EPB41-YTHDF2 Fusion FISH Probe
The EPB41-YTHDF2 Fusion FISH Probe is used to confirm a fusion of the EPB41 and YTHDF2 genes. The fusion of the EPB41 and YTHDF2 genes has been associated with Uterine Carcinosarcoma, and Pheochromocytoma And Paraganglioma. 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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| EPB41-YTHDF2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-RERE | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-REOR | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-REGO | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-REGR | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-REAQ | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-ORRE | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-OROR | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-ORGO | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-ORAQ | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-GORE | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-GOOR | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-GOGO | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-GOGR | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-GOAQ | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-GRRE | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-GROR | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-GRGO | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-GRGR | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-GRAQ | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-AQRE | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-AQOR | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-AQGO | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-AQGR | 20 (40 μL) | 200 μL |
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| EPB41-YTHDF2-20-AQAQ | 20 (40 μL) | 200 μL |
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EPB41 Gene Summary
The protein encoded by this gene, together with spectrin and actin, constitute the red cell membrane cytoskeletal network. This complex plays a critical role in erythrocyte shape and deformability. Mutations in this gene are associated with type 1 elliptocytosis (EL1). Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Oct 2009]
Gene Name: Erythrocyte Membrane Protein Band 4.1
Chromosome: CHR1: 29213602 -29446558
Locus: 1p35.3
YTHDF2 Gene Summary
This gene encodes a member of the YTH (YT521-B homology) superfamily containing YTH domain. The YTH domain is typical for the eukaryotes and is particularly abundant in plants. The YTH domain is usually located in the middle of the protein sequence and may function in binding to RNA. In addition to a YTH domain, this protein has a proline rich region which may be involved in signal transduction. An Alu-rich domain has been identified in one of the introns of this gene, which is thought to be associated with human longevity. In addition, reciprocal translocations between this gene and the Runx1 (AML1) gene on chromosome 21 has been observed in patients with acute myeloid leukemia. This gene was initially mapped to chromosome 14, which was later turned out to be a pseudogene. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Oct 2012]
Gene Name: YTH N6-methyladenosine RNA Binding Protein 2
Chromosome: CHR1: 29063132 -29096287
Locus: 1p35.3
Gene Diseases
The EPB41 YTHDF2 Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Carcinosarcoma |
| Pheochromocytoma And Paraganglioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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