Library Construction Kits
GeneRulor library construction kits provide a complete range of NGS library construction solutions spanning universal, rapid and application-specific workflows. Its core lies in two major technological platforms: BLT and Fast Tagment. The GeneRulor BLT DNA Library Construction Kit adopts the classic and robust Bridge, Ligate and Tag (BLT) workflow, featuring broad sample compatibility. It is particularly suitable for complex or degraded samples such as FFPE, and can generate libraries with high yield and excellent uniformity, making it the universal first choice for prioritizing data quality. For high-efficiency library construction needs, the Fast Tagment DNA Rapid Library Construction Kit leverages transposase to enable a "single-tube" workflow, drastically shortening the entire library construction time to 1–2 hours. It is also available in dedicated versions optimized for the two mainstream sequencing platforms—Illumina and MGI (BGI Genomics)—offering an extremely convenient option for high-throughput and routine sample sequencing. In addition, the product line includes application-specific solutions for cutting-edge research, such as the GeneRulor ATAC-seq Library Construction Kit, which provides a ready-to-use optimized workflow for chromatin accessibility studies. In summary, users can flexibly select the most suitable product based on sample quality, sequencing platform, project timeline (choose BLT for quality priority, Fast Tagment for efficiency priority), and specific research objectives (e.g., select the ATAC-seq dedicated kit for epigenetics research).
Library Construction Kit Types
GeneRulor BLT DNA Library
Preparation Kit
Fast Tagment DNA Library
PrepKit For Illumina
GeneRulor ATAC-seq Library
PrepKit For Illumina
Fast Tagment DNA Library
PrepKit For MGI
Service Advantages
Rapid: The entire library construction takes only 2 hours.
Stable: Reliable library construction results are achievable for all types of double-stranded DNA samples.
Easy to operate: Single-tube operation with simultaneous DNA fragmentation and adapter ligation.
High efficiency: A dedicated polymerase paired with a carefully optimized reaction system boosts the efficiency of library amplification.
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