C2CD3-ABCA13 Fusion FISH Probe
The C2CD3-ABCA13 Fusion FISH Probe is used to confirm a fusion of the C2CD3 and ABCA13 genes. The fusion of the C2CD3 and ABCA13 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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| C2CD3-ABCA13-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-RERE | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-REOR | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-REGO | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-REGR | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-REAQ | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-ORRE | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-OROR | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-ORGO | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-ORAQ | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-GORE | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-GOOR | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-GOGO | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-GOGR | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-GOAQ | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-GRRE | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-GROR | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-GRGO | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-GRGR | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-GRAQ | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-AQRE | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-AQOR | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-AQGO | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-AQGR | 20 (40 μL) | 200 μL |
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| C2CD3-ABCA13-20-AQAQ | 20 (40 μL) | 200 μL |
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C2CD3 Gene Summary
This gene encodes a protein that functions as a regulator of centriole elongation. Studies of the orthologous mouse protein show that it promotes centriolar distal appendage assembly and is also required for the recruitment of other ciliogenic proteins, including intraflagellar transport proteins. Mutations in this gene cause orofaciodigital syndrome XIV (OFD14), a ciliopathy resulting in malformations of the oral cavity, face and digits. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2014]
Gene Name: C2 Calcium Dependent Domain Containing 3
Chromosome: CHR11: 73745479 -73882064
Locus: 11q13.4
ABCA13 Gene Summary
In human, the ATP-binding cassette (ABC) family of transmembrane transporters has at least 48 genes and 7 gene subfamilies. This gene is a member of ABC gene subfamily A (ABCA). Genes within the ABCA family typically encode several thousand amino acids. Like other ABC transmembrane transporter proteins, this protein has 12 or more transmembrane alpha-helix domains that likely arrange to form a single central chamber with multiple substrate binding sites. It is also predicted to have two large extracellular domains and two nucleotide binding domains as is typical for ABCA proteins. Alternative splice variants have been described but their biological validity has not been demonstrated.[provided by RefSeq, Mar 2009]
Gene Name: ATP Binding Cassette Subfamily A Member 13
Chromosome: CHR7: 48211056 -48687091
Locus: 7p12.3
Gene Diseases
The C2CD3 ABCA13 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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