A rapid method for identifying the authenticity and purity of edible sunflower hybrid sh363
A technology of SH363 and sunflower, which is applied in the field of agricultural molecular biology, can solve the problems of being easily affected by climate and cultivation conditions, taking a long time, and untimely guidance, so as to achieve accurate and reliable detection and identification of authenticity and purity, and the measurement results Accurate and simple operation steps
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0071] The method for quickly identifying the authenticity and purity of the edible sunflower hybrid SH363 of the present invention comprises the following steps:
[0072] (1) Take the sunflower true leaves planted by the edible sunflower hybrid SH363 to be tested and the standard sunflower seeds A436 and R1843 as materials, and use the CTAB method to extract the genomic DNA of the above-mentioned edible sunflowers. The specific steps are as follows:
[0073] a) Take 10 mg (about 1 cm) of the edible sunflower true leaf 2 ) was placed in a 2mL centrifuge tube with grinding beads (D=0.6mm stainless steel beads), placed in liquid nitrogen for pre-freezing, and the pre-frozen centrifuge tube was placed in a grinder and ground for 30 s at 30 Hz, then Quickly transfer the centrifuge tube to stand-by in liquid nitrogen;
[0074] b) Take out the centrifuge tube in step a) and add 1000 μL of the preheated mixture of CTAB buffer and mercaptoethanol with a volume ratio of 20:1, shake an...
Embodiment 2
[0104] The method for quickly identifying the authenticity and purity of the edible sunflower hybrid SH363 of the present invention comprises the following steps:
[0105] (1) Take the sunflower true leaves planted by the edible sunflower hybrid SH363 to be tested and the standard sunflower seeds A436 and R1843 as materials, and use the CTAB method to extract the genomic DNA of each of the above-mentioned edible sunflowers. The steps are as follows:
[0106] a) Take 10 mg (about 1 cm) of the edible sunflower true leaf 2 ) was placed in a 2mL centrifuge tube with grinding beads (D=0.6mm stainless steel beads), placed in liquid nitrogen for pre-freezing, and the pre-frozen centrifuge tube was placed in a grinder and ground for 30 s at 30 Hz, then Quickly transfer the centrifuge tube to stand-by in liquid nitrogen;
[0107] b) Take out the centrifuge tube in step a) and add 1000 μL of the preheated mixture of CTAB buffer and mercaptoethanol with a volume ratio of 20:1, shake and...
Embodiment 3
[0136] The method for quickly identifying the authenticity and purity of the edible sunflower hybrid SH363 of the present invention comprises the following steps:
[0137] (1) Take the sunflower true leaves planted by the edible sunflower hybrid SH363 to be tested and the standard sunflower seeds A436 and R1843 as materials, and use the CTAB method to extract the genomic DNA of each of the above-mentioned edible sunflowers. The steps are as follows:
[0138] a) Take 10 mg (about 1 cm) of the edible sunflower true leaf 2 ) was placed in a 2mL centrifuge tube with grinding beads (D=0.6mm stainless steel beads), placed in liquid nitrogen for pre-freezing, and the pre-frozen centrifuge tube was placed in a grinder and ground for 30 s at 30 Hz, then Quickly transfer the centrifuge tube to stand-by in liquid nitrogen;
[0139] b) Take out the centrifuge tube in step a) and add 1000 μL of the preheated mixture of CTAB buffer and mercaptoethanol with a volume ratio of 20:1, shake and...
PUM
| Property | Measurement | Unit |
|---|---|---|
| length | aaaaa | aaaaa |
| weight | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


