Method for extracting total DNA from milk
A milk and milk sample technology, applied in the field of dairy cow molecular biology, can solve the problems of low DNA purity and concentration of milk samples
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Embodiment 1
[0044] 1. Total DNA extraction, including the extraction of total DNA from milk and the extraction of total DNA from cow blood;
[0045] (1) Extraction of milk sample total DNA, the steps are as follows:
[0046] 1) Preparation before sampling: Scrub the teats of cows with iodine, dry the iodine on the teats with a clean warm cloth, discard the first 2-3 handfuls of milk squeezed out, and then use a milking machine or artificial milking to obtain milk samples;
[0047] 2) Sampling: Add 1ml of somatic cell fixative and 0.5ml of 20% potassium dichromate in the centrifuge tube in advance as preservatives, put the collected milk sample into the centrifuge tube to 50ml, centrifuge at 2500 rpm, 4°C for 30 minute;
[0048] 3) Discard the upper milk fat and the middle emulsion of the centrifuge tube in step 2), keep the bottom sediment, add 1ml sterilized phosphate buffer to the bottom, beat the bottom sediment to suspend and transfer to a 1.5ml centrifuge tube, at 3500 rpm / min, ce...
Embodiment 2
[0080] This example has randomly taken the fresh milk sample of 5 dairy cows from the Wuhu Pasture of Wuhan Huierkang Yangzijiang Dairy Co., Ltd., Wuhan City, Hubei Province, extracted the total DNA in the milk sample according to the method of the present invention, and got 4 μ L of milk sample DNA and diluted 50 After doubling, the OD was measured on a Beckman-DU 800 UV spectrophotometer 260 / 280 value and DNA concentration. The concentration calculation formula used is: A260*dilution factor*50ug / ul.
[0081] Get the data shown in Table 1:
[0082] Table 1 Milk sample DNA purity and concentration determination results
[0083] milk sample number
[0084] As can be seen from Table 1, DNA purity OD 260 / 280 If the value is within the range of 1.8-2.0, the DNA purity meets the requirements. Concentrations vary prominently between individuals due to differences in somatic cells contained in milk samples from different individuals.
Embodiment 3
[0086] PCR detection of DNA extraction and purification effect:
[0087] In this example, total DNA extracted from milk and total DNA extracted from blood were used as PCR templates to amplify exon 9 of the growth hormone receptor (GHR) gene, and the amplification effects were compared and detected.
[0088] 1. Primer sequence
[0089] Forward primer: 5'-TAGGAGTTCCTTTTTAGAGGATAGGTGC-3'
[0090] Reverse primer: 5'-GCCTTGTGGAGAAGTTGACAAA-3'
[0091] References for primers used Blott S, Kim J J, Moisio S, et al. Molecular Dissection of a QuantitativeTrait Locus: A Phenylalanine-to-Tyrosine Substitution in the Transmembrane Domain of the BovineGrowth Hormone Receptor Is Associated With a Major Effect on Milk Yield and Composition . J. Genetics, 2003, 163: 253-266.
[0092] 2. PCR reaction system
[0093] Add to the PCR reaction system with a total volume of 10 μl:
[0094] wxya 2 O 7.2 μl
[0095] 10*PCR buffer 1.0μl
[0096] 10mmol / L dNTPs 0.3μl
[0097] 2.5U Taq enzyme 0....
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