EHHADH Break Apart FISH Probe
Empire Genomics’ EHHADH Break Apart FISH Probe is designed to flank the EHHADH gene and is typically used for detecting EHHADH 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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| EHHADHBA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| EHHADHBA-20-AQOR | 20 (40 μL) | 200 μL |
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| EHHADHBA-20-GOGR | 20 (40 μL) | 200 μL |
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| EHHADHBA-20-GORE | 20 (40 μL) | 200 μL |
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| EHHADHBA-20-GRGO | 20 (40 μL) | 200 μL |
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| EHHADHBA-20-GRRE | 20 (40 μL) | 200 μL |
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| EHHADHBA-20-ORGR | 20 (40 μL) | 200 μL |
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| EHHADHBA-20-REGO | 20 (40 μL) | 200 μL |
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| EHHADHBA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]
Gene Details
Gene Symbol: EHHADH
Gene Name: Enoyl-CoA Hydratase And 3-hydroxyacyl CoA Dehydrogenase
Chromosome: CHR3: 184908411-184971886
Locus: 3q27.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: EHHADH FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: EHHADH-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping