Molecular marker relevant to reproductive performance of chicken and application of molecular marker in breeding
A molecular marker and reproductive performance technology, applied in the field of molecular genetics, to solve problems such as unclear mechanism and function
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Embodiment 1
[0018] Example 1 Sequencing, sequence alignment and mutation site analysis of chicken BMPR-IB gene 233062 site
[0019] According to the published red jungle fowl sequence (GenBank Accession No: NC_006091.2; GI: 118136300), design a set of primers BMP10 (its sequence is shown in SEQ ID No.2 and SEQ ID No.3), this set of primers is It is designed for studying the mutation of chicken BMPR-IB gene exon 8 and part of intron 8. This set of primers respectively amplified a sequence of 232748bp~233303bp of the BMPR-IB gene of Jining hundred-day chicken, Wenshang reed chicken and Hailan brown layer chicken, and the length of the amplified fragment was about 556bp (such as figure 1 shown), the PCR products were sent to the biological company for purification and sequencing. BMP10F: 5'-CCCTTCTCAGTTGCTT-3'; BMP10R: 5'-CCAAGATTAGTCCCAAA-3'. The primer position is 232748bp-233303bp, and the annealing temperature is 47.4°C.
[0020] Using BioEdit software to compare the sequence homology...
Embodiment 2
[0023] Example 2 Polymorphism detected by chicken SspⅠ-RFLP and its association analysis with laying traits
[0024] 1 test material
[0025] 400 Jining hundred-day chickens, 528 Wenshang reed chickens and 208 Hailan brown layer hens, all came from the live gene bank of local chicken breed resources in Shandong Province. All of the above were randomly sampled, blood was collected from the wing vein, anticoagulated with ACD, and stored at -20°C.
[0026] 2 test method
[0027] 2.1 Extraction of chicken blood DNA
[0028] Chicken blood DNA was extracted by conventional phenol / chloroform method.
[0029] 2.2 Mutation site and primer information
[0030]Chicken BMPR-IB gene 233062 site is a C→T mutation, which contains the recognition sequence "AAT / ATT" of the Ssp I restriction endonuclease, and "C" does not have a mutation, that is, the type of "AAT / ACT" is recorded as "CC ", the amplified fragment cannot be cut by SspI endonuclease; "C" is mutated to "T", that is, the type ...
Embodiment 3
[0050] The expression analysis of embodiment 3 chicken BMPR-IB gene
[0051] 1 test material
[0052] The same batch was hatched, reared in the same environment, and the nutritional level was consistent. There were 3 19W, 23W, and 40W Jining hundred-day chickens, all of which came from the live gene bank of local chicken breed resources in Shandong Province.
[0053] Liver (Liver, L), hypothalamus (Hypothalamus, H), oviduct (Oviduct, S) and ovary (Ovary, O) tissues were collected.
[0054] 2 test method
[0055] 2.1 Extraction of tissue total RNA
[0056] Total RNA in tissue samples was extracted with Ultrapure RNA Extraction Kit (CWbio.Co.Ltd, Cat#CW0581). The experimental operation was carried out according to the product manual.
[0057] 2.2 Reverse transcription
[0058] HiFi-MMLVcDNA First Strand Synthesis Kit (CWbio.Co.Ltd, Cat#CW0744) was used for reverse transcription, and the experimental operation was performed according to the product instructions.
[0059] 2....
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