GSN-CTNNB1 Fusion FISH Probe
The GSN-CTNNB1 Fusion FISH Probe is used to confirm a fusion of the GSN and CTNNB1 genes. The fusion of the GSN and CTNNB1 genes has been associated with Thyroid Carcinoma. 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| GSN-CTNNB1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-RERE | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-REOR | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-REGO | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-REGR | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-REAQ | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-ORRE | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-OROR | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-ORGO | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-ORAQ | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-GORE | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-GOOR | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-GOGO | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-GOGR | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-GOAQ | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-GRRE | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-GROR | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-GRGO | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-GRGR | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-GRAQ | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-AQRE | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-AQOR | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-AQGO | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-AQGR | 20 (40 μL) | 200 μL |
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| GSN-CTNNB1-20-AQAQ | 20 (40 μL) | 200 μL |
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CTNNB1 Gene Summary
The protein encoded by this gene is part of a complex of proteins that constitute adherens junctions (AJs). AJs are necessary for the creation and maintenance of epithelial cell layers by regulating cell growth and adhesion between cells. The encoded protein also anchors the actin cytoskeleton and may be responsible for transmitting the contact inhibition signal that causes cells to stop dividing once the epithelial sheet is complete. Finally, this protein binds to the product of the APC gene, which is mutated in adenomatous polyposis of the colon. Mutations in this gene are a cause of colorectal cancer (CRC), pilomatrixoma (PTR), medulloblastoma (MDB), and ovarian cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]
Gene Name: Catenin Beta 1
Chromosome: CHR3: 41240941 -41281939
Locus: 3p22.1
GSN Gene Summary
The protein encoded by this gene binds to the "plus" ends of actin monomers and filaments to prevent monomer exchange. The encoded calcium-regulated protein functions in both assembly and disassembly of actin filaments. Defects in this gene are a cause of familial amyloidosis Finnish type (FAF). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Gelsolin
Chromosome: CHR9: 124030379 -124095120
Locus: 9q33.2
Gene Diseases
The GSN CTNNB1 Fusion has been associated with the following diseases:
| Disease Name |
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| Thyroid Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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