SNX29 Break Apart FISH Probe
Empire Genomics’ SNX29 Break Apart FISH Probe is designed to flank the SNX29 gene and is typically used for detecting SNX29 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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| SNX29BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SNX29BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SNX29BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SNX29BA-20-GORE | 20 (40 μL) | 200 μL |
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| SNX29BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SNX29BA-20-GROR | 20 (40 μL) | 200 μL |
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| SNX29BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SNX29BA-20-REGO | 20 (40 μL) | 200 μL |
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| SNX29BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
The Sorting Nexin 29 (SNX29) gene is located on chr16:12070601 -12668146 at 16p13.13-p13.12.
Gene Details
Gene Symbol: SNX29
Gene Name: Sorting Nexin 29
Chromosome: CHR16: 12070601-12668146
Locus: 16p13.13-p13.12
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SNX29 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SNX29-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping