Rapid Plus DNA Lib Prep Kit V2 (No DDREs)

$352.59

Rapid Plus DNA Lib Prep Kit V2 (No DDREs) (Cat. NO RK20271) contains the enzymes and buffers required to convert a broad range of input amounts of DNA into high quality libraries for next-generation sequencing on the IlluminaÂ® NGS platforms. Inputs of 1 ng to 1000 ng double-stranded DNA (dsDNA) are required for library preparation. The entire four-step workflow takes place in a single tube or well, in about three hours (Figure 1). No intermediate purification steps or sample transfers are necessary, thus preventing handling errors and loss of valuable samples.
Once purified and quantified, the resulting libraries are ready for Illumina NGS instruments using standard Illumina sequencing reagents and protocols. The kit provides excellent results for high-coverage deep sequencing, such as de novo sequencing, whole genome resequencing, whole exome sequencing, and other enrichment techniques.

Weight	1.00 lbs
Dimensions	5.00 × 5.00 × 5.00 in
Manufacturer	ABclonal Technology
Size/Quantity	1-EA
Product Size	24RXN
Manufacturer Part No	RK20271
Ship to Residential	NO

SKU: Abclonal-RK20271-24RXN

SKU: Abclonal-RK20271-24RXN Category: Antibodies Brand: ABclonal Technology

Description

Description

Size quantity : 1-EA
Description : Rapid Plus DNA Lib Prep Kit V2 (No DDREs) (Cat. NO RK20271) contains the enzymes and buffers required to convert a broad range of input amounts of DNA into high quality libraries for next-generation sequencing on the IlluminaÂ® NGS platforms. Inputs of 1 ng to 1000 ng double-stranded DNA (dsDNA) are required for library preparation. The entire four-step workflow takes place in a single tube or well, in about three hours (Figure 1). No intermediate purification steps or sample transfers are necessary, thus preventing handling errors and loss of valuable samples.
Once purified and quantified, the resulting libraries are ready for Illumina NGS instruments using standard Illumina sequencing reagents and protocols. The kit provides excellent results for high-coverage deep sequencing, such as de novo sequencing, whole genome resequencing, whole exome sequencing, and other enrichment techniques.

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