Dry Ice

The 100 bp DNA Ladder is a ready-to-use DNA Ladder, which is pre-mixed with loading dye for direct gelloading. This product consists of 11 individual DNA fragments: 100 bp, 200 bp, 300 bp, 400 bp, 500 bp, 600 bp, 700 bp, 800 bp, 900 bp, 1000 bp and 1500 bp, derived from amixture of PCR products and specifically digested plasmid DNA. The 500 bp fragment is present at increased intensity for easy identification.

The 100 bp DNA Ladder is a ready-to-use DNA Ladder, which is pre-mixed with loading dye for direct gelloading. This product consists of 11 individual DNA fragments: 100 bp, 200 bp, 300 bp, 400 bp, 500 bp, 600 bp, 700 bp, 800 bp, 900 bp, 1000 bp and 1500 bp, derived from amixture of PCR products and specifically digested plasmid DNA. The 500 bp fragment is present at increased intensity for easy identification.

10X ILM PCR Primers

10X ILM PCR Primers

10X MGI UDI Primers

10X MGI UDI Primers

2X FASA™ Genotyping Master Mix (Standard ROX)

2X FASA™ Genotyping Master Mix (Standard ROX)

2X MultiF Seamless Assembly Mix

2X MultiF Seamless Assembly Mix

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 2X Universal SYBR Green Fast qPCR Mix contains de novel designed universal reference dye, which can realize higher signal resolution and suits for all currently used qPCR instruments (including high ROX mode, low ROX mode and No ROX mode required machines). It also contains Hot-Start Taq DNA polymerase to avoid unexpected amplification results.
Besides, ABclonal 2X Universal SYBR Green Fast qPCR Mix is an optimized qPCR reaction mix, 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 2X Universal SYBR Green Fast qPCR Mix contains de novel designed universal reference dye, which can realize higher signal resolution and suits for all currently used qPCR instruments (including high ROX mode, low ROX mode and No ROX mode required machines). It also contains Hot-Start Taq DNA polymerase to avoid unexpected amplification results.
Besides, ABclonal 2X Universal SYBR Green Fast qPCR Mix is an optimized qPCR reaction mix, 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.

The 5′ Deadenylase derived from yeast can remove adenosine residues from the 5′-end of DNA and RNA, retaining the 5′-end phosphate group. It can cleave AppppA to produce ATP and AMP.

5’App-T4 DNA Ligase is a mutant of T4 DNA Ligase without adenylation function, which can specifically ligates the pre-adenylated 5´ end of DNA or RNA to the 3´ end of DNA. This enzyme does not require ATP as a cofactor for ligation, but requires a pre-adenylated substrate. This enzyme reduces background ligation (chimera formation) during NGS library construction, because it can only use 5 ‘preadenylation adapter to the DNA fragments.

5’App-T4 DNA Ligase is a mutant of T4 DNA Ligase without adenylation function, which can specifically ligates the pre-adenylated 5´ end of DNA or RNA to the 3´ end of DNA. This enzyme does not require ATP as a cofactor for ligation, but requires a pre-adenylated substrate. This enzyme reduces background ligation (chimera formation) during NGS library construction, because it can only use 5 ‘preadenylation adapter to the DNA fragments.

6X DNA/RNA loading Buffer

Recombinase polymerase amplification (RPA) is a novel nucleic acid amplification technique (NAAT) that enables rapid amplification of targets at a constant low temperature (37~42°C); The target nucleic acid molecules can be amplified to detectable levels within 10-30 minutes. This kit helps user acheive high detection sensitivity, specificity, and short reaction time (only 15-25 minutes). The reaction components are in the form of lyophilized beads, which are easy to operate and store. This reagent can be used for reaction in metal baths, water baths, etc., and user doesn’t need to purchase other expensive devices.

ABclonal Zero TOPO-TA/Blunt Cloning Kit

ABQubit 1X dsDNA HS Assay Kit (Pre-Mixed)

ABQubit 1X dsDNA HS Assay Kit (Pre-Mixed)

ABQubit dsDNA HS Assay Kit

ABQubit dsDNA HS Assay Kit

ABQubit ssDNA Assay Kit

ABQubit ssDNA Assay Kit

ABScript Full Length Reverse Transcriptase for Single Cell

ABScript Full Length Reverse Transcriptase for Single Cell

ABScript GII Reverse Transcriptase is a recombinant Reverse Transcriptase derived from the bacterial group II intron. It exhibits strong thermostability and inhibitor tolerance during RNA Reverse transcription to synthesize cDNA. It is particularly suitable for reverse transcription of RNA samples containing long fragments, complex secondary structures and inhibitory components. ABScript GII Reverse Transcriptase enhances the 5′ end sequencing coverage of long transcripts, making it suitable for RNA-seq applications, such as direct RNA sequencing and long cDNA sequencing.

ABScript GII Reverse Transcriptase is a recombinant Reverse Transcriptase derived from the bacterial group II intron. It exhibits strong thermostability and inhibitor tolerance during RNA Reverse transcription to synthesize cDNA. It is particularly suitable for reverse transcription of RNA samples containing long fragments, complex secondary structures and inhibitory components. ABScript GII Reverse Transcriptase enhances the 5′ end sequencing coverage of long transcripts, making it suitable for RNA-seq applications, such as direct RNA sequencing and long cDNA sequencing.

ABScript HII Reverse Transcriptase is a genetically engineered RNA-dependent DNA polymerase with RNase H activity. The enzyme can use RNA (cDNA synthesis) or ssDNA as a template to synthesize a complementary DNA strand that can be applied to the cDNA synthesis of the first and second strands. This product is compatible with BstL DNA polymerase, especially for RT-LAMP (reverse transcription-loop-mediated isothermal amplification).

ABScript HII Reverse Transcriptase is a genetically engineered RNA-dependent DNA polymerase with RNase H activity. The enzyme can use RNA (cDNA synthesis) or ssDNA as a template to synthesize a complementary DNA strand that can be applied to the cDNA synthesis of the first and second strands. This product is compatible with BstL DNA polymerase, especially for RT-LAMP (reverse transcription-loop-mediated isothermal amplification).