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34results about How to "Unaffected by environmental conditions" patented technology

SSR (Simple Sequence Repeat) molecular marking method for identifying variety authenticity and/ or variety purity of high-quality transgenic hybrid cotton CCRI (Chinese cotton research institute) 70

The invention discloses an SSR (Simple Sequence Repeat) molecular marking method for identifying variety authenticity and/ or variety purity of high-quality transgenic hybrid cotton CCRI (Chinese cotton research institute) 70, which comprises the following steps: extracting genomic DNA (Deoxyribose Nucleic Acid) from a cotton hybrid 'CCRI 70' and the patient seed or the young seedling leaves thereof; taking the genomic DNA extracted in step one as a template, and carrying out PCR (Polymerase Chain Reaction) amplification by an SSR primer; carrying out gel electrophoresis on an amplified product; and analyzing an electrophoresis result, wherein a seed or a signal plant is identified as a real hybrid if the seed or the signal plant has special bands of parents, and is identified as a false hybrid if any one band lacks. The SSR molecular marking method has the advantages of good repeatability, high polymorphism, stable hereditary, stable and reliable detection result and low cost, is free from the influence of environmental condition, is quick and accurate, is simple and convenient to operate and is favorable for quickly detecting on a large scale.
Owner:INST OF COTTON RES CHINESE ACAD OF AGRI SCI

Molecular marker identification method for bacterial angular leaf spot resistant gene of cucumber

The invention relates to a molecular marker identification method for the bacterial angular leaf spot resistant gene of cucumbers, which comprises: performing polymerase chain reaction (PCR) amplification by using the DNA of a cucumber variety or strain of which the bacterial angular leaf spot resistance is unknown as a template and chimpanzee sanctuary and wildlife conservation trust (CSWCT)24A as a primer; detecting the product of the amplification by electrophoresis in 3-percent gelose gel or 7.5-percent denaturant polyacrylamide gel; and if the band type obtained by amplification is consistent with the band of a known bacterial angular leaf spot resistant cucumber Dongnong 803, determining the cucumber variety or strain of which the bacterial angular leaf spot resistance is unknown as a bacterial angular leaf spot resistant variety or strain. The PCR amplification process comprises: pre-denaturing at 94 DEG C for 5 minutes, denaturing at 94 DEG C for 30 seconds, annealing at 57 DEG C for 1 minute, circulating for 35 times, extending at 72 DEG C for 1 minute, extending at 72 DEG C for 10 minutes, and storing at 4 DEG C. The method is used for identifying the bacterial angular leaf spot resistant gene of cucumbers.
Owner:NORTHEAST AGRICULTURAL UNIVERSITY

Primer sequence for identifying resistance of cucumber against alternaria cucumerina and identification method thereof

The invention discloses a primer sequence for identifying resistance of cucumber against alternaria cucumerina and an identification method thereof. The primer sequence comprises nucleotide sequences shown as SEQ ID No.1 and SEQ ID No.2 in a sequence table. The method for identifying the resistance of the cucumber against the alternaria cucumerina comprises the following steps of: (1) extracting genomic DNA of the cucumber; (2) performing polymerase chain reaction (PCR) amplification by taking the nucleotide sequences shown as SEQ ID No.1 and SEQ ID No.2 in the sequence table as primers; (3) performing gel electrophoresis analysis on the amplification product; and (4) identifying the resistance of the cucumber against the alternaria cucumerina according to the relative position of each identified sample on a gel strip. By evaluating the resistance of the constructed segregation population of generation F2 and cucumber germplasm resources against the alternaria cucumerina with the primer sequence of the invention, the coincidence rates for the result and artificial inoculation evaluation reach 95.04 percent and 94.74 percent respectively; the linkage genetic distance with the alternaria cucumerina resistance gene is 4.96cm; and the primer sequence has the advantages of high speed, accuracy and freedom from environmental condition and the like, and has great application value for screening the resistance of the resources in the cucumber breeding.
Owner:TIANJIN RES INST OF VEGETABLE

An optical soliton generation device and method with adjustable center frequency

InactiveCN104375353BSolve the problem of adjustable frequencySimple methodNon-linear opticsMicro nanoTransfer procedure
The invention relates to the field of interaction of laser and matter in strong-field physics, in particular to an optical soliton generation device and method with an adjustable center frequency. The optical soliton generation device comprises a laser, an action structure and a receiver. The method includes the steps that S1, an interval d between periodical medium planes is selected, the size delta of a periodical medium is obtained according to the formula that d=2*delta, and a periodical micro-nano structure is formed; S2, short-period ultra-short laser pulse is introduced, and the laser pulse is transmitted in the medium; S3, the reflection electric field and the transmission electric field generated when the pulse is transmitted in the periodical micro-nano structure are recorded respectively; S4, the recorded data are processed and analyzed, and then soliton pulse is obtained. By changing the size of the medium in the periodical micro-nano structure, the transmission process of the pulse in the micro-nano structure is affected, the final transmission electric field is further affected, and solitons of different frequencies are obtained. The optical soliton generation method is simple, easy to implement, free of influences of environment conditions and good in stability and repeatability of the system, and well realizes the adjustable center frequency of the optical solitons.
Owner:SHANTOU UNIV

DNA molecular identification method of Haliotis sieboldii and Haliotis discus Hannai hybrid

The invention discloses a DNA molecule identification method of coenospecies of Xishi abalone and Haliotis discus hannai Ino, relating to the DNA molecule marker detection of an abalone, in particular to a method for carrying out molecule identification to the authenticity of the coenospecies of an interspecific coenospecies generation of the Xishi abalone and the Haliotis discus hannai Ino by utilizing a molecule marker technology (microsatellite technology). The invention provides a DNA molecule identification method of the coenospecies of the Xishi abalone and the Haliotis discus hannai Ino by using microsatellite molecular marker, which has the advantages of high polymorphism, stable heredity and not being affected by environment conditions, etc, and can identify the authenticity of the coenospecies of the interspecific coenospecies generation of the Xishi abalone and the Haliotis discus hannai Ino during the large scale interspecific hybridization species production process of the Xishi abalone and the Haliotis discus hannai Ino. The genome DNA of the coenospecies generation of the Xishi abalone and the Haliotis discus hannai Ino is extracted by adopting a phenol chloroform method and PCR amplification reaction is carried out by taking the extracted genome DNA as a template to obtain the amplification product; gel electrophoresis and dyeing are carried out to the amplification product, and the map is compared; and comparison is carried out according to the electrophoresis result and the provided standard map.
Owner:XIAMEN UNIV
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