FOXO3-CHD7 Fusion FISH Probe
The FOXO3-CHD7 Fusion FISH Probe is used to confirm a fusion of the FOXO3 and CHD7 genes. The fusion of the FOXO3 and CHD7 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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| FOXO3-CHD7-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-RERE | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-REOR | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-REGO | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-REGR | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-REAQ | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-ORRE | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-OROR | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-ORGO | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-ORAQ | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-GORE | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-GOOR | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-GOGO | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-GOGR | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-GOAQ | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-GRRE | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-GROR | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-GRGO | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-GRGR | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-GRAQ | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-AQRE | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-AQOR | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-AQGO | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-AQGR | 20 (40 μL) | 200 μL |
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| FOXO3-CHD7-20-AQAQ | 20 (40 μL) | 200 μL |
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FOXO3 Gene Summary
This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. This gene likely functions as a trigger for apoptosis through expression of genes necessary for cell death. Translocation of this gene with the MLL gene is associated with secondary acute leukemia. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]
Gene Name: Forkhead Box O3
Chromosome: CHR6: 108881025 -109005971
Locus: 6q21
CHD7 Gene Summary
This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]
Gene Name: Chromodomain Helicase DNA Binding Protein 7
Chromosome: CHR8: 61591323 -61780586
Locus: 8q12.2
Gene Diseases
The FOXO3 CHD7 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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