Molecular diagnostics is a technology used for diagnosing and monitoring diseases at the molecular level. It allows for the detection of diseases and their pathogenic factors with high precision and sensitivity, even before symptoms appear. Molecular diagnostics typically involves extracting DNA or RNA from patient samples (such as blood, urine, or tissue) and then using molecular biology techniques such as PCR (polymerase chain reaction) for amplification and analysis.
Pair
Lot
Product name
Classes
MethodAdvantage
Application
On Trial
HS23
Taq antibody I
Ab
Multi-table blocking, used in conjunction with Taq polymerase.
RT-PCR, HS PCR
HS18001
One step RT-qPCR Super mix I
Blend
High sensitivity, compatible with multiple amplification systems.
RT-PCR, HS PCR
HS18002
One step RT-qPCR Super mix II
Blend
Fast, convenient, efficient
RT-PCR, HS PCR
HS24-01
Taq-Ab qPCR Mix (No Rox)
Blend
Hot start (antibody modification), multiplex rapid, without ROX.
RT-PCR, HS PCR
HS17
Hot start Taq V2
Enzyme
1) Antibody-modified enzyme, rapid heat activation at 95°C for 30 seconds. 2) Good enzyme tolerance, allowing for complete pre-mixing of reaction reagents.
RT-PCR, HS PCR
HS17001
Hot start Taq V3
Enzyme
Antibody-modified enzyme, rapid heat activation at 95°C for 30 seconds.
RT-PCR, HS PCR
HS17006
Hot start Tag V4
Enzyme
1) Antibody-modified enzyme, rapid heat activation at 95℃ for 30 seconds. 2) Fast amplification speed, suitable for molecular POCT platforms. 3) Has certain anti-interference capability.
RT-PCR, HS PCR
HS194
MMLV Reverse Transcriptase
Enzyme
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RT-PCR, HS PCR
HS195
SuperI Reverse Transcriptase
Enzyme
1) Good thermal stability, can withstand reaction temperatures up to 60°C. 2) Verified through long-term stability and thermal acceleration experiments, with no significant decrease in activity after 7 days at 37°C.
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HS18
Uracil DNA Glycosylase
Enzym
Anti-pollution amplification, rapid inactivation at 95°C for 10 minutes.
RT-PCR, HS PCR
HS24-02
Taq-HS qPCR Mix (No Rox)
Blend
Hot start (chemical modification), multiple rapid, without ROX.
RT-PCR, HS PCR
HS231
Taq antibody II
Ab
Multi-table blocking is better for inhibiting the exonuclease activity of Taq enzyme, and it is used in conjunction with Taq polymerase.
RT-PCR, HS PCR
HS23-1
Taq antibody III
Ab
No nuclease residue, no nucleic acid residue, multi-epitope blocking, used in conjunction with Taq polymerase.
