SNX17 Break Apart FISH Probe
Empire Genomics’ SNX17 Break Apart FISH Probe is designed to flank the SNX17 gene and is typically used for detecting SNX17 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green by default, but may be customized to meet your needs.
** 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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| SNX17BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SNX17BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SNX17BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SNX17BA-20-GORE | 20 (40 μL) | 200 μL |
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| SNX17BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SNX17BA-20-GROR | 20 (40 μL) | 200 μL |
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| SNX17BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SNX17BA-20-REGO | 20 (40 μL) | 200 μL |
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| SNX17BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members, but contains a B41 domain. This protein interacts with the cytoplasmic domain of P-selectin, and may function in the intracellular trafficking of P-selectin. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2012]
Gene Details
Gene Symbol: SNX17
Gene Name: Sorting Nexin 17
Chromosome: CHR2: 27593388-27599994
Locus: 2p23.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SNX17 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SNX17-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping