EVC2-CPM Fusion FISH Probe
The EVC2-CPM Fusion FISH Probe is used to confirm a fusion of the EVC2 and CPM genes. The fusion of the EVC2 and CPM genes has been associated with Sarcoma. 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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| EVC2-CPM-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-RERE | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-REOR | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-REGO | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-REGR | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-REAQ | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-ORRE | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-OROR | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-ORGO | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-ORAQ | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-GORE | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-GOOR | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-GOGO | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-GOGR | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-GOAQ | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-GRRE | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-GROR | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-GRGO | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-GRGR | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-GRAQ | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-AQRE | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-AQOR | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-AQGO | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-AQGR | 20 (40 μL) | 200 μL |
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| EVC2-CPM-20-AQAQ | 20 (40 μL) | 200 μL |
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CPM Gene Summary
The protein encoded by this gene is a membrane-bound arginine/lysine carboxypeptidase. Its expression is associated with monocyte to macrophage differentiation. This encoded protein contains hydrophobic regions at the amino and carboxy termini and has 6 potential asparagine-linked glycosylation sites. The active site residues of carboxypeptidases A and B are conserved in this protein. Three alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Carboxypeptidase M
Chromosome: CHR12: 69244955 -69357020
Locus: 12q15
EVC2 Gene Summary
This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
Gene Name: EvC Ciliary Complex Subunit 2
Chromosome: CHR4: 5564145 -5711275
Locus: 4p16.2
Gene Diseases
The EVC2 CPM Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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