Nanodigmbio molecular biology reagents

NadPrep RNA & DNA Library Co-Preparation Module is developed for high-throughput sequencing platforms, enabling a single process for RNA & DNA co-preparation from mixed pathogenic microbial samples. This module consist of 1st Strand Synthesis, ...

NadPrep DNA Library Preparation Module v2 is designed for the preparation of high-quality libraries from double-stranded DNA (dsDNA) on Illumina® & MGI platforms. This A-T ligation-based kit offers a stable and efficient library preparation ...

On the basis of the latest version of Refseq (109, 2021) and the CCDS database, NEXome Core Panel has carefully selected some regions that are worthy of attention outside the database. At the same time, based on product continuity considerations, ...

NadPrep EZ DNA Library Preparation Kit v2 is designed for preparation of high-quality sequencing libraries from double-stranded DNA (dsDNA) on MGI and Illumina platforms. To simplify the experimental process, multiple processes were applied ...

NanOnco Plus Panel v3.0 targets the full coding regions from 620 genes (HLA genes included) of interest in solid tumor studies, a series of intron regions related to common fusions, classical microsatellite sequences, and chemotherapy-associated ...

HRR Panel v1.0 targets whole coding sequences of 35 DNA Homologous recombination repair (HRR) related genes. It can be used alone for HRR gene mutation analysis, as well as spike-in to HiSNP-series panel forHomologous Recombination Deficiency ...

NanoHema Panel v2.0 targets 481 genes associated with hematologic malignancies, comprehensively covering a wide range of genetic alterations including base substitutions, insertions/deletions, amplifications, and gene fusions. This panel ...

HLAtyping Panel v2.0 refers to the latest database (Version 3.50), and targets 11 HLA genes (Class I: HLA-A, B, C; Class II: HLADPA1,DPB1, DQA1, DAQB1, DRB1/3/4/5). The probe covers the full-length genome sequence of all alleles and supports ...

NEXome Mini Panel focuses on the exome associated with clinical inherited diseases, with probe coverage spanning a 16.1 Mb genomic region involving 5650 clinically significant genes and encompassing over 4000 genetic disorders. In comparison ...

NEXome XP Panel v1.0 is an enhanced extended whole exome capture Panel. On the basis of NEXome Core Panel, it provides expanded coverage of clinically relevant variants in non-coding genomic regions, and includes the GENCODE annotation ...