SSR multiple detection primer, kit and method for pithecellobium clypearia variety identification
A variety identification and multiple detection technology, which is applied in biochemical equipment and methods, microbial measurement/inspection, recombinant DNA technology, etc., can solve the problem that there is no multiple SSR detection technology system for monkey earring variety identification, and save experimental costs , Reagent saving, good economical effect
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Embodiment 1
[0044] (1) The 15 SSR markers of monkey earrings are optimized into 7 combined triple or double detection technology systems
[0045] Based on the 456 SSR-labeled primer sequences developed by our laboratory in the early stage, taking into account that the primers do not interfere with each other (not paired with each other), the PCR amplification program is the same, the length range of the amplified fragment is different and the concentration of the amplified product (the peak height of the detection ) and other factors, select 15 highly polymorphic markers with polymorphic information content (polymorphic information content, PIC) higher than 0.5 and optimize them as 7 combinations of triple or double detection, and the 5' end of the forward primer of the same combination Modified with different fluorophores (FAM, HEX, ROX or TAM); the specific 7 combinations (the asterisks indicate primer-modified fluorophores) are:
[0046] Marker combination A: ARCeSSR266(*HEX), ARCeSSR1...
Embodiment 2
[0078] Example 2: Identification of 20 varieties (cutting clones) of monkey earrings to be tested based on SSR molecular markers
[0079] (1) DNA extraction of monkey earring species. The 20 varieties to be inspected still come from Huadu Cutting Nursery of Guangdong Province (23°24'12"N, 113°13'06"E). About 3g of young leaves of each variety are collected, which can be temporarily refrigerated or long-term frozen.
[0080] DNA extraction from leaf samples was performed using a modified CTAB (cetyltrimethylammonium bromide) method. Concrete method is with (2) step (1) among the embodiment 1.
[0081] (2) Multiplex polymerase chain reaction (PCR) and detection of 15 SSR molecular markers. The 15 SSR molecular markers optimized based on the present invention are divided into 7 groups of triple or double detection techniques (marker grouping and primer modification fluorescence are the same as (1) in Example 1), using the DNA extracted in step (1) as a template, Perform PCR amp...
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