SLC25A13 Break Apart FISH Probe
Empire Genomics’ SLC25A13 Break Apart FISH Probe is designed to flank the SLC25A13 gene and is typically used for detecting SLC25A13 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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| SLC25A13BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC25A13BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC25A13BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC25A13BA-20-GORE | 20 (40 μL) | 200 μL |
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| SLC25A13BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC25A13BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC25A13BA-20-ORGR | 20 (40 μL) | 200 μL |
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| SLC25A13BA-20-REGO | 20 (40 μL) | 200 μL |
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| SLC25A13BA-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 contains four EF-hand Ca(2+) binding motifs in the N-terminal domain, and localizes to mitochondria. The protein catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in this gene result in citrullinemia, type II. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
Gene Details
Gene Symbol: SLC25A13
Gene Name: Solute Carrier Family 25 Member 13
Chromosome: CHR7: 95749531-95951459
Locus: 7q21.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC25A13 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC25A13-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping