MPDU1-C22ORF13 Fusion FISH Probe
The MPDU1-C22ORF13 Fusion FISH Probe is used to confirm a fusion of the MPDU1 and C22ORF13 genes. The fusion of the MPDU1 and C22ORF13 genes has been associated with Bladder Urothelial Carcinoma. 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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| MPDU1-C22ORF13-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-RERE | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-REOR | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-REGO | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-REGR | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-REAQ | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-ORRE | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-OROR | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-ORGO | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-ORAQ | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-GORE | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-GOOR | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-GOGO | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-GOGR | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-GOAQ | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-GRRE | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-GROR | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-GRGO | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-GRGR | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-GRAQ | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-AQRE | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-AQOR | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-AQGO | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-AQGR | 20 (40 μL) | 200 μL |
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| MPDU1-C22ORF13-20-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
Gene Diseases
The MPDU1 C22ORF13 Fusion has been associated with the following diseases:
| Disease Name |
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| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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