ESCO2-EPHX2 Fusion FISH Probe
The ESCO2-EPHX2 Fusion FISH Probe is used to confirm a fusion of the ESCO2 and EPHX2 genes. The fusion of the ESCO2 and EPHX2 genes has been associated with Ovarian Serous Cystadenocarcinoma. 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
SKU | Test Kits | Buffer | Dye Color | Order Now |
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ESCO2-EPHX2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-RERE | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-REOR | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-REGO | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-REGR | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-REAQ | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-ORRE | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-OROR | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-ORGO | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-ORAQ | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-GORE | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-GOOR | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-GOGO | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-GOGR | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-GOAQ | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-GRRE | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-GROR | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-GRGO | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-GRGR | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-GRAQ | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-AQRE | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-AQOR | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-AQGO | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-AQGR | 20 (40 μL) | 200 μL | ||
ESCO2-EPHX2-20-AQAQ | 20 (40 μL) | 200 μL |
EPHX2 Gene Summary
This gene encodes a member of the epoxide hydrolase family. The protein, found in both the cytosol and peroxisomes, binds to specific epoxides and converts them to the corresponding dihydrodiols. Mutations in this gene have been associated with familial hypercholesterolemia. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2012]
Gene Name: Epoxide Hydrolase 2
Chromosome: CHR8: 27348644 -27402486
Locus: 8p21.2-p21.1
ESCO2 Gene Summary
This gene encodes a protein that may have acetyltransferase activity and may be required for the establishment of sister chromatid cohesion during the S phase of mitosis. Mutations in this gene have been associated with Roberts syndrome. [provided by RefSeq, Jul 2008]
Gene Name: Establishment Of Sister Chromatid Cohesion N-acetyltransferase 2
Chromosome: CHR8: 27632057 -27662424
Locus: 8p21.1
Gene Diseases
The ESCO2 EPHX2 Fusion has been associated with the following diseases:
Disease Name |
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Ovarian Serous Cystadenocarcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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