Dermatophagoides farina allergen Der f9 gene coded protein and application thereof
A gene encoding, dust mite technology, applied in the field of molecular biology, can solve problems such as difficult standardization
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[0012] 1 Amplification of Der f9 gene and synonymous mutation of NcoI site
[0013] Two pairs of primers were analyzed, designed and synthesized for cloning the active part of Der f9 gene and the NcoI in the synonymous mutation sequence, named F 6 :5′-CT CCATGG ATCATAGTGAAGAACAAGCTATTC-3' (underlined is the Nco I restriction site); R 6 : 5′-GTTCATTGATCATCCAAGGAAAACG-3′; F 7 :
[0014] 5′-CGTTTTCCTTGGATGATCAATGAAC-3′; R 7 :5′-TC CTCGAG AACTGTA
[0015] TTCGAAATGATCCAATTACG-3' (Xho I restriction site is underlined). Using plasmid pCold TF-Der f9 as template, F 6 -R 6 Or F 7 -R 7 Perform PCR with primers, the total reaction volume is 50μL, the specific composition is: 5μL of 10×PyrobestPCRBuffer, 0.5μL ofTaKaRa DNA Polymerase, 8μL of dNTP, 1μL of F 6 or F 7 ,1μLof R 6 or R 7 ,0.5μL of pCold TF-Der f9,34μL of ddH 2 O. The reaction conditions are as follows: denaturation at 94°C for 2 minutes and then enters the cycle. The cycle parameters are 94°C for 30s, 56°C for 30s, 72°C for 30s...
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