MVK-CPM Fusion FISH Probe
The MVK-CPM Fusion FISH Probe is used to confirm a fusion of the MVK and CPM genes. The fusion of the MVK 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. 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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| MVK-CPM-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-RERE | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-REOR | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-REGO | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-REGR | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-REAQ | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-ORRE | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-OROR | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-ORGO | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-ORAQ | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-GORE | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-GOOR | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-GOGO | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-GOGR | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-GOAQ | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-GRRE | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-GROR | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-GRGO | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-GRGR | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-GRAQ | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-AQRE | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-AQOR | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-AQGO | 20 (40 μL) | 200 μL |
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| MVK-CPM-20-AQGR | 20 (40 μL) | 200 μL |
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| MVK-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
MVK Gene Summary
This gene encodes the peroxisomal enzyme mevalonate kinase. Mevalonate is a key intermediate, and mevalonate kinase a key early enzyme, in isoprenoid and sterol synthesis. Mevalonate kinase deficiency caused by mutation of this gene results in mevalonic aciduria, a disease characterized psychomotor retardation, failure to thrive, hepatosplenomegaly, anemia and recurrent febrile crises. Defects in this gene also cause hyperimmunoglobulinaemia D and periodic fever syndrome, a disorder characterized by recurrent episodes of fever associated with lymphadenopathy, arthralgia, gastrointestinal dismay and skin rash. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]
Gene Name: Mevalonate Kinase
Chromosome: CHR12: 110011499 -110035071
Locus: 12q24.11
Gene Diseases
The MVK 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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