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mRNA synthesis process

Product name

Cat#

Template preparation

Hieff CanaceTM Plus High-Fidelity DNA Polymerase (Inquire)

10148ES

Hieff CloneTM Universal One Step Cloning Kit 

10922ES

dNTP Mix (25 mM each)

10125ES

FuniCut™ BsaI

15005ES

FuniCut™ XbaI

15033ES

In vitro transcription

HifairTM T7 High Yield RNA Synthesis Kit

10623ES

UCF.METM T7 RNA Polymerase GMP-grade(50 U/μL)(Inquire)

10624ES

T7 RNA polymerase (50 U/μL) (Inquire)

10618ES

NTP Set Solution (ATP, CTP, UTP, GTP, 100 mM each)

10133ES

UCF.METM Pyrophosphatase,Inorganic GMP-grade

10620ES

UCF.METM Murine RNase inhibitor GMP-grade

10621ES

Remove template DNA

UCF.METM Deoxyribonuclease I (DNase I) GMP-grade

10611ES

mRNA modification

UCF.METM mRNA Vaccinia Capping Enzyme GMP-grade

10614ES

UCF.METM mRNA Cap 2´-O-Methyltransferase GMP-grade

10612ES

GTP (100 mM)

10132ES

S-adenosylmethionine (SAM)(32mM)

10619ES

mRNA purification

Hieff NGSTM RNA Cleaner

12602ES

African swine fever (ASF) is an acute, severe and highly contagious infectious disease caused by African swine fever virus (ASFV) infecting domestic pigs or wild boars. Its morbidity and mortality can reach 100%, seriously endangering the global pig industry and causing incalculable economic losses. The World Organization for Animal Health (OIE) lists it as a reportable animal disease, and my country lists it as a Class I animal disease.

 

 

At present, there is no vaccine or effective treatment for African swine fever. Rapid and accurate diagnosis of African swine fever through laboratory diagnostic methods is crucial to preventing the spread of the disease. Among laboratory detection technologies, qPCR is an important tool for routine diagnosis of African swine fever recommended by OIE, and it is also the preferred detection technology under the current situation of African swine fever.

 

 

Figure 1. Yeasen African Swine Fever related qPCR Products

 

 

Product advantages:

1. Efficient and convenient operation - Master Mix, no tedious operation, one-step sample addition

2. High detection sensitivity - genetically modified antibody method to hot-start Taq enzyme, 3 copies/reaction can be detected stably

3. stability of fully premixed PCR solution(Mix+Primers+Probes) - the working solution premixed can be stored at 37℃ for 7 days, and remains stable performance after repeated freezing and thawing

4. batch-to-batch stability - 20 repeated experiments of 4 different batches, CV<1%

5. High blood tolerance - can tolerate anticoagulant samples (EDTA, sodium citrate) and 0.5% whole blood

6. Suitable for multiple platforms - Bio-Rad CFX96, ABI Q5 and Slan are all compatible

 

 

 

ASFV detection solution 1: UDG fully premixed qPCR solution, super stability

 

 

Product collocation:
1.MolPureTM Magnetic Swab Viral DNA/RNA Kit(Cat#18300)
2.Hieff UniconTM  TaqMan Multiplex qPCR Master Mix(UDG plus)(Cat#13171)

 

 

Product advantages:

1.UDG anti-pollution system

2. Super stability of fully premixed PCR solution(Mix+Primers+Probes)

3. High amplification efficiency and good repeatability

4. Multi-platform multi-system applicable

 

 

 

Case show:

 

Super stability of fully premixed PCR solution

Cat#13171 was prepared into a fully premixed PCR solution containing primer and probes, placed at 37°C for 7 days, and repeated freezing and thawing 15 times to amplify the ASF plasmid system. The results showed that storage at 37°C for 7 days had no effect on the Ct value and sensitivity, and the Ct value did not change significantly after repeated freezing and thawing for 15 times.