Molecularly Specific Marker Primers and Detection Methods of Cherry Blossom Variety "Guanshan"
A labeled primer and specific technology, applied in the direction of DNA / RNA fragments, recombinant DNA technology, etc., can solve the problems of difficult identification of phenotypic characteristics, application and promotion of garden plants, and difficulty in breeding new varieties, and achieve the effect of simple methods
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0038] (1) Extraction of Genomic DNA of Cherry Blossom Varieties:
[0039] Take 0.01g of the young leaves of the cherry blossom variety to be tested, add liquid nitrogen and grind them thoroughly, and use the SDS-CTAB method to extract the genomic DNA. After multiple extractions, the crude genomic DNA extract of the cherry blossom variety is obtained. The crude DNA was purified by Magabio Nucleic Acid Purification Kit (Bioer, Hangzhou, China), and detected by 1.5% agarose gel electrophoresis and DNA / RNA UV spectrophotometer (GeneQuant Pro, GE Healthcare). Integrity, Purity and Concentration. DNA samples with OD260 / OD280>1.8 were used for subsequent PCR amplification. DNA extracts were stored in a -20°C refrigerator for later use.
[0040] (2) Design specific PCR amplification primers, the sequence of the primer pair is:
[0041] The upstream primer: 5′-TGAGTCCAAACCGGACCAAGTT-3′ and the downstream primer: 5′-GACTGCGTACGAATTTGAAAAGCT-3′ were synthesized by Shanghai Bioenginee...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


