Dry Ice

PowerPol 2X PCR Mix with Dye V2 is an optimized premix with amplification rates up to 10 s/kb to save PCR reaction time. Reagents include DNA polymerases, dNTPs, MgCl2, KCI, and other stabilizers. It only needs to add primers and templates to perform amplification. This product contains loading buffer, PCR products can be directly loaded for electrophoresis.
PowerPol 2X PCR Mix with Dye V2 can use complex genomic DNA as a template to amplify a 5 kb target fragment or a simple template such as lambda DNA to amplify a 10 kb target fragment. It is suitable for colony PCR, genotype identification, vector construction, and other applications.

PowerPol 2X PCR Mix with Dye V2 is an optimized premix with amplification rates up to 10 s/kb to save PCR reaction time. Reagents include DNA polymerases, dNTPs, MgCl2, KCI, and other stabilizers. It only needs to add primers and templates to perform amplification. This product contains loading buffer, PCR products can be directly loaded for electrophoresis.
PowerPol 2X PCR Mix with Dye V2 can use complex genomic DNA as a template to amplify a 5 kb target fragment or a simple template such as lambda DNA to amplify a 10 kb target fragment. It is suitable for colony PCR, genotype identification, vector construction, and other applications.

PowerPol 2X PCR Mix with Dye V2 is an optimized premix with amplification rates up to 10 s/kb to save PCR reaction time. Reagents include DNA polymerases, dNTPs, MgCl2, KCI, and other stabilizers. It only needs to add primers and templates to perform amplification. This product contains loading buffer, PCR products can be directly loaded for electrophoresis.
PowerPol 2X PCR Mix with Dye V2 can use complex genomic DNA as a template to amplify a 5 kb target fragment or a simple template such as lambda DNA to amplify a 10 kb target fragment. It is suitable for colony PCR, genotype identification, vector construction, and other applications.

Powerpol HS 2X PCR Mix for Mouse Genotyping is one of kit components of Mouse Tissue Direct PCR Kit (ABclonal RK20736), which was used for extra needs when user are dealing with multi-primer amplification and consuming such mix in a volume larger than a regular kit size form.
Powerpol HS 2X PCR Mix for Mouse Genotyping only needs to add primers and templates to perform amplification, and the reagent contains loading buffer, PCR products can be directly loaded for electrophoresis.

Powerpol HS 2X PCR Mix for Mouse Genotyping is one of kit components of Mouse Tissue Direct PCR Kit (ABclonal RK20736), which was used for extra needs when user are dealing with multi-primer amplification and consuming such mix in a volume larger than a regular kit size form.
Powerpol HS 2X PCR Mix for Mouse Genotyping only needs to add primers and templates to perform amplification, and the reagent contains loading buffer, PCR products can be directly loaded for electrophoresis.

Proteinase K

5’…C T G C A/ G…3′
3’…G/ A C G T C…5′
Isoschizomers: BspMAI

5’…C A G/ C T G…3′
3’…G T C/ G A C…5′

The Rapid Plus DNA Lib Prep kit provides a streamlined and efficient method to construction DNA library for next generation sequencing (NGS) at Illumina® platforms. The entire protocol can be completed in 2 hours. Starting from fragmented input-DNA (1 – 1000 ng), the kit contains all the enzymes and buffers for end-preparation, adapter ligation and library amplification. To simplify the workflow, the fragmented DNA is end-repaired and adenylated during the initial step. The kit can be conveniently used for construction of PCR-free library from 100 ng of high-quality fragmented genomic DNA, or 10 ng of circulating cell-free DNA (cfDNA). PCR primers provided in the kit are optional for users who prefer self-selected high-fidelity DNA polymerases in the library amplification.
The kit also provides DNA repair enzymes, which could repair DNA damages such as nicks, gaps, oxidized bases, damaged/blocked 3’ ends, AP sites (apurinic/apyrimidinic sites), and uracil bases. In addition, the DNA repair enzymes significantly increase the NGS library yields from FFPE-derived DNA.

The Rapid Plus DNA Lib Prep kit provides a streamlined and efficient method to construction DNA library for next generation sequencing (NGS) at Illumina® platforms. The entire protocol can be completed in 2 hours. Starting from fragmented input-DNA (1 – 1000 ng), the kit contains all the enzymes and buffers for end-preparation, adapter ligation and library amplification. To simplify the workflow, the fragmented DNA is end-repaired and adenylated during the initial step. The kit can be conveniently used for construction of PCR-free library from 100 ng of high-quality fragmented genomic DNA, or 10 ng of circulating cell-free DNA (cfDNA). PCR primers provided in the kit are optional for users who prefer self-selected high-fidelity DNA polymerases in the library amplification.
The kit also provides DNA repair enzymes, which could repair DNA damages such as nicks, gaps, oxidized bases, damaged/blocked 3’ ends, AP sites (apurinic/apyrimidinic sites), and uracil bases. In addition, the DNA repair enzymes significantly increase the NGS library yields from FFPE-derived DNA.

The Rapid Plus DNA Lib Prep kit for Illumina® V2 provides a streamlined and efficient method to construct DNA libraries for next generation sequencing (NGS) on Illumina® sequencing platforms. This kit is an updated version of the original Rapid Plus DNA Lib Prep kit (Cat. Nos. RK20208) that has been further optimized to provide superior DNA damage repair and improve ligation efficiency with low-input DNA. The entire protocol can be completed within 2 hours. Starting from fragmented input-DNA (1 – 1000 ng), the kit contains all of the necessary enzymes and buffers for end-preparation, adapter ligation and library amplification. To simplify the workflow, fragmented DNA is end-repaired and adenylated during one initial step. The kit can be conveniently used for construction of PCR-free libraries beginning with 100 ng of high-quality fragmented genomic DNA, or from 10 ng of circulating cell-free DNA (cfDNA). PCR primers provided in the kit are optional for users who prefer self-selected high-fidelity DNA polymerases in library amplification.The kit also provides DNA repair enzymes which repair DNA damage such as nicks, gaps, oxidized bases, damaged/blocked 3’ ends, AP sites (apurinic/apyrimidinic sites), and uracil bases. In addition, the DNA repair enzymes significantly increase NGS library yields from FFPE-derived DNA.

The Rapid Plus DNA Lib Prep kit for Illumina® V2 provides a streamlined and efficient method to construct DNA libraries for next generation sequencing (NGS) on Illumina® sequencing platforms. This kit is an updated version of the original Rapid Plus DNA Lib Prep kit (Cat. Nos. RK20208) that has been further optimized to provide superior DNA damage repair and improve ligation efficiency with low-input DNA. The entire protocol can be completed within 2 hours. Starting from fragmented input-DNA (1 – 1000 ng), the kit contains all of the necessary enzymes and buffers for end-preparation, adapter ligation and library amplification. To simplify the workflow, fragmented DNA is end-repaired and adenylated during one initial step. The kit can be conveniently used for construction of PCR-free libraries beginning with 100 ng of high-quality fragmented genomic DNA, or from 10 ng of circulating cell-free DNA (cfDNA). PCR primers provided in the kit are optional for users who prefer self-selected high-fidelity DNA polymerases in library amplification.The kit also provides DNA repair enzymes which repair DNA damage such as nicks, gaps, oxidized bases, damaged/blocked 3’ ends, AP sites (apurinic/apyrimidinic sites), and uracil bases. In addition, the DNA repair enzymes significantly increase NGS library yields from FFPE-derived DNA.

The Rapid Plus DNA Lib Prep kit for Illumina® V2 provides a streamlined and efficient method to construct DNA libraries for next generation sequencing (NGS) on Illumina® sequencing platforms. This kit is an updated version of the original Rapid Plus DNA Lib Prep kit (Cat. Nos. RK20208) that has been further optimized to provide superior DNA damage repair and improve ligation efficiency with low-input DNA. The entire protocol can be completed within 2 hours. Starting from fragmented input-DNA (1 – 1000 ng), the kit contains all of the necessary enzymes and buffers for end-preparation, adapter ligation and library amplification. To simplify the workflow, fragmented DNA is end-repaired and adenylated during one initial step. The kit can be conveniently used for construction of PCR-free libraries beginning with 100 ng of high-quality fragmented genomic DNA, or from 10 ng of circulating cell-free DNA (cfDNA). PCR primers provided in the kit are optional for users who prefer self-selected high-fidelity DNA polymerases in library amplification.The kit also provides DNA repair enzymes which repair DNA damage such as nicks, gaps, oxidized bases, damaged/blocked 3’ ends, AP sites (apurinic/apyrimidinic sites), and uracil bases. In addition, the DNA repair enzymes significantly increase NGS library yields from FFPE-derived DNA.

Rapid Plus DNA Lib Prep Kit for MGI V2

Rapid Plus DNA Lib Prep Kit for MGI V2

Rapid Plus DNA Lib Prep Kit for MGI V2