Kit for rapid detection of authenticity of edible sunflower hybrid sh363
A technology of SH363 and kit, which is applied to the determination/inspection of microorganisms, biochemical equipment and methods, etc., can solve the problems of time-consuming, easy to be affected by climate and cultivation conditions, no evaluation criteria, etc., and achieves simple operation steps, Efficient variety identification and stable identification results
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Embodiment 1
[0057] The kit for rapid detection of the authenticity of the edible sunflower hybrid SH363 described in this embodiment includes separately packaged primer solutions, reaction solutions and DNA polymerase parts, wherein,
[0058] The primer in the primer liquid part is primer SR-366, and the SR-366 primer is:
[0059] SR-366-F: 5'-AACCAACTGAGCATTCTTGTGA-3',
[0060] SR-366-R: 5'-GCGCTAGGTTAAAGAGGACAAA-3'.
[0061] The formula of each described kit is:
[0062] Primer solution, 0.2μM, 1μL;
[0063] Taq DNA polymerase, 2.5units, 0.5μL;
[0064] 10× Contains Mg 2+ Amplification buffer, 2mM, 2.5μL;
[0065] dNTPs, 2.5mM, 2μL;
[0066] wxya 2 O, 17 μL.
[0067] The method for rapidly detecting the authenticity of the edible sunflower hybrid SH363 by using the above kit comprises the following steps:
[0068] (1) Using the improved CTAB method to extract the genomic DNA of the sunflower grown by the edible sunflower hybrid SH363 and its parent standard sunflower seeds A436...
Embodiment 2
[0091] The kit for rapid detection of the authenticity of the edible sunflower hybrid SH363 described in this embodiment includes separately packaged primer solutions, reaction solutions and DNA polymerase parts, wherein,
[0092] The primer in the primer liquid part is primer SR-495, and the SR-495 primer:
[0093] SR-495-F: 5'-CCAGGATTAGGTAGCTTAGTTCG-3',
[0094] SR-495-R: 5'-GCGATCTGAGGTTGACTCGT-3'.
[0095] The formula of each described kit is:
[0096] Primer solution, 0.2μM, 1μL;
[0097] Taq DNA polymerase, 2.5units, 0.5μL;
[0098] 10× Contains Mg 2+ Amplification buffer, 2mM, 2.5μL;
[0099] dNTPs, 2.5mM, 2μL;
[0100] wxya 2 O, 17 μL.
[0101] The method for rapidly detecting the authenticity of the edible sunflower hybrid SH363 by using the above kit comprises the following steps:
[0102] (1) Using the improved CTAB method to extract the genomic DNA of the sunflower grown by the edible sunflower hybrid SH363 and its parent standard sunflower seeds A436 and...
Embodiment 3
[0125] The kit for rapid detection of the authenticity of the edible sunflower hybrid SH363 described in this embodiment includes separately packaged primer solutions, reaction solutions and DNA polymerase parts, wherein,
[0126] The primer in the primer solution part is primer SR-1067, and the SR-1067 primer:
[0127] SR-1067-F: 5'-CGTCAACTAATGCTGTCCTGATG-3',
[0128] SR-1067-R: 5'-TCGGATATGATGCTGCTAAAGGT-3'.
[0129] The formula of each described kit is:
[0130] Primer solution, 0.2μM, 1μL;
[0131] Taq DNA polymerase, 2.5units, 0.5μL;
[0132] 10× Contains Mg 2+ Amplification buffer, 2mM, 2.5μL;
[0133] dNTPs, 2.5mM, 2μL;
[0134] wxya 2 O, 17 μL.
[0135] The method for quickly identifying the authenticity of the edible sunflower hybrid SH363 using the kit comprises the following steps:
[0136] (1) Using the improved CTAB method to extract the genomic DNA of the sunflower grown by the edible sunflower hybrid SH363 and its parent standard sunflower seeds A436 and...
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