SV40LTAE1A residual DNA kit and application

The invention discloses an SV40LTAamp and a method for implementing the SV40LTAamp; the E1A residual DNA kit comprises the following components: SV40LTAamp, E1A residual DNA, E1A residual DNA and E1A residual DNA, an E1A DNA quantitative reference substance, and SV40LTAamp; the kit comprises the fol...

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Main Authors ZHANG TIANYANG, ZHENG MENGTAO, FAN PENGCHENG, LI ZHA, CAI YUQING, LIU LIMEI
Format Patent
LanguageChinese
English
Published 25.04.2023
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Abstract The invention discloses an SV40LTAamp and a method for implementing the SV40LTAamp; the E1A residual DNA kit comprises the following components: SV40LTAamp, E1A residual DNA, E1A residual DNA and E1A residual DNA, an E1A DNA quantitative reference substance, and SV40LTAamp; the kit comprises the following components: E1A Primer MIX, qPCRReaction Buffer and a DNA (Deoxyribose Nucleic Acid) diluent. According to the method, a vortex oscillator is used for oscillation for 5-10 seconds during dilution, and then rapid centrifugation is performed for 4-8 seconds at the speed of 800-1000 rpm, so that DNA fragments with the size of 150-250 bp can be fully and uniformly dispersed in a dilution tube, and the influence of winding of the DNA fragments on the reaction efficiency is reduced. In addition, SV40LTAamp is adopted; the E1A PrimerMIX accounts for 15-20% of the total volume of the qPCR reaction liquid, so that a plurality of initiation points exist in the PCR reaction, and the chain extension efficiency of the PC
AbstractList The invention discloses an SV40LTAamp and a method for implementing the SV40LTAamp; the E1A residual DNA kit comprises the following components: SV40LTAamp, E1A residual DNA, E1A residual DNA and E1A residual DNA, an E1A DNA quantitative reference substance, and SV40LTAamp; the kit comprises the following components: E1A Primer MIX, qPCRReaction Buffer and a DNA (Deoxyribose Nucleic Acid) diluent. According to the method, a vortex oscillator is used for oscillation for 5-10 seconds during dilution, and then rapid centrifugation is performed for 4-8 seconds at the speed of 800-1000 rpm, so that DNA fragments with the size of 150-250 bp can be fully and uniformly dispersed in a dilution tube, and the influence of winding of the DNA fragments on the reaction efficiency is reduced. In addition, SV40LTAamp is adopted; the E1A PrimerMIX accounts for 15-20% of the total volume of the qPCR reaction liquid, so that a plurality of initiation points exist in the PCR reaction, and the chain extension efficiency of the PC
Author FAN PENGCHENG
LI ZHA
ZHANG TIANYANG
ZHENG MENGTAO
LIU LIMEI
CAI YUQING
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– fullname: LIU LIMEI
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DocumentTitleAlternate 一种SV40LTA&E1A残留DNA试剂盒及应用
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Snippet The invention discloses an SV40LTAamp and a method for implementing the SV40LTAamp; the E1A residual DNA kit comprises the following components: SV40LTAamp,...
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SubjectTerms BEER
BIOCHEMISTRY
CHEMISTRY
COMPOSITIONS OR TEST PAPERS THEREFOR
CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES
ENZYMOLOGY
MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS
METALLURGY
MICROBIOLOGY
MUTATION OR GENETIC ENGINEERING
PROCESSES OF PREPARING SUCH COMPOSITIONS
SPIRITS
VINEGAR
WINE
Title SV40LTAE1A residual DNA kit and application
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