SUCLA2 Break Apart FISH Probe
Empire Genomics’ SUCLA2 Break Apart FISH Probe is designed to flank the SUCLA2 gene and is typically used for detecting SUCLA2 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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| SUCLA2BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| SUCLA2BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SUCLA2BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SUCLA2BA-20-GORE | 20 (40 μL) | 200 μL |
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| SUCLA2BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SUCLA2BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SUCLA2BA-20-ORGR | 20 (40 μL) | 200 μL |
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| SUCLA2BA-20-REGO | 20 (40 μL) | 200 μL |
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| SUCLA2BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
Succinyl-CoA synthetase (SCS) is a mitochondrial matrix enzyme that acts as a heterodimer, being composed of an invariant alpha subunit and a substrate-specific beta subunit. The protein encoded by this gene is an ATP-specific SCS beta subunit that dimerizes with the SCS alpha subunit to form SCS-A, an essential component of the tricarboxylic acid cycle. SCS-A hydrolyzes ATP to convert succinate to succinyl-CoA. Defects in this gene are a cause of myopathic mitochondrial DNA depletion syndrome. A pseudogene of this gene has been found on chromosome 6. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: SUCLA2
Gene Name: Succinate-CoA Ligase ADP-forming Beta Subunit
Chromosome: CHR13: 48516790-48575462
Locus: 13q14.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SUCLA2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SUCLA2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping