HHH FISH Probe
The HHH FISH probe is designed to hybridize to the HHH gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.
** 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 |
|---|---|---|---|---|
| SLC25A15-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| SLC25A15-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC25A15-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC25A15-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC25A15-20-AQ | 20 (40 μL) | 200 μL |  |
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| SLC25A15-20-DIG | 20 (40 μL) | 200 μL |  |
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| SLC25A15-20-BIO | 20 (40 μL) | 200 μL |  |
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 |
|---|
Customer Publications
Product Details
Product: HHH 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