The FAK reporter collection
SwitchGear Genomics offers genome-wide panels of transfection-ready, cell-based reporter assays including specific panels of focal adhesion kinase or FAK-relevant promoter reporters and FAK-relevant UTR reporters allowing you to accurately quantify transcriptional regulation, transcript stability, and translational efficiency of genes in the FAK signaling pathway. Uncover miRNA function and the effects of transcription binding in the full FAK pathway of genes.
FAK Pathway Products
FAK Canonical Pathway diagram | Click on the image for a larger view.
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SwitchGear offers promoter and UTR reporters for studying transcript regulation and stability. Custom pricing is available for orders of 10 or more constructs. Contact us!
View our genome-wide collection of promoter and UTR products in our online catalog, SwitchDB. |
Applications
The SwitchGear collection of FAK-relevant promoter reporters allows you to:
- Understand the mechanisms by which the pathway of genes is induced or repressed
- Quantify the functional consequences of transcription factor binding – while many other technologies give a qualitative view of transcription factor presence, our promoter reporter assays quantify the effects of transcription factor binding.
- Confirm data from ChIP-chip or ChIP-sequencing experiments
- Measure the effect of sequence variants and mutagenesis on promoter function
- Screen for promoter activation in the full pathway under a multitude of conditions
See Promoter Reporter Collection for general information.
The SwitchGear collection of FAK-relevant 3′UTR reporters allows you to:
- Quantify the functional role of UTRs and miRNAs in post-transcriptional gene regulation under a multitude of conditions
- Validate expression data and computational predictions with miRNA functional studies
- Measure the effect of sequence variants and mutagenesis on 3′UTR function
- Screen for UTR and miRNA function in the full pathway
See UTR Reporter Collection for general information. Or search SwitchDB for specific miRNA candidates.



