SNX9-DAP Fusion FISH Probe
The SNX9-DAP Fusion FISH Probe is used to confirm a fusion of the SNX9 and DAP genes. The fusion of the SNX9 and DAP 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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| SNX9-DAP-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-RERE | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-REOR | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-REGO | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-REGR | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-REAQ | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-ORRE | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-OROR | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-ORGO | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-ORAQ | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-GORE | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-GOOR | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-GOGO | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-GOGR | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-GOAQ | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-GRRE | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-GROR | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-GRGO | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-GRGR | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-GRAQ | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-AQRE | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-AQOR | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-AQGO | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-AQGR | 20 (40 μL) | 200 μL |
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| SNX9-DAP-20-AQAQ | 20 (40 μL) | 200 μL |
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DAP Gene Summary
This gene encodes a basic, proline-rich, 15-kD protein. The protein acts as a positive mediator of programmed cell death that is induced by interferon-gamma. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014]
Gene Name: Death Associated Protein
Chromosome: CHR5: 10679341 -10761387
Locus: 5p15.2
SNX9 Gene Summary
This gene encodes a member of the sorting nexin family. Members of this family contain a phosphoinositide binding domain, and are involved in intracellular trafficking. The encoded protein does not contain a coiled coil region, like some family members, but does contain a SRC homology domain near its N-terminus. The encoded protein is reported to have a variety of interaction partners, including of adaptor protein 2 , dynamin, tyrosine kinase non-receptor 2, Wiskott-Aldrich syndrome-like, and ARP3 actin-related protein 3. The encoded protein is implicated in several stages of intracellular trafficking, including endocytosis, macropinocytosis, and F-actin nucleation. [provided by RefSeq, Jul 2013]
Gene Name: Sorting Nexin 9
Chromosome: CHR6: 158244293 -158366109
Locus: 6q25.3
Gene Diseases
The SNX9 DAP 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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