Molecular marking method for pig litter size
A molecular marker, litter size technology, applied in biochemical equipment and methods, microbial determination/inspection, etc., to achieve the effects of simple operation, easy amplification, and improved accuracy
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2010-07-07
- Estimated Expiration
- Not applicable · inactive patent
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Abstract
Description
technical field
[0001] The invention belongs to the technical field of animal gene polymorphism, in particular to the polymorphism of sex hormone binding globulin (SHBG) gene of pigs. Background technique
[0002] Sex hormone-binding globulin (Sex Hormone-Binding Globulin, SHBG), also known as testosterone-estradiol-binding globulin, SHBG is a carrier for transporting sex hormones. The arrival of animal sex hormones to target tissues is regulated by SHBG in the blood. SHBG is A glycoprotein expressed in liver cells, this protein specifically binds to and participates in the transport of sex hormones, and regulates the concentration of biologically active sex hormones in the blood. Under physiological conditions, a dynamic balance exists between the rapid dissociation of the sex hormone-binding globulin (SHBG) complex and the association of free sex hormones with SHBG, which are protected from vascular adsorption, biological and chemical Destruction and rapid degradation, on...
Examples
Embodiment
[0053] A specific operation method of a molecular marker method for pig litter size traits is as follows:
[0054] (1) Collection of ear tissue samples
[0055] On the day of the piglet's birth, about 0.2 grams of the pig's ear margin tissue was collected with pig ear forceps, put into a 1.5ml centrifuge tube, poured about 1ml of 75% alcohol, and then stored in a -20°C refrigerator for later use.
[0056] (2) Genomic DNA extraction
[0057] Take out the ear margin tissue from the refrigerator, cut it into pieces with scissors, and pour 600ul of DNA tissue extraction solution. The formula of the DNA tissue extraction solution is shown in Table 1, and the extraction solution is ready for use. Then put it in a warm bath at 55°C for 12 hours, then add 600ul of Tris saturated phenol, shake it up and down for 15 minutes, and centrifuge for 10 minutes in a low-temperature high-speed centrifuge with a speed of 12000 rpm; take out the supernatant with a 1ml pipette To a sterilized 1....