UIMC1 gene mutation site detection kit and application thereof
A detection kit and gene technology, applied in the field of UIMC1 gene mutation site detection kits, can solve the problems of different degrees of radiation damage, adverse reactions, poor treatment effects, etc., and achieve the effect of low cost and high efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0021] 1) Sample collection, irradiation and chromosome aberration analysis
[0022] Collect peripheral blood from healthy adult males aged 20-30, give 0, 2Gy 60 Co gamma ray irradiation. Chromosomal aberration analysis was performed on samples irradiated with 2Gy γ-rays, and the population was divided into susceptible group, general group and non-susceptible group. Chromosomes were harvested after blood samples were cultured for 52 hours after irradiation, and slides were prepared. 200 metaphases were analyzed per sample.
[0023] 2) Genomic DNA extraction from peripheral blood
[0024] Genomic DNA was extracted from the 0Gy irradiated samples of the susceptible group and the non-susceptible group. Genomic DNA extraction kit from Beijing Tiange Biochemical Technology Co., Ltd. was used to extract genomic DNA from whole blood according to the product instructions. See the instructions for specific steps. The A260 / 280 of the sampled nucleic acid quantitative detection is b...
Embodiment 2
[0032] 1) Using Beijing Tiange Biochemical Technology Co., Ltd. Blood Genomic DNA Extraction Kit (non-centrifugal column type; catalog number: DP319), perform human whole blood genome (source is the same as step 1) in Example 1) DNA extraction according to the product instructions.
[0033] 2) Using the amplification primer pair of SEQ ID NO.3 and SEQ ID NO.4, the specific reaction system (5 μl reaction system includes 0.95 μl H 2 O, 0.625μl PCR Buffer (10×), 0.325μl MgCl 2 (25mM), 1μl dNTP (2.5mM), 1μl primer, 0.1μl HotstarTaq (5U / μL)) for PCR reaction, the reaction program is: 94°C, 15min; [94°C, 20sec, 56°C, 30sec] 45 cycles ; 72°C, 4min. The reaction product was stored at 4°C.
[0034] 3) Use SAP reaction solution (2μl SAP reaction solution includes 1.53μl H 2 0, 0.17 μl SAP Buffer (10×), 0.3 μl SAP enzyme (1 U / μL)) to treat the reaction product of step 2), the treatment program is: 37° C., 40 min; 85° C., 5 min. The processed product was stored at 4°C.
[0035] 4) us...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 
