• 228
• 0

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

• 128
• 0

Is PicoPLEX WGA/DNA-seq kit compatible with plant samples such as Pollen?

• 189
• 0

Is the PicoPLEX WGA kit efficient for bacteria?

• 176
• 0

Can I perform additional amplification of libraries prepared with the ThruPLEX DNA-Seq Kit if the concentrations or yields of the libraries are insufficient?

• 206
• 0

Can I use the PicoPLEX WGA kit downstream of the RT (reverse transcription) reaction to analyze clinical samples infected by various pathogens – DNA and RNA based viruses and bacteria?

• 207
• 0

Where can I find information about a kit for preparing randomly fragmented genomic DNA for use with the ThruPLEX DNA-Seq Kit?

• 290
• 0

Can I make the product of the PicoPLEX Single Cell WGA Kit NGS-ready?

• 236
• 0

Can the Guide-it SNP Screening Kit only be used to detect single-nucleotide substitutions? Would it be suitable for detecting longer insertions?

• 227
• 0

How clean does the PCR of the genomic target sequence need to be for the Guide-it SNP Screening Kit?

• 224
• 0

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

• 230
• 0

What are additional methods for improving HDR efficiency?

• 209
• 0

Does the HDR insertion site need to be directly next to the PAM?

• 305
• 0

Is it helpful to use HDR templates that introduce silent mutations in the PAM sequence or sgRNA seeding region?

• 406
• 0

What are optimal lengths for HDR template homology arms?

• 234
• 0

With ssODN or ssDNA, is it advantageous to use HDR templates that are homologous to the sense or antisense strand at the genomic target region?

• 240
• 0

Where can I find all the vector maps for the Guide-it CRISPR Genome-Wide sgRNA Library System?

• 241
• 0

Does every sgRNA in the library work?

• 281
• 0

What is the Brunello algorithm that was used to create the library?