MPDU1-SPEM1 Fusion FISH Probe
The MPDU1-SPEM1 Fusion FISH Probe is used to confirm a fusion of the MPDU1 and SPEM1 genes. The fusion of the MPDU1 and SPEM1 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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| MPDU1-SPEM1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-RERE | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-REOR | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-REGO | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-REGR | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-REAQ | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-ORRE | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-OROR | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-ORGO | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-ORAQ | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-GORE | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-GOOR | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-GOGO | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-GOGR | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-GOAQ | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-GRRE | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-GROR | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-GRGO | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-GRGR | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-GRAQ | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-AQRE | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-AQOR | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-AQGO | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-AQGR | 20 (40 μL) | 200 μL |
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| MPDU1-SPEM1-20-AQAQ | 20 (40 μL) | 200 μL |
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MPDU1 Gene Summary
This gene encodes an endoplasmic reticulum membrane protein that is required for utilization of the mannose donor mannose-P-dolichol in the synthesis of lipid-linked oligosaccharides and glycosylphosphatidylinositols. Mutations in this gene result in congenital disorder of glycosylation type If. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]
Gene Name: Mannose-P-dolichol Utilization Defect 1
Chromosome: CHR17: 7486964 -7491527
Locus: 17p13.1
SPEM1 Gene Summary
The Spermatid Maturation 1 (SPEM1) gene is located on chr17 :7323678-7324951 at 17p13.1.
Gene Name: Spermatid Maturation 1
Chromosome: CHR17: 7323678 -7324951
Locus: 17p13.1
Gene Diseases
The MPDU1 SPEM1 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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