EFTUD2-PLEKHM1 Fusion FISH Probe
The EFTUD2-PLEKHM1 Fusion FISH Probe is used to confirm a fusion of the EFTUD2 and PLEKHM1 genes. The fusion of the EFTUD2 and PLEKHM1 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. 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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| EFTUD2-PLEKHM1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-RERE | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-REOR | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-REGO | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-REGR | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-REAQ | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-ORRE | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-OROR | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-ORGO | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-ORAQ | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-GORE | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-GOOR | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-GOGO | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-GOGR | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-GOAQ | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-GRRE | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-GROR | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-GRGO | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-GRGR | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-GRAQ | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-AQRE | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-AQOR | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-AQGO | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-AQGR | 20 (40 μL) | 200 μL |
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| EFTUD2-PLEKHM1-20-AQAQ | 20 (40 μL) | 200 μL |
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EFTUD2 Gene Summary
This gene encodes a GTPase which is a component of the spliceosome complex which processes precursor mRNAs to produce mature mRNAs. Mutations in this gene are associated with mandibulofacial dysostosis with microcephaly. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]
Gene Name: Elongation Factor Tu GTP Binding Domain Containing 2
Chromosome: CHR17: 42927654 -42976993
Locus: 17q21.31
PLEKHM1 Gene Summary
The protein encoded by this gene is essential for bone resorption, and may play a critical role in vesicular transport in the osteoclast. Mutations in this gene are associated with autosomal recessive osteopetrosis type 6 (OPTB6). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2009]
Gene Name: Pleckstrin Homology And RUN Domain Containing M1
Chromosome: CHR17_ctg5_hap1: 128327 -183214
Locus: 17q21.31
Gene Diseases
The EFTUD2 PLEKHM1 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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