GBE1-ZNF569 Fusion FISH Probe
The GBE1-ZNF569 Fusion FISH Probe is used to confirm a fusion of the GBE1 and ZNF569 genes. The fusion of the GBE1 and ZNF569 genes has been associated with Uterine Carcinosarcoma. 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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| GBE1-ZNF569-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-RERE | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-REOR | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-REGO | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-REGR | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-REAQ | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-ORRE | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-OROR | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-ORGO | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-ORAQ | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-GORE | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-GOOR | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-GOGO | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-GOGR | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-GOAQ | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-GRRE | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-GROR | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-GRGO | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-GRGR | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-GRAQ | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-AQRE | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-AQOR | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-AQGO | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-AQGR | 20 (40 μL) | 200 μL |
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| GBE1-ZNF569-20-AQAQ | 20 (40 μL) | 200 μL |
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GBE1 Gene Summary
The protein encoded by this gene is a glycogen branching enzyme that catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on the same or a neighboring glycogen chain. Branching of the chains is essential to increase the solubility of the glycogen molecule and, consequently, in reducing the osmotic pressure within cells. Highest level of this enzyme are found in liver and muscle. Mutations in this gene are associated with glycogen storage disease IV (also known as Andersen's disease). [provided by RefSeq, Jul 2008]
Gene Name: 1,4-alpha-glucan Branching Enzyme 1
Chromosome: CHR3: 81538849 -81810950
Locus: 3p12.2
ZNF569 Gene Summary
The Zinc Finger Protein 569 (ZNF569) gene is located on chr19 :37902059-37958339 at 19q13.12.
Gene Name: Zinc Finger Protein 569
Chromosome: CHR19: 37902059 -37958339
Locus: 19q13.12
Gene Diseases
The GBE1 ZNF569 Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Carcinosarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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