4°C for 10 minutes, and discard the supernatant. (4) Add 1 mL o...
Embodiment 2
[0089] In order to facilitate detection and application, this embodiment provides a primer for detecting blue light phototaxis of rape aphids, which includes primers shown in Seq ID No.5-6.
[0090] Using the cDNA of the rape aphid provided in Example 1 as a template, and the sequence Seq ID No.5-6 as a primer, the full-length sequence of the rape aphid opsin gene CRY1 can be obtained by one-time PCR amplification, and the PCR reaction system is as follows:
[0091] wxya 2 o
13.6μL
10×Buffer
2.0 μL
dNTP (2.5mM)
1.6μL
cDNA
1.0 μL
Upstream primer Seq ID No.5 (10μM)
0.8μL
Downstream Primer Seq ID No.6 (10μM)
0.8μL
Taq enzyme
0.2 μL
overall system
20.0 μL
[0092] The conditions of the PCR amplification reaction were: pre-denaturation at 94°C for 5 minutes; 30 cycles at 94°C for 30s, 55°C for 30s, and 72°C for 30s; and extension at 72°C for 10 minutes.
[0093] After sequencing and com...
Embodiment 3
[0096] Bioinformatics Analysis and Discrimination of Opsin CRI of Rapeseed Aphid
[0097] 1. Analysis of the Conserved Domain of CRY1 Opsin in Rapeseed Aphid
[0098] The conserved structure analysis of the opsin sequence of rape aphid was completed by SMART (http: / / smart.embl-heidelberg.de / ). Using Smart analysis, the results showed that CRY1 opsin has DNA photolyase protein family and DNA photolyase FAD binding protein family conserved domains, but no binding site ( figure 2 ).
[0099] 2. Prediction of transmembrane structure and subcellular localization of CRY1 opsin in rape aphid
[0100] Using TMHMM Server v.2.0 to analyze the transmembrane region of the protein sequence (http: / / www.cbs.dtu.dk / services / TMHMM / ) to predict the transmembrane structure of the rape aphid opsin. The analysis showed that no transmembrane structure was found for the CRY1 opsin of the rape aphid, and the subcellular location was in the cytoplasm (such as image 3 As shown, in the figure: A: ...
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