SLC25A12 Break Apart FISH Probe
Empire Genomics’ SLC25A12 Break Apart FISH Probe is designed to flank the SLC25A12 gene and is typically used for detecting SLC25A12 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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| SLC25A12BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC25A12BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC25A12BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC25A12BA-20-GORE | 20 (40 μL) | 200 μL |
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| SLC25A12BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC25A12BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC25A12BA-20-ORGR | 20 (40 μL) | 200 μL |
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| SLC25A12BA-20-REGO | 20 (40 μL) | 200 μL |
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| SLC25A12BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a calcium-binding mitochondrial carrier protein. The encoded protein localizes to the mitochondria and is involved in the exchange of aspartate for glutamate across the inner mitochondrial membrane. Polymorphisms in this gene may be associated with autism, and mutations in this gene may also be a cause of global cerebral hypomyelination. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Apr 2012]
Gene Details
Gene Symbol: SLC25A12
Gene Name: Solute Carrier Family 25 Member 12
Chromosome: CHR2: 172639914-172750813
Locus: 2q31.1
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC25A12 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC25A12-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping