FGA-ZNFX1 Fusion FISH Probe
The FGA-ZNFX1 Fusion FISH Probe is used to confirm a fusion of the FGA and ZNFX1 genes. The fusion of the FGA and ZNFX1 genes has been associated with Liver Hepatocellular 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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| FGA-ZNFX1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-RERE | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-REOR | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-REGO | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-REGR | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-REAQ | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-ORRE | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-OROR | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-ORGO | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-ORAQ | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-GORE | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-GOOR | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-GOGO | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-GOGR | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-GOAQ | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-GRRE | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-GROR | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-GRGO | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-GRGR | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-GRAQ | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-AQRE | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-AQOR | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-AQGO | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-AQGR | 20 (40 μL) | 200 μL |
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| FGA-ZNFX1-20-AQAQ | 20 (40 μL) | 200 μL |
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FGA Gene Summary
This gene encodes the alpha subunit of the coagulation factor fibrinogen, which is a component of the blood clot. Following vascular injury, the encoded preproprotein is proteolytically processed by thrombin during the conversion of fibrinogen to fibrin. Mutations in this gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia, afibrinogenemia and renal amyloidosis. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that undergoes proteolytic processing. [provided by RefSeq, Jan 2016]
Gene Name: Fibrinogen Alpha Chain
Chromosome: CHR4: 155504279 -155511897
Locus: 4q31.3
ZNFX1 Gene Summary
The Zinc Finger NFX1-type Containing 1 (ZNFX1) gene is located on chr20 :47862438-47894756 at 20q13.13.
Gene Name: Zinc Finger NFX1-type Containing 1
Chromosome: CHR20: 47862438 -47894756
Locus: 20q13.13
Gene Diseases
The FGA ZNFX1 Fusion has been associated with the following diseases:
| Disease Name |
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| Liver Hepatocellular Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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