C15ORF41-FAM98B Fusion FISH Probe
The C15ORF41-FAM98B Fusion FISH Probe is used to confirm a fusion of the C15ORF41 and FAM98B genes. The fusion of the C15ORF41 and FAM98B genes has been associated with Breast Invasive 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. 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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| C15ORF41-FAM98B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-RERE | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-REOR | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-REGO | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-REGR | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-REAQ | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-ORRE | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-OROR | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-ORGO | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-ORAQ | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-GORE | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-GOOR | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-GOGO | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-GOGR | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-GOAQ | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-GRRE | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-GROR | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-GRGO | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-GRGR | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-GRAQ | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-AQRE | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-AQOR | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-AQGO | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-AQGR | 20 (40 μL) | 200 μL |
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| C15ORF41-FAM98B-20-AQAQ | 20 (40 μL) | 200 μL |
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C15orf41 Gene Summary
This gene encodes a protein with two predicted helix-turn-helix domains. Mutations in this gene were found in families with congenital dyserythropoietic anemia type Ib. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]
Gene Name: Chromosome 15 Open Reading Frame 41
Chromosome: CHR15: 36871811 -37102449
Locus: 15q14
FAM98B Gene Summary
The Family With Sequence Similarity 98 Member B (FAM98B) gene is located on chr15 :38746327-38777063 at 15q14.
Gene Name: Family With Sequence Similarity 98 Member B
Chromosome: CHR15: 38746327 -38777063
Locus: 15q14
Gene Diseases
The C15ORF41 FAM98B Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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