EDC3-SNX29 Fusion FISH Probe
The EDC3-SNX29 Fusion FISH Probe is used to confirm a fusion of the EDC3 and SNX29 genes. The fusion of the EDC3 and SNX29 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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| EDC3-SNX29-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-RERE | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-REOR | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-REGO | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-REGR | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-REAQ | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-ORRE | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-OROR | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-ORGO | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-ORAQ | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-GORE | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-GOOR | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-GOGO | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-GOGR | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-GOAQ | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-GRRE | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-GROR | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-GRGO | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-GRGR | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-GRAQ | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-AQRE | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-AQOR | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-AQGO | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-AQGR | 20 (40 μL) | 200 μL |
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| EDC3-SNX29-20-AQAQ | 20 (40 μL) | 200 μL |
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EDC3 Gene Summary
This gene encodes a protein that is important in mRNA degradation. The encoded protein is a component of a decapping complex that promotes efficient removal of the monomethylguanosine (m7G) cap from mRNAs, as part of the 5' to 3' mRNA decay pathway. Mutations in this gene have been identified in human patients with an autosomal recessive form of intellectual disability. [provided by RefSeq, May 2017]
Gene Name: Enhancer Of MRNA Decapping 3
Chromosome: CHR15: 74922898 -74988386
Locus: 15q24.1
SNX29 Gene Summary
The Sorting Nexin 29 (SNX29) gene is located on chr16 :12070601-12668146 at 16p13.13-p13.12.
Gene Name: Sorting Nexin 29
Chromosome: CHR16: 12070601 -12668146
Locus: 16p13.13-p13.12
Gene Diseases
The EDC3 SNX29 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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