SLC25A4 Break Apart FISH Probe
Empire Genomics’ SLC25A4 Break Apart FISH Probe is designed to flank the SLC25A4 gene and is typically used for detecting SLC25A4 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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| SLC25A4BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC25A4BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC25A4BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC25A4BA-20-GORE | 20 (40 μL) | 200 μL |
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| SLC25A4BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC25A4BA-20-GROR | 20 (40 μL) | 200 μL |
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| SLC25A4BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC25A4BA-20-REGO | 20 (40 μL) | 200 μL |
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| SLC25A4BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy. [provided by RefSeq, Jun 2013]
Gene Details
Gene Symbol: SLC25A4
Gene Name: Solute Carrier Family 25 Member 4
Chromosome: CHR4: 186064416-186071538
Locus: 4q35.1
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC25A4 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC25A4-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping