Core services are offered to you by GoEditStem cores as detailed below. Please contact the relevant core for enquiries.
GoEditStem platform cores offer a variety of services related to creating CRISPR knock-outs in cells.
FinGEEC
Consultation
BSCC
GBU
Services related to CRISPR animal models are provided by Comprehensive Model Organisms platform
HelVi-BVC
HelVi-AAV
FinGEEC
BSCC
NiPS
Genome Biology Unit hosts clone libraries and provides cloning services to a variety of vectors. GBU also works with pooled DNA libraries.
Transverse workflows are services provided by more than one core unit of the GoEditStem platform. Our aim is to deliver the customer the custom designed end product and coordinate the steps within the platform. Please contact
Generation of transgene-expressing cells is done by
Step 1. Selecting a construct of interest from
Step 2. Recombinant virus preps is generated using the selected construct
Step 3. a) Customer provides mycoplasma-tested target cells to
Step 3. b) Kill-curve for antibiotic selection is generated
Step 4. Transduction of the target cells
Step 5. Selection and expansion of the transduced cells
Step 6: Customer receives two frozen ampoules per each construct of Biosafety-level one (BSL1) ready cells
NOTE
Only need the virus prep? Choose steps 1-2
Already have your virus? Choose steps 3-6
Generation of CRISPR-edited cells is done by
Step 1. Choose your construct with the guide from
Step 2. Recombinant virus preps is generated using the selected construct (
Step 3. Customer provides mycoplasma-tested target cells
Step 4. Delivery of the editing components into the target cells via transfection, electroporation, or transduction
Step 6. Selection expansion of edited cells
NOTE
You can also provide your own construct or virus and start from step 3.
Step 1, choose one:
A) Select a cDNA clone from the Gateway-compatible
B) Obtain a Gateway-compatible pENTR clone with your favourite cDNA from a commercial supplier.
C) Any cDNA template can be converted to Gateway system using PCR in
(ideal cDNA length 1-2,5 kb)
Step 2: The cDNA is cloned to pAAV-Gateway using Gateway cloning.
Step 3: Helvi-AAV produces the virus prep of your choice. You can select the AAV serotype based on the desired cell-type specificity, and the scale of rAAV particle production (small scale 0,3 ml, large-scale 3 ml).
NOTE
You can also obtain an AAV vector containing your cDNA of interest from a commercial source and deliver it directly to HelVI-AAV.
Instruments and facilities: GoEditStem hosts a variety of facilities and instruments to support your research, as detailed below.
The IncuCyte S3 continuously acquires and analyzes images, supporting up to six microplates simultaneously. Users can schedule experiments with varying image acquisition frequencies and magnifications. The system also allows remote access with unlimited free licenses. Available IncuCyte S3 modules include Standard, Scratch Wound, Whole Well, Dilution Cloning, and Chemotaxis, along with Basic Analyzer and Neurotrack modules for analysis.
For in vitro electrophysiology,
The 4D-Nucleofector® Core Unit and X Unit functional module support Nucleofection of various cell numbers (2 x 10^4 to 2 x 10^7) across different formats. Cell type-specific optimized protocols or recommendations can be found in Lonza's knowledge database, where the best Nucleofection conditions are outlined. Additionally, Lonza provides expertise and guidance for the handling of specific cell types, sharing valuable insights for improving transfection outcomes.
This device can be loaned from
FinGEEC core runs a digital slide scanning service (Pannoramic 250 FLASH III, 3DHISTECH) for both bright-field and fluorescent slides using either 20x or 40x air objectives. See our
New instrument alert!
FinGEEC will provide nucleofection optimization services, including equipment rental with reagents and full optimization, at the beginning of 2025.
Did you not find what you were looking for? Need more information? Contact us to discuss how we could help your research.
You can contact the cores directly or reach us all at