Dry Ice

ABclonal First Strand Synthesis Module (RK20353) is designed for RNA fragmentation and first strand cDNA synthesis in RNA-seq library construction. The second strand cDNA can be directly synthesized without purifying the first strand cDNA product. The RT Reagent in this module does not contain Actinomycin D and can be used with ABclonal Second Strand Synthesis Module (RK20346) to make RNA libraries. In addition, Frag/Elute Buffer employs Mg²⁺ at high temperature conditions to fragment the RNA. Therefore, the RNA sample cannot contain metal ions such as Mg²⁺ or a metal ion chelating agent such as EDTA, which may affect the fragmentation size of RNA.

ABclonal First Strand Synthesis Module (RK20353) is designed for RNA fragmentation and first strand cDNA synthesis in RNA-seq library construction. The second strand cDNA can be directly synthesized without purifying the first strand cDNA product. The RT Reagent in this module does not contain Actinomycin D and can be used with ABclonal Second Strand Synthesis Module (RK20346) to make RNA libraries. In addition, Frag/Elute Buffer employs Mg²⁺ at high temperature conditions to fragment the RNA. Therefore, the RNA sample cannot contain metal ions such as Mg²⁺ or a metal ion chelating agent such as EDTA, which may affect the fragmentation size of RNA.

First Strand Synthesis Module (Stranded)

First Strand Synthesis Module (Stranded)

FS Module

The FS Pro DNA Lib Prep Kit for Illumina is designed for DNA library preparation for next generation sequencing (NGS) on Illumina® platforms. This kit integrates DNA fragmentation with end repair and dA tailing into one step, and it can be directly followed by adapter ligation without purification. With greatly simplified experimental flow, the entire experiment can be completed within 2 hours. This kit is compatible with DNA samples from different species and different origins. Optimization of reagents and protocol greatly reduced rates of false positives, significantly improving sequencing yield and overall results, including with FFPE DNA samples. This kit is suitable for the construction of PCR-Free libraries (e.g., 100 ng of high-quality genomic DNA).
The components of the kit have undergone strict quality control, mainly including component pollution test, functional test verification, application scenario test and product batch stability test, etc., to minimize the residue of pathogenic bacteria and apply to the detection of pathogenic bacteria.

The FS Pro DNA Lib Prep Kit for Illumina is designed for DNA library preparation for next generation sequencing (NGS) on Illumina® platforms. This kit integrates DNA fragmentation with end repair and dA tailing into one step, and it can be directly followed by adapter ligation without purification. With greatly simplified experimental flow, the entire experiment can be completed within 2 hours. This kit is compatible with DNA samples from different species and different origins. Optimization of reagents and protocol greatly reduced rates of false positives, significantly improving sequencing yield and overall results, including with FFPE DNA samples. This kit is suitable for the construction of PCR-Free libraries (e.g., 100 ng of high-quality genomic DNA).
The components of the kit have undergone strict quality control, mainly including component pollution test, functional test verification, application scenario test and product batch stability test, etc., to minimize the residue of pathogenic bacteria and apply to the detection of pathogenic bacteria.

The FS Pro DNA Lib Prep Kit V2 is designed for DNA library preparation for next generation sequencing (NGS) on Illumina® platforms. This kit integrates DNA fragmentation with end repair and dA tailing into one step, and it can be directly followed by adapter ligation without purification. With greatly simplified experimental flow, the entire experiment can be completed within 2 hours. This kit is compatible with DNA samples from different species and different origins. Optimization of reagents and protocol greatly reduced rates of false positives, significantly improving sequencing yield and overall results, including with FFPE DNA samples. This kit is suitable for the construction of PCR-Free libraries (e.g., 100 ng of high-quality genomic DNA).
The components of the kit have undergone strict quality control, mainly including component pollution test, functional test verification, application scenario test and product batch stability test, etc., to minimize the residue of pathogenic bacteria and apply to the detection of pathogenic bacteria.

The FS Pro DNA Lib Prep Kit V2 is designed for DNA library preparation for next generation sequencing (NGS) on Illumina® platforms. This kit integrates DNA fragmentation with end repair and dA tailing into one step, and it can be directly followed by adapter ligation without purification. With greatly simplified experimental flow, the entire experiment can be completed within 2 hours. This kit is compatible with DNA samples from different species and different origins. Optimization of reagents and protocol greatly reduced rates of false positives, significantly improving sequencing yield and overall results, including with FFPE DNA samples. This kit is suitable for the construction of PCR-Free libraries (e.g., 100 ng of high-quality genomic DNA).
The components of the kit have undergone strict quality control, mainly including component pollution test, functional test verification, application scenario test and product batch stability test, etc., to minimize the residue of pathogenic bacteria and apply to the detection of pathogenic bacteria.

Real-time Quantitative PCR (qPCR) is a powerful technique in detecting initial DNA input in a PCR reaction by fluorescence signal accumulation. ABclonal Genious 2X SYBR Green Fast qPCR Mix is a fluorescence reagent for qPCR reactions using the SYBR® Green I. This product provides real-time data on DNA amplification during PCR by performing quantitative fluorescence signal detection on SYBR® / FAM channels. This product uses the antibody-based hot-start Taq enzyme for amplification, which greatly improves the specificity of the product while ensuring the amplification effect. At the same time, by optimizing the qPCR Mix Buffer system, the product is suitable for multiple species, providing a powerful tool for multidisciplinary experimental needs.
This product is a 2X pre-mix enzyme, contains all the components required for qPCR except primers and templates, providing great convenience for experimental manipulation.

Real-time Quantitative PCR (qPCR) is a powerful technique in detecting initial DNA input in a PCR reaction by fluorescence signal accumulation. ABclonal Genious 2X SYBR Green Fast qPCR Mix is a fluorescence reagent for qPCR reactions using the SYBR® Green I. This product provides real-time data on DNA amplification during PCR by performing quantitative fluorescence signal detection on SYBR® / FAM channels. This product uses the antibody-based hot-start Taq enzyme for amplification, which greatly improves the specificity of the product while ensuring the amplification effect. At the same time, by optimizing the qPCR Mix Buffer system, the product is suitable for multiple species, providing a powerful tool for multidisciplinary experimental needs.
This product is a 2X pre-mix enzyme, contains all the components required for qPCR except primers and templates, providing great convenience for experimental manipulation.

Real-time Quantitative PCR (qPCR) is a powerful technique in detecting initial DNA input in a PCR reaction by fluorescence signal accumulation. ABclonal Genious 2X SYBR Green Fast qPCR Mix is a fluorescence reagent for qPCR reactions using the SYBR® Green I. This product provides real-time data on DNA amplification during PCR by performing quantitative fluorescence signal detection on SYBR® / FAM channels. This product uses the antibody-based hot-start Taq enzyme for amplification, which greatly improves the specificity of the product while ensuring the amplification effect. At the same time, by optimizing the qPCR Mix Buffer system, the product is suitable for multiple species, providing a powerful tool for multidisciplinary experimental needs.
This product is a 2X pre-mix enzyme, contains all the components required for qPCR except primers and templates, providing great convenience for experimental manipulation.

Real-time Quantitative PCR (qPCR) is a powerful technique in detecting initial DNA input in a PCR reaction by fluorescence signal accumulation. The DNA double strand bonded dye, SYBR® Green I, is the most commonly used dye in qPCR. ABclonal Genious 2X SYBR Green Fast qPCR Mix (High ROX Premixed) is an optimized SYBR Green qPCR reaction mix which can used in machines with High ROX mode, It contains all required components in qPCR except primers and template. It is convenient for experiment and suitable for multiple species. The above features make it as an ideal experiment tool for gene quantitative research.

Real-time Quantitative PCR (qPCR) is a powerful technique in detecting initial DNA input in a PCR reaction by fluorescence signal accumulation. The DNA double strand bonded dye, SYBR® Green I, is the most commonly used dye in qPCR. ABclonal Genious 2X SYBR Green Fast qPCR Mix (High ROX Premixed) is an optimized SYBR Green qPCR reaction mix which can used in machines with High ROX mode, It contains all required components in qPCR except primers and template. It is convenient for experiment and suitable for multiple species. The above features make it as an ideal experiment tool for gene quantitative research.

Real-time Quantitative PCR (qPCR) is a powerful technique in detecting initial DNA input in a PCR reaction by fluorescence signal accumulation. The DNA double strand bonded dye, SYBR® Green I, is the most commonly used dye in qPCR. ABclonal Genious 2X SYBR Green Fast qPCR Mix (High ROX Premixed) is an optimized SYBR Green qPCR reaction mix which can used in machines with High ROX mode, It contains all required components in qPCR except primers and template. It is convenient for experiment and suitable for multiple species. The above features make it as an ideal experiment tool for gene quantitative research.

Real-time Quantitative PCR (qPCR) is a powerful technique in detecting initial DNA input in a PCR reaction by fluorescence signal accumulation. The DNA double strand bonded dye, SYBR® Green I, is the most commonly used dye in qPCR. ABclonal Genious 2X SYBR Green Fast qPCR Mix (Low ROX) is an optimized SYBR Green qPCR reaction mix which can used in machines with Low ROX mode, It contains all required components in qPCR except primers and template. It is convenient for experiment and suitable for multiple species. The above features make it as an ideal experiment tool for gene quantitative research.

Real-time Quantitative PCR (qPCR) is a powerful technique in detecting initial DNA input in a PCR reaction by fluorescence signal accumulation. The DNA double strand bonded dye, SYBR® Green I, is the most commonly used dye in qPCR. ABclonal Genious 2X SYBR Green Fast qPCR Mix (Low ROX) is an optimized SYBR Green qPCR reaction mix which can used in machines with Low ROX mode, It contains all required components in qPCR except primers and template. It is convenient for experiment and suitable for multiple species. The above features make it as an ideal experiment tool for gene quantitative research.

Real-time Quantitative PCR (qPCR) is a powerful technique in detecting initial DNA input in a PCR reaction by fluorescence signal accumulation. The DNA double strand bonded dye, SYBR® Green I, is the most commonly used dye in qPCR. ABclonal Genious 2X SYBR Green Fast qPCR Mix (Low ROX) is an optimized SYBR Green qPCR reaction mix which can used in machines with Low ROX mode, It contains all required components in qPCR except primers and template. It is convenient for experiment and suitable for multiple species. The above features make it as an ideal experiment tool for gene quantitative research.

Real-time Quantitative PCR (qPCR) is a powerful techniqueindetectinginitial DNA inputina PCR reaction by fluorescence signal accumulation. The DNA double strand bonded dye, SYBR® Green I is the most commonly used dye in qPCR. ABclonal Genious 2X SYBR Green Fast qPCR Mix (No ROX) is an optimized SYBR Green qPCR reaction mix which can used in machines with no ROX mode, It contains all required components in qPCR except primers and template. It is convenient for experiment and suitable for multiple species. The above features make it as an ideal experiment tool for gene quantitative research.

Real-time Quantitative PCR (qPCR) is a powerful techniqueindetectinginitial DNA inputina PCR reaction by fluorescence signal accumulation. The DNA double strand bonded dye, SYBR® Green I is the most commonly used dye in qPCR. ABclonal Genious 2X SYBR Green Fast qPCR Mix (No ROX) is an optimized SYBR Green qPCR reaction mix which can used in machines with no ROX mode, It contains all required components in qPCR except primers and template. It is convenient for experiment and suitable for multiple species. The above features make it as an ideal experiment tool for gene quantitative research.

Real-time Quantitative PCR (qPCR) is a powerful techniqueindetectinginitial DNA inputina PCR reaction by fluorescence signal accumulation. The DNA double strand bonded dye, SYBR® Green I is the most commonly used dye in qPCR. ABclonal Genious 2X SYBR Green Fast qPCR Mix (No ROX) is an optimized SYBR Green qPCR reaction mix which can used in machines with no ROX mode, It contains all required components in qPCR except primers and template. It is convenient for experiment and suitable for multiple species. The above features make it as an ideal experiment tool for gene quantitative research.

Gloria Nova HS DNA polymerase is an ideal enzyme for high fidelity PCR with excellent processivity. It is a novel engineered enzyme with unique structure. Gloria Nova HS DNA polymerase contains a recombinant synthetic enhanced domain to increase fidelity and extension speed. The antibody-mediated hot-start feature significantly inhibits non-specific amplifications at room temperature. Gloria Nova is one of the thermostable DNA polymerases with strong 3 ’-5 ’ exonuclease activity (proofreading activity), which results in its extreme high fidelity.The Gloria Nova HS 2X Master Mix is an ideal product with good amplification efficiency for diversity templates including animals, plants, cDNA, etc.

Gloria Nova HS DNA polymerase is an ideal enzyme for high fidelity PCR with excellent processivity. It is a novel engineered enzyme with unique structure. Gloria Nova HS DNA polymerase contains a recombinant synthetic enhanced domain to increase fidelity and extension speed. The antibody-mediated hot-start feature significantly inhibits non-specific amplifications at room temperature. Gloria Nova is one of the thermostable DNA polymerases with strong 3 ’-5 ’ exonuclease activity (proofreading activity), which results in its extreme high fidelity.The Gloria Nova HS 2X Master Mix is an ideal product with good amplification efficiency for diversity templates including animals, plants, cDNA, etc.

This product utilizes antibody-blocked high-fidelity DNA polymerase, enabling high-specificity hot-start PCR. It has approximately 120× the fidelity of Taq polymerase, making it ideal for molecular cloning and effective for various templates such as animal, plant, and cDNA samples.

This product utilizes antibody-blocked high-fidelity DNA polymerase, enabling high-specificity hot-start PCR. It has approximately 120× the fidelity of Taq polymerase, making it ideal for molecular cloning and effective for various templates such as animal, plant, and cDNA samples.

Gloria Nova HS DNA polymerase is an ideal enzyme for high fidelity PCR with excellent processivity. It is a novel engineered enzyme with unique structure. Gloria Nova HS DNA polymerase contains a recombinant synthetic enhanced domain to increase fidelity and extension speed. The antibody-mediated hot-start feature significantly inhibits non-specific amplifications at room temperature. Gloria Nova is one of the thermostable DNA polymerases with strong 3 ’-5 ’ exonuclease activity (proofreading activity), which results in its extreme high fidelity.The Gloria Nova HS 2X Master Mix is an ideal product with good amplification efficiency for diversity templates including animals, plants, cDNA, etc.

Gloria Nova HS DNA polymerase is an ideal enzyme for high fidelity PCR with excellent processivity. It is a novel engineered enzyme with unique structure. Gloria Nova HS DNA polymerase contains a recombinant synthetic enhanced domain to increase fidelity and extension speed. The antibody-mediated hot-start feature significantly inhibits non-specific amplifications at room temperature. Gloria Nova is one of the thermostable DNA polymerases with strong 3 ’-5 ’ exonuclease activity (proofreading activity), which results in its extreme high fidelity.The Gloria Nova HS 2X Master Mix is an ideal product with good amplification efficiency for diversity templates including animals, plants, cDNA, etc.

This product utilizes antibody-blocked high-fidelity DNA polymerase, enabling high-specificity hot-start PCR. It has approximately 120× the fidelity of Taq polymerase, making it ideal for molecular cloning and effective for various templates such as animal, plant, and cDNA samples.

This product utilizes antibody-blocked high-fidelity DNA polymerase, enabling high-specificity hot-start PCR. It has approximately 120× the fidelity of Taq polymerase, making it ideal for molecular cloning and effective for various templates such as animal, plant, and cDNA samples.

Gloria Nova HS DNA polymerase is a typical B-family polymerase with a unique structure. It is a new enzyme similar to Pyrococcus furiosus, fused with a continuous synthesis enhancement domain, which improves elongation, yield and specificity.
Gloria Nova HS DNA polymerase is equipped with specific antibodies, which effectively inhibits non-specific amplification and improves the stability of Gloria Nova HS DNA polymerase.
Gloria Nova HS DNA polymerase has 5′-3′ continuous synthesis activity and 3′-5′ exonuclease activity, and its amplified products are blunt-ended.
Gloria Nova DNA polymerase is a mutant polymerase modified by genetic engineering. It has the ability to incorporate dUTP and can also amplify complex templates with dU.
Gloria Nova HS 2X PCR Mix for NGS is an easy-to-operate 2X Mix, which contains Gloria Nova HS DNA polymerase, buffer, Mg⁺ and dNTPs, etc. Only additional DNA template, primers and water are needed in the amplification system. Perform amplification.
All batches of Gloria Nova HS 2X PCR Mix for NGS have undergone strict quality control to ensure the stable performance of each batch of reagents.

Gloria Nova HS DNA polymerase is a typical B-family polymerase with a unique structure. It is a new enzyme similar to Pyrococcus furiosus, fused with a continuous synthesis enhancement domain, which improves elongation, yield and specificity.
Gloria Nova HS DNA polymerase is equipped with specific antibodies, which effectively inhibits non-specific amplification and improves the stability of Gloria Nova HS DNA polymerase.
Gloria Nova HS DNA polymerase has 5′-3′ continuous synthesis activity and 3′-5′ exonuclease activity, and its amplified products are blunt-ended.
Gloria Nova DNA polymerase is a mutant polymerase modified by genetic engineering. It has the ability to incorporate dUTP and can also amplify complex templates with dU.
Gloria Nova HS 2X PCR Mix for NGS is an easy-to-operate 2X Mix, which contains Gloria Nova HS DNA polymerase, buffer, Mg⁺ and dNTPs, etc. Only additional DNA template, primers and water are needed in the amplification system. Perform amplification.
All batches of Gloria Nova HS 2X PCR Mix for NGS have undergone strict quality control to ensure the stable performance of each batch of reagents.

Gloria Nova HS DNA polymerase is an ideal enzyme for high fidelity PCR with excellent processivity. It is a novel engineered enzyme with comparable performance to Pyrococcus furiosus DNA polymerase.
With unique structure Gloria Nova HS DNA polymerase contains a recombinant synthesis enhancement domain to increase fidelity and extension speed. The antibody-mediated hot-start feature significantly inhibits non-specific amplifications at room temperature.
Gloria Nova is one of the thermostable DNA polymerases with strong 3’-5’ exonuclease activity (proofreading activity), which results in its extreme high fidelity, 10-15 times higher than Taq DNA polymerase and 6 times higher than Pyrococcus furiosus DNA polymerase.
The Gloria Nova HS PCR Kit is supplied with a 5X Gloria Nova HF Buffer and a 2.5X Gloria Nova GC Buffer. The 5X Gloria Nova HF Buffer is an optimized buffer for general high fidelity amplifications while the 2.5X Gloria Nova GC Buffer is used in the amplifications of problematic or GC-rich templates.