SNX16 Break Apart FISH Probe
Empire Genomics’ SNX16 Break Apart FISH Probe is designed to flank the SNX16 gene and is typically used for detecting SNX16 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange 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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| SNX16BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| SNX16BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SNX16BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SNX16BA-20-GORE | 20 (40 μL) | 200 μL |
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| SNX16BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SNX16BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SNX16BA-20-ORGR | 20 (40 μL) | 200 μL |
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| SNX16BA-20-REGO | 20 (40 μL) | 200 μL |
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| SNX16BA-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. The protein encoded by this gene associates with late endosome membranes as is involved in tubule formation, cholesterol transport, and transport of tetraspanin CD81. The encoded protein also inhibits cell migration and tumorigenesis. [provided by RefSeq, Jan 2017]
Gene Details
Gene Symbol: SNX16
Gene Name: Sorting Nexin 16
Chromosome: CHR8: 82711817-82754521
Locus: 8q21.13
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SNX16 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SNX16-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping