Dry Ice

ABScript Neo RT Master Mix for qPCR with gDNA Remover is an efficient and fast cDNA first-strand synthesis master mix, suitable for two-step RT-qPCR detection. The 4X ABScript Neo RT Mix in this product contains all the reagents required for the reverse transcription reaction. The reaction protocol is simple and can be carried out quickly by adding the RNA template and H₂O. The gDNA Remover Mix in this product can completely remove the genomic DNA remaining in the RNA template and make the qPCR results more accurate. The dsDNase is heat-sensitive and can be quickly and irreversibly inactivated under high temperature conditions. Therefore, it only needs one sample to be used to remove genomic DNA contamination and reverse transcription reactions in the same tube.

5’…G/GTACC…3′
3’…CCATG/G…5′
Isoschizomers: Asp718I

5’…G/GTACC…3′
3’…CCATG/G…5′
Isoschizomers: Asp718I

AFTMag NGS DNA Clean Beads is a SPRI-based chemistry that speeds and simplifies nucleic acid size selection and PCR purification for DNA and/or RNA library preparation for Next Generation sequencing. It is compatible with mainstream NGS library prepared kits. So，it effectively reduce your library preparation costs with the same effect. The protocol can be adapted to your current liquid handling workstation (e.g. Beckman, Hamilton, Tecan, Caliper, Perkin Elmer, Agilent and Eppendorf) utilizing your current protocol as well as it can be performed manually.

AFTMag NGS DNA Clean Beads is a SPRI-based chemistry that speeds and simplifies nucleic acid size selection and PCR purification for DNA and/or RNA library preparation for Next Generation sequencing. It is compatible with mainstream NGS library prepared kits. So，it effectively reduce your library preparation costs with the same effect. The protocol can be adapted to your current liquid handling workstation (e.g. Beckman, Hamilton, Tecan, Caliper, Perkin Elmer, Agilent and Eppendorf) utilizing your current protocol as well as it can be performed manually.

AFTMag Quick Cell-Free DNA Extraction Maxi Kit

AFTMag Quick FFPE DNA Extraction Kit

AFTMag Quick FFPE DNA Extraction Kit

AFTMag Quick FFPE DNA Extraction Kit (Prepackaged)

AFTSpin Blood Fast RNA Extraction Kit

5’…A/CCGGT…3′
3’…TGGCC/A…5′
Isoschizomers: BshTI、AsiGI、CspAI、PinAI

5’…A/CCGGT…3′
3’…TGGCC/A…5′
Isoschizomers: BshTI、AsiGI、CspAI、PinAI

5’…AG/CT…3′
3’…TC/GA…5′

Antarctic Phosphatase (AnP) is a heat-labile alkaline phosphatase purified from a recombinant source. AnP nonspecifically catalyzes the dephosphorylation of 5’and 3’ends of DNA and RNA phosphomonoesters. Also, AnP Hydrolyses ribo-, as well as deoxyribonucleoside triphosphates (NTPs and dNTPs). AnP is completely and irreversibly inactivated by heating at 80°C for 2 minutes, thereby making removal of AnP prior to ligation or end-labeling unnecessary.

Antarctic Phosphatase (AnP) is a heat-labile alkaline phosphatase purified from a recombinant source. AnP nonspecifically catalyzes the dephosphorylation of 5’and 3’ends of DNA and RNA phosphomonoesters. Also, AnP Hydrolyses ribo-, as well as deoxyribonucleoside triphosphates (NTPs and dNTPs). AnP is completely and irreversibly inactivated by heating at 80°C for 2 minutes, thereby making removal of AnP prior to ligation or end-labeling unnecessary.

5’…G/TGCAC…3′
3’…CACGT/G…5′
Isoschizomers: Alw44I、VneI

APOBEC

APOBEC

5’…GG/CGCGCC…3′
3’…CCGCGC/GG…5′
Isoschizomers: SgsI、PalAI

ATAC-Seq Lib Prep Kit for Illumina

5’…C/CTAGG…3′
3’…GGATC/C…5′
Isoschizomers: XmaJI、AspA2I、BlnI

5’…C/CTAGG…3′
3’…GGATC/C…5′
Isoschizomers: XmaJI、AspA2I、BlnI

5’…G/GATCC…3′
3’…CCTAG/G…5′

5’…G/GATCC…3′
3’…CCTAG/G…5′

5’…G A A G A C (N)2 …3′
3’…C T T C T G (N)6 …5′
Isoschizomers: BpiI, BstV2I

5’…GCCNNNN/NGGC…3′
3’…CGGN/NNNNCCG…5′

5’…GCCNNNN/NGGC…3′
3’…CGGN/NNNNCCG…5′

5’…A/ G A T C T…3′
3’…T C T A G/ A…5′

This product is a blue-colored universal SYBR Green reagent, convenient for sampling and using specially designed reference dye (ROX) for higher sensitivity and resolution. It is compatible with all models of fluorescence quantitative PCR instruments (including High ROX, Low ROX, and No ROX required instruments). The reagent introduces a dUTP/UDG system preventing the impact of amplification product contamination on qPCR and ensuring the accuracy of the results. UDG can quickly degrade pollutants containing U at room temperature, and UDG quickly deactivates when pre denatured at 95 ℃, without affecting the efficiency and sensitivity of qPCR. Hot start Taq DNA polymerase is used for amplification, which enhances the specificity of the product. Overall, this product provides a reliable and versatile solution for SYBR Green-based qPCR experiments.