SLC25A3-DDX27 Fusion FISH Probe
The SLC25A3-DDX27 Fusion FISH Probe is used to confirm a fusion of the SLC25A3 and DDX27 genes. The fusion of the SLC25A3 and DDX27 genes has been associated with Skin Cutaneous 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| SLC25A3-DDX27-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-RERE | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-REOR | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-REGO | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-REGR | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-REAQ | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-ORRE | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-OROR | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-ORGO | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-ORAQ | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-GORE | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-GOOR | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-GOGO | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-GOAQ | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-GROR | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-GRGR | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-GRAQ | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-AQRE | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-AQGO | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-AQGR | 20 (40 μL) | 200 μL |
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| SLC25A3-DDX27-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC25A3 Gene Summary
The protein encoded by this gene catalyzes the transport of phosphate into the mitochondrial matrix, either by proton cotransport or in exchange for hydroxyl ions. The protein contains three related segments arranged in tandem which are related to those found in other characterized members of the mitochondrial carrier family. Both the N-terminal and C-terminal regions of this protein protrude toward the cytosol. Multiple alternatively spliced transcript variants have been isolated. [provided by RefSeq, Jul 2008]
Gene Name: Solute Carrier Family 25 Member 3
Chromosome: CHR12: 98987402 -98995778
Locus: 12q23.1
DDX27 Gene Summary
DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein involved in the processing of 5.8S and 28S ribosomal RNAs. More specifically, the encoded protein localizes to the nucleolus, where it interacts with the PeBoW complex to ensure proper 3' end formation of 47S rRNA. [provided by RefSeq, Jan 2017]
Gene Name: DEAD-box Helicase 27
Chromosome: CHR20: 47835831 -47860614
Locus: 20q13.13
Gene Diseases
The SLC25A3 DDX27 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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