CRISPR/Cas9 knockout, AAVS1 knock-in, CRISPRa gene activation, and CRISPRi gene repression. Validated lentiviral delivery with single clone screening and sequencing confirmation.

Lentivirus and retrovirus packaging at regular (10⁷), high (10⁸), and ultra-high (10⁹) IFU/ml titers. VSV-G pseudotyped. qPCR titration QC.

From DNA sequence to purified protein. Expression system optimization in E. coli, yeast, or mammalian hosts. Risk-free — payment upon successful delivery.

Custom iPSC generation from PBMCs or CD34+ hematopoietic cells. Non-integrating episomal reprogramming. Risk-free — payment upon successful delivery.

Custom stable cell lines and immortalized primary cells — reporter, overexpression, TET-inducible, and SV40/hTERT variants. Validated across human, mouse, rat, and large animal species. Risk-free — invoiced upon success.

Custom gene synthesis (50 bp–200 kb) with 100% sequence accuracy and free codon optimization. DNA oligos, RNA oligos, sgRNA, siRNA/miRNA, modified oligos, and diagnostic probes.