CNOT1-RASSF8 Fusion FISH Probe
The CNOT1-RASSF8 Fusion FISH Probe is used to confirm a fusion of the CNOT1 and RASSF8 genes. The fusion of the CNOT1 and RASSF8 genes has been associated with Breast Invasive 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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| CNOT1-RASSF8-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-RERE | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-REOR | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-REGO | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-REGR | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-REAQ | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-ORRE | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-OROR | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-ORGO | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-ORAQ | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-GORE | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-GOOR | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-GOGO | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-GOGR | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-GOAQ | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-GRRE | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-GROR | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-GRGO | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-GRGR | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-GRAQ | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-AQRE | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-AQOR | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-AQGO | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-AQGR | 20 (40 μL) | 200 μL |
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| CNOT1-RASSF8-20-AQAQ | 20 (40 μL) | 200 μL |
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RASSF8 Gene Summary
This gene encodes a member of the Ras-assocation domain family (RASSF) of tumor suppressor proteins. This gene is essential for maintaining adherens junction function in epithelial cells and has a role in epithelial cell migration. It is a lung tumor suppressor gene candidate. A chromosomal translocation t(12;22)(p11.2;q13.3) leading to the fusion of this gene and the FBLN1 gene is found in a complex type of synpolydactyly. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]
Gene Name: Ras Association Domain Family Member 8
Chromosome: CHR12: 26111963 -26232825
Locus: 12p12.1
CNOT1 Gene Summary
The CCR4-NOT Transcription Complex Subunit 1 (CNOT1) gene is located on chr16 :58553854-58663750 at 16q21.
Gene Name: CCR4-NOT Transcription Complex Subunit 1
Chromosome: CHR16: 58553854 -58663750
Locus: 16q21
Gene Diseases
The CNOT1 RASSF8 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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