SLC25A15 Break Apart FISH Probe
Empire Genomics’ SLC25A15 Break Apart FISH Probe is designed to flank the SLC25A15 gene and is typically used for detecting SLC25A15 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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| SLC25A15BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC25A15BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC25A15BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC25A15BA-20-GORE | 20 (40 μL) | 200 μL |
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| SLC25A15BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC25A15BA-20-GROR | 20 (40 μL) | 200 μL |
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| SLC25A15BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC25A15BA-20-REGO | 20 (40 μL) | 200 μL |
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| SLC25A15BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene is a member of the mitochondrial carrier family. The encoded protein transports ornithine across the inner mitochondrial membrane from the cytosol to the mitochondrial matrix. The protein is an essential component of the urea cycle, and functions in ammonium detoxification and biosynthesis of the amino acid arginine. Mutations in this gene result in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. There is a pseudogene of this locus on the Y chromosome.[provided by RefSeq, May 2009]
Gene Details
Gene Symbol: SLC25A15
Gene Name: Solute Carrier Family 25 Member 15
Chromosome: CHR13: 41363546-41386596
Locus: 13q14.11
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC25A15 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC25A15-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping