SNX27-ADAR Fusion FISH Probe
The SNX27-ADAR Fusion FISH Probe is used to confirm a fusion of the SNX27 and ADAR genes. The fusion of the SNX27 and ADAR 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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| SNX27-ADAR-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-RERE | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-REOR | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-REGO | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-REGR | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-REAQ | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-ORRE | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-OROR | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-ORGO | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-ORAQ | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-GORE | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-GOOR | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-GOGO | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-GOGR | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-GOAQ | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-GRRE | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-GROR | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-GRGO | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-GRGR | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-GRAQ | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-AQRE | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-AQOR | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-AQGO | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-AQGR | 20 (40 μL) | 200 μL |
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| SNX27-ADAR-20-AQAQ | 20 (40 μL) | 200 μL |
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ADAR Gene Summary
This gene encodes the enzyme responsible for RNA editing by site-specific deamination of adenosines. This enzyme destabilizes double-stranded RNA through conversion of adenosine to inosine. Mutations in this gene have been associated with dyschromatosis symmetrica hereditaria. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010]
Gene Name: Adenosine Deaminase, RNA Specific
Chromosome: CHR1: 154554533 -154600456
Locus: 1q21.3
SNX27 Gene Summary
This gene encodes a member of the sorting nexin family, a diverse group of cytoplasmic and membrane-associated proteins involved in endocytosis of plasma membrane receptors and protein trafficking through these compartments. All members of this protein family contain a phosphoinositide binding domain (PX domain). A highly similar protein in mouse is responsible for the specific recruitment of an isoform of serotonin 5-hydroxytryptamine 4 receptor into early endosomes, suggesting the analogous role for the human protein. [provided by RefSeq, Jul 2008]
Gene Name: Sorting Nexin Family Member 27
Chromosome: CHR1: 151584661 -151671559
Locus: 1q21.3
Gene Diseases
The SNX27 ADAR 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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