System Biosciences
PinPoint-FC Murine iPSC Platform Cell Line for Targeted Gene Insertion (with PinPoint site already placed)
- SKU:
- PIN340iPS-1
- Availability:
- Usually Shipped in 5 Working Days
- Size:
- >2x10^5 cells
- Shipping Temperature:
- Dry Ice
Description
PinPoint-FC Murine iPSC Platform Cell Line for Targeted Gene Insertion (with PinPoint site already placed). Cat# PIN340iPS. Supplier: SBI System Biosciences
Products
Overview
With the PinPoint-FC Murine iPSC Platform Cell Line for Targeted Gene Insertion you can skip the first step of the PinPoint Targeted Integration workflow because SBI’s already done it for you. This mouse fibroblast iPS cell line comes with a PinPoint attP site already placed and validated to be present in single copy, so you can simply co-transfect with the PinPoint Integrase Expression Vector and an appropriate PinPoint Donor Vector.
With the PinPoint-FC Murine iPSC Platform Cell Line for Targeted Gene Insertion, generating isogenic cell lines becomes a straightforward, one-step process that can be easily implanted as a high-throughput assay.
How It Works
Move a step ahead with the PinPoint-FC293T Platform Cell Line
Engineering cells with the PinPoint-FC 293T Platform Cell Line for Targeted Gene Insertion simplifies a two-step process into a single step. You can skip the placement of the PinPoint attP site and associated validation to verify copy number, and move straight to the insertion of your expression cassette with the PinPoint Donor Vector and PinPoint Integrase.
The PinPoint Integrase mediates a recombination event between the PinPoint attB site (located on the PinPoint Vector) and the PinPoint attP site. Because the PinPoint Integrase only recognizes the pre-placed PinPoint attP site, you get very stringent control of integration location.
Supporting Data
See the PinPoint Targeted Integration System in action
Figure 1. Efficient placement of the PinPoint attP site using the PhiC31 System. Step 1 of the PinPoint Targeted Integration System—the PinPoint attP site was placed into HEK293 cells using the PinPoint-FC Placement Vector (Cat.# PIN300A-1) and the PhiC31 Integrase (Cat.# FC200PA-1). Positive cells were selected with G418 (neomycin resistance) for fourteen days and six separate lines were picked and expanded. After eleven days, the cells were fixed and stained with a solution of 50% methanol plus 1% methylene blue. The plates were washed twice with PBS and allowed to air dry. Only the plate of cells that were transfected with the PhiC31 Integrase Expression Plasmid showed a robust number of cells.