TEAD1-INSC Fusion FISH Probe
The TEAD1-INSC Fusion FISH Probe is used to confirm a fusion of the TEAD1 and INSC genes. The fusion of the TEAD1 and INSC genes has been associated with Sarcoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** This product is for in vitro and research use only. This product is not intended for diagnostic use. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
SKU | Test Kits | Buffer | Dye Color | Order Now |
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TEAD1-INSC-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-RERE | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-REOR | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-REGO | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-REGR | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-REAQ | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-ORRE | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-OROR | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-ORGO | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-ORAQ | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-GORE | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-GOOR | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-GOGO | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-GOGR | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-GOAQ | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-GRRE | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-GROR | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-GRGO | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-GRGR | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-GRAQ | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-AQRE | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-AQOR | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-AQGO | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-AQGR | 20 (40 μL) | 200 μL | ||
TEAD1-INSC-20-AQAQ | 20 (40 μL) | 200 μL |
TEAD1 Gene Summary
This gene encodes a ubiquitous transcriptional enhancer factor that is a member of the TEA/ATTS domain family. This protein directs the transactivation of a wide variety of genes and, in placental cells, also acts as a transcriptional repressor. Mutations in this gene cause Sveinsson's chorioretinal atrophy. Additional transcript variants have been described but their full-length natures have not been experimentally verified. [provided by RefSeq, May 2010]
Gene Name: TEA Domain Transcription Factor 1
Chromosome: CHR11: 12695968 -12966284
Locus: 11p15.3
INSC Gene Summary
In Drosophila, neuroblasts divide asymmetrically into another neuroblast at the apical side and a smaller ganglion mother cell on the basal side. Cell polarization is precisely regulated by 2 apically localized multiprotein signaling complexes that are tethered by Inscuteable, which regulates their apical localization (Izaki et al., 2006 [PubMed 16458856]).[supplied by OMIM, Mar 2008]
Gene Name: INSC, Spindle Orientation Adaptor Protein
Chromosome: CHR11: 15133969 -15268754
Locus: 11p15.2
Gene Diseases
The TEAD1 INSC Fusion has been associated with the following diseases:
Disease Name |
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Sarcoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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