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RT-PCR Easyᵀᴹ I(One Step)
◮ The one-step kit enables reverse transcription and PCR to be carried out in the same tube. It only needs to add template RNA, specific PCR primers and RNase-Free ddH2O.
◮ Real-time quantitative analysis of RNA can be carried out quickly and accurately.
◮ The kit uses a unique Foregene reverse transcription reagent and Foregene HotStar Taq DNA Polymerase combined with a unique reaction system to effectively improve the amplification efficiency and specificity of the reaction.
◮ The optimized reaction system makes the reaction have higher detection sensitivity, stronger thermal stability, and better tolerance.
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Mouse Tail DNA Mini Kit Genomic DNA Extraction Kits from Mouse Tail
The world’s fastest kit for extracting mouse tail genomic DNA, which can extract high-quality genomic DNA from mouse tail within 1 hour.
◮ No RNase contamination: The DNA-Only Column provided by the kit makes it possible to remove the RNA from the genomic DNA without adding RNase during the experiment, preventing the laboratory from being contaminated by exogenous RNase.
◮ Fast speed: Foregene Protease has higher activity than similar proteases, and digests tissue samples quickly; the operation is simple, and the genomic DNA extraction operation can be completed within 20-80 minutes.
◮ Convenient: The centrifugation is performed at room temperature, and there is no need for 4°C low-temperature centrifugation or ethanol precipitation of DNA.
◮ Safety: No organic reagent extraction is required.
◮ High quality: The extracted genomic DNA has large fragments, no RNA, no RNase, and extremely low ion content, which can meet the requirements of various experiments.
◮ Micro-elution system: It can increase the concentration of genomic DNA, which is convenient for downstream detection or experiment.
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Bacterial DNA Isolation Kit Bacterial Genomic DNA Extraction Purification Kits
Quickly purify high-quality genomic DNA from bacteria in the logarithmic growth phase.
◮ No RNase contamination: The DNA-Only Column provided by the kit makes it possible to remove the RNA from the genomic DNA without adding RNase during the experiment, preventing the laboratory from being contaminated by exogenous RNase.
◮ Fast speed: Foregene Protease has higher activity than similar proteases, and digests tissue samples quickly; the operation is simple, and the genomic DNA extraction operation can be completed within 20-80 minutes.
◮ Convenient: The centrifugation is performed at room temperature, and there is no need for 4°C low-temperature centrifugation or ethanol precipitation of DNA.
◮ Safety: No organic reagent extraction is required.
◮ High quality: The extracted genomic DNA has large fragments, no RNA, no RNase, and extremely low ion content, which can meet the requirements of various experiments.
◮ Micro-elution system: It can increase the concentration of genomic DNA, which is convenient for downstream detection or experiment.
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ERG1/TERT Dual Color Probe
Fluorescence in situ hybridization (FISH) is based on the principle of complementary pairing of DNA bases, and the visualization of hybridization signals of fluorescence-labeled DNA probes with its DNA target sequences in cell nucleus under fluorescence microscope.
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DNA/RNA Extraction Kit (Magnetic Beads)
- The whole isolation process is safe and convenient
- The extracted cell free DNA has high yield, high purity and reliable quality
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20q12/20q13.33 Dual Color Probe
According to the principle of complementary pairing of DNA bases, 20q12 (D20S108) orange probe and 20q33.3 green probe were used to hybridize with the DNA target sequence in the nucleus, and the gene state information in the nucleus was observed and analyzed under fluorescence microscope.
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p53/D13S319 Dual Color Probe
Fluorescence in situ hybridization (FISH) is based on the principle of complementary pairing of DNA bases, and the visualization of hybridization signals of fluorescence-labeled DNA probes with its DNA target sequences in cell nucleus under fluorescence microscope.
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EndoFree Maxi Plasmid Kit (Spin Column)
The whole extraction process takes only 1 hour, ensuring the convenient and quick operation.
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MALT1 Dual Color Break Apart probe
According to the principle of DNA base complementary pairing, MALT1 orange-red probe and MALT1 green probe were used to hybridize with the DNA target sequence in the nucleus, and the gene state information in the nucleus was observed and analyzed under a fluorescence microscope.
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D7S522/CSP7 Dual Color Probe
Fluorescence in situ hybridization (FISH) is based on the principle of complementary pairing of DNA bases, and the visualization of hybridization signals of fluorescence-labeled DNA probes with its DNA target sequences in cell nucleus under fluorescence microscope.
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DAPI Counterstain
The main component of DAPI re-staining solution is 4-phenylindole, which can penetrate the cell membrane and bind strongly to DNA.
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BCR ABL1 Dual Color Dual Fusion Probe
According to the principle of DNA base complementary pairing, ABL orange-red probe and BCR green probe were used to hybridize with the DNA target sequence in the nucleus, and the gene state information in the nucleus was observed and analyzed under a fluorescence microscope.
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