plexWell™ LP 384
$4,992.00
($13.00 Per Sample)plexWell™ LP 384 (low-pass whole genome) Benefits:
- plexWell NGS multiplexed library generation kit for Illumina®
- Assay-ready 96-well fully-skirted low-profile PCR plates (4 x 96)
- 768 (96 x 8) unique barcode combinations
- 2 sets of 4 pool barcodes – PB Set A or B
- Volume-based pricing
* If you need to multiplex more than 768 samples, please contact us at [email protected]
Description:
- Same enhanced plexWell workflow engineered for low-pass whole genome library prep and sequencing
- Kit contains major reagents necessary to prepare libraries including Magwise™ paramagnetic beads (DNA polymerase not included)
- Efficient library prep for more than one 96-well plate of samples
- Normalizes input DNA over wide input range of 5-25 ng
- Volume-based pricing (save 30-50% on total lab costs)
Recommended Application:
- Low-depth whole genome/GBS coupled with an imputation and analysis software
plexWell™ Library Prep Workflow:
plexWell™ Library Prep Chemistry:
Specifications:
-
- Time-to-prepare a multiplexed library from 96 samples:
- Hands-on time: 50 min
- Total elapsed time: 3 hrs
- Recommended input: 5-25 ng of genomic DNA per sample (n=96)
- Expected Results:
- Library Yield: 750 – 1500 fmoles of purified multiplexed library
- Estimated Duplication Rate: 10% per 10M paired-reads on human gDNA
- Substantial normalization: Typically <2.5-fold range (min to max) in read count across all 96 samples
- Compatibility with Illumina® sequencing systems:
- Compatible with Illumina MiSeq®, NextSeq®, HiSeq® and NovaSeq® instrument platforms
- Time-to-prepare a multiplexed library from 96 samples: