C22ORF13-MB Fusion FISH Probe
The C22ORF13-MB Fusion FISH Probe is used to confirm a fusion of the C22ORF13 and MB genes. The fusion of the C22ORF13 and MB genes has been associated with Uveal Melanoma. 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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| C22ORF13-MB-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-RERE | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-REOR | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-REGO | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-REGR | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-REAQ | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-ORRE | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-OROR | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-ORGO | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-ORAQ | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-GORE | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-GOOR | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-GOGO | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-GOGR | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-GOAQ | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-GRRE | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-GROR | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-GRGO | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-GRGR | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-GRAQ | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-AQRE | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-AQOR | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-AQGO | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-AQGR | 20 (40 μL) | 200 μL |
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| C22ORF13-MB-20-AQAQ | 20 (40 μL) | 200 μL |
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MB Gene Summary
This gene encodes a member of the globin superfamily and is expressed in skeletal and cardiac muscles. The encoded protein is a haemoprotein contributing to intracellular oxygen storage and transcellular facilitated diffusion of oxygen. At least three alternatively spliced transcript variants encoding the same protein have been reported. [provided by RefSeq, Jul 2008]
Gene Name: Myoglobin
Chromosome: CHR22: 36002810 -36019401
Locus: 22q12.3
Gene Diseases
The C22ORF13 MB Fusion has been associated with the following diseases:
| Disease Name |
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| Uveal Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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