C10ORF26-ADAMTS2 Fusion FISH Probe
The C10ORF26-ADAMTS2 Fusion FISH Probe is used to confirm a fusion of the C10ORF26 and ADAMTS2 genes. The fusion of the C10ORF26 and ADAMTS2 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| C10ORF26-ADAMTS2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-RERE | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-REOR | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-REGO | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-REGR | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-REAQ | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-ORRE | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-OROR | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-ORGO | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-ORAQ | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-GORE | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-GOOR | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-GOGO | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-GOGR | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-GOAQ | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-GRRE | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-GROR | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-GRGO | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-GRGR | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-GRAQ | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-AQRE | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-AQOR | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-AQGO | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-AQGR | 20 (40 μL) | 200 μL |
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| C10ORF26-ADAMTS2-20-AQAQ | 20 (40 μL) | 200 μL |
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ADAMTS2 Gene Summary
This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]
Gene Name: ADAM Metallopeptidase With Thrombospondin Type 1 Motif 2
Chromosome: CHR5: 178537851 -178772431
Locus: 5q35.3
Gene Diseases
The C10ORF26 ADAMTS2 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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