• 17
• 0

What is the unit of the spatial coordinates from the Seeker Primary Analysis Pipeline? How do I convert them to µm?

• 250
• 0

Are there any special considerations that must be taken into account when performing AMPure XP purification on libraries prepared with the ThruPLEX DNA-Seq Kit?

• 254
• 0

How does the smaller number of UMI (144) provide a complete diversity of tagged molecules in ThruPLEX Tag-seq kits?

• 283
• 0

Are the PicoPLEX Gold libraries compatible with the Illumina Patterned Flow cell sequencing platforms such as Novaseq 6000?

• 197
• 0

What makes the PicoPLEX Single Cell WGA Kit suited for SNP genotyping?

• 199
• 0

Sigma-Aldrich sells a GenomePlex WGA kit. Does it contain the same technology as the PicoPLEX Single Cell WGA Kit?

• 199
• 0

What are the indexing options for the PicoPLEX Gold Single Cell DNA-Seq Kit?

• 205
• 0

Can we use barcodes designed in our laboratory for PicoPLEX Gold Single Cell DNA-Seq Kit?

• 199
• 0

Do we have to purchase barcoded oligonucleotides separately for PicoPLEX Gold Single Cell DNA-Seq Kit?

• 255
• 0

Can I use the PicoPLEX Gold Single Cell DNA-Seq Kit for whole-genome de novo sequencing from a single cell?

• 237
• 0

Can I use indexing primers from vendors other than Takara Bio USA?

• 245
• 0

What is the purpose of the DNA SMART Custom Read2 Seq Primer, include in the DNA SMART™ ChIP-Seq Kit?

• 223
• 0

Can the DNA SMART Poly(dA) Primer  anneal to internal /A -rich sequences in the genomic DNA?

• 222
• 0

Why is there no size selection and clean-up not before the PCR step within the DMA SMART ChIP-Seq protocol as in other kits?

• 226
• 0

How does the ChIP Elute work?

• 246
• 0

Can the Guide-it SNP Screening assay be used to distinguish homozygotes from heterozygotes?

• 273
• 0

How does Guide-it Flapase detect the edited nucleotide?

• 250
• 0

How can I increase the frequencies of edited clones with only one modified allele and the other one encoding the wild-type sequence?