The fundamental principle of DNA library construction involves fragmenting target genomic DNA or cDNA by physical or enzymatic methods, then ligating the fragments to vectors to generate a series of recombinant DNA molecules. The main purpose is to preserve and amplify all or part of the genetic resources of a specific organism for long-term use, enabling subsequent gene screening, sequencing, and functional studies.
Tn5 DNA Library Preparation Kit
- Fast library preparation: less than 90 minutes per sample - Easy operation: single-tube reaction for simultaneous fragmentation and adapter addition - Automation-ready: suitable for high-throughput automated library preparation platforms |
Cat. No. | Description | Packaging |
BL5647A | Tn5 DNA Library Preparation Kit (for Illumina, for 1 ng DNA) | 6 T |
BL5647B | Tn5 DNA Library Preparation Kit (for Illumina, for 1 ng DNA) | 12 T |
BL5647C | Tn5 DNA Library Preparation Kit (for Illumina, for 1 ng DNA) | 24 T |
BL5647D | Tn5 DNA Library Preparation Kit (for Illumina, for 1 ng DNA) | 96 T |
BL5648A | Tn5 DNA Library Preparation Kit (for Illumina, for 50 ng DNA) | 6 T |
BL5648B | Tn5 DNA Library Preparation Kit (for Illumina, for 50 ng DNA) | 12 T |
BL5648C | Tn5 DNA Library Preparation Kit (for Illumina, for 50 ng DNA) | 24 T |
BL5648D | Tn5 DNA Library Preparation Kit (for Illumina, for 50 ng DNA) | 96 T |
DNA Library Preparation Kit
- Simple operation: optimized ligation system reduces pipetting steps - Efficient fragmentation enzyme: minimal bias, high library coverage - Broad sample compatibility: genomic DNA, full-length cDNA, FFPE DNA - Automated library preparation: supports high-throughput automated library construction |
Cat. No. | Description | Packaging |
BL5649A | DNA Library Preparation Kit (for Illumina Platform) | 6 T |
BL5649B | DNA Library Preparation Kit (for Illumina Platform) | 12 T |
BL5649C | DNA Library Preparation Kit (for Illumina Platform) | 24 T |
BL5649D | DNA Library Preparation Kit (for Illumina Platform) | 96 T |
Enzymatic Fragmentation DNA Library Preparation Kit
- Simple operation: fragmentation to adapter ligation completed in a single tube - Efficient fragmentation enzyme: minimal bias, high library coverage - Fewer steps: saves time and reduces bead usage - Broad sample compatibility: genomic DNA, full-length cDNA, FFPE DNA - Automated library preparation: supports high-throughput automated library construction |
Cat. No. | Description | Packaging |
BL5650A | Enzymatic Fragmentation DNA Library Preparation Kit (for Illumina Platform) | 6 T |
BL5650B | Enzymatic Fragmentation DNA Library Preparation Kit (for Illumina Platform) | 12 T |
BL5650C | Enzymatic Fragmentation DNA Library Preparation Kit (for Illumina Platform) | 24 T |
BL5650D | Enzymatic Fragmentation DNA Library Preparation Kit (for Illumina Platform) | 96 T |
DNA Selection Magnetic Beads
DNA Select Beads utilize imported magnetic beads with high binding capacity, fast magnetic response, and low sedimentation based on the Solid Phase Reversible Immobilization (SPRI) principle, combined with an optimized binding buffer. They are designed for nucleic acid purification and fragment size selection, offering high recovery efficiency and purity. The operation method, purification, and size selection performance are highly consistent with Beckman AMPure XP, making them suitable for both manual and automated workflows.
- Efficiently recovers nucleic acid fragments larger than 100 bp - Effectively removes dNTPs, primers, primer dimers, salts, and other impurities - Purifies both double-stranded and single-stranded DNA - Simpler, more efficient, and more economical than traditional column-based purification methods - Compatible with automated workstations for high-throughput sample preparation |
Cat. No. | Description | Packaging |
BL5651A | DNA Selection Magnetic Beads | 5mL |
BL5651B | DNA Selection Magnetic Beads | 60mL |
BL5651C | DNA Selection Magnetic Beads | 450mL |
The fundamental principle of DNA library construction involves fragmenting target genomic DNA or cDNA by physical or enzymatic methods, then ligating the fragments to vectors to generate a series of recombinant DNA molecules. The main purpose is to preserve and amplify all or part of the genetic resources of a specific organism for long-term use, enabling subsequent gene screening, sequencing, and functional studies.
Tn5 DNA Library Preparation Kit
- Fast library preparation: less than 90 minutes per sample - Easy operation: single-tube reaction for simultaneous fragmentation and adapter addition - Automation-ready: suitable for high-throughput automated library preparation platforms |
Cat. No. | Description | Packaging |
BL5647A | Tn5 DNA Library Preparation Kit (for Illumina, for 1 ng DNA) | 6 T |
BL5647B | Tn5 DNA Library Preparation Kit (for Illumina, for 1 ng DNA) | 12 T |
BL5647C | Tn5 DNA Library Preparation Kit (for Illumina, for 1 ng DNA) | 24 T |
BL5647D | Tn5 DNA Library Preparation Kit (for Illumina, for 1 ng DNA) | 96 T |
BL5648A | Tn5 DNA Library Preparation Kit (for Illumina, for 50 ng DNA) | 6 T |
BL5648B | Tn5 DNA Library Preparation Kit (for Illumina, for 50 ng DNA) | 12 T |
BL5648C | Tn5 DNA Library Preparation Kit (for Illumina, for 50 ng DNA) | 24 T |
BL5648D | Tn5 DNA Library Preparation Kit (for Illumina, for 50 ng DNA) | 96 T |
DNA Library Preparation Kit
- Simple operation: optimized ligation system reduces pipetting steps - Efficient fragmentation enzyme: minimal bias, high library coverage - Broad sample compatibility: genomic DNA, full-length cDNA, FFPE DNA - Automated library preparation: supports high-throughput automated library construction |
Cat. No. | Description | Packaging |
BL5649A | DNA Library Preparation Kit (for Illumina Platform) | 6 T |
BL5649B | DNA Library Preparation Kit (for Illumina Platform) | 12 T |
BL5649C | DNA Library Preparation Kit (for Illumina Platform) | 24 T |
BL5649D | DNA Library Preparation Kit (for Illumina Platform) | 96 T |
Enzymatic Fragmentation DNA Library Preparation Kit
- Simple operation: fragmentation to adapter ligation completed in a single tube - Efficient fragmentation enzyme: minimal bias, high library coverage - Fewer steps: saves time and reduces bead usage - Broad sample compatibility: genomic DNA, full-length cDNA, FFPE DNA - Automated library preparation: supports high-throughput automated library construction |
Cat. No. | Description | Packaging |
BL5650A | Enzymatic Fragmentation DNA Library Preparation Kit (for Illumina Platform) | 6 T |
BL5650B | Enzymatic Fragmentation DNA Library Preparation Kit (for Illumina Platform) | 12 T |
BL5650C | Enzymatic Fragmentation DNA Library Preparation Kit (for Illumina Platform) | 24 T |
BL5650D | Enzymatic Fragmentation DNA Library Preparation Kit (for Illumina Platform) | 96 T |
DNA Selection Magnetic Beads
DNA Select Beads utilize imported magnetic beads with high binding capacity, fast magnetic response, and low sedimentation based on the Solid Phase Reversible Immobilization (SPRI) principle, combined with an optimized binding buffer. They are designed for nucleic acid purification and fragment size selection, offering high recovery efficiency and purity. The operation method, purification, and size selection performance are highly consistent with Beckman AMPure XP, making them suitable for both manual and automated workflows.
- Efficiently recovers nucleic acid fragments larger than 100 bp - Effectively removes dNTPs, primers, primer dimers, salts, and other impurities - Purifies both double-stranded and single-stranded DNA - Simpler, more efficient, and more economical than traditional column-based purification methods - Compatible with automated workstations for high-throughput sample preparation |
Cat. No. | Description | Packaging |
BL5651A | DNA Selection Magnetic Beads | 5mL |
BL5651B | DNA Selection Magnetic Beads | 60mL |
BL5651C | DNA Selection Magnetic Beads | 450mL |
