PHYH Break Apart FISH Probe
Empire Genomics’ PHYH Break Apart FISH Probe is designed to flank the PHYH gene and is typically used for detecting PHYH 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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| PHYHBA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| PHYHBA-20-AQOR | 20 (40 μL) | 200 μL |
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| PHYHBA-20-GOGR | 20 (40 μL) | 200 μL |
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| PHYHBA-20-GORE | 20 (40 μL) | 200 μL |
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| PHYHBA-20-GRGO | 20 (40 μL) | 200 μL |
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| PHYHBA-20-GRRE | 20 (40 μL) | 200 μL |
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| PHYHBA-20-ORGR | 20 (40 μL) | 200 μL |
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| PHYHBA-20-REGO | 20 (40 μL) | 200 μL |
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| PHYHBA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene is a member of the PhyH family and encodes a peroxisomal protein that is involved in the alpha-oxidation of 3-methyl branched fatty acids. Specifically, this protein converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. Mutations in this gene have been associated with Refsum disease (RD) and deficient protein activity has been associated with Zellweger syndrome and rhizomelic chondrodysplasia punctata. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: PHYH
Gene Name: Phytanoyl-CoA 2-hydroxylase
Chromosome: CHR10: 13319795-13342130
Locus: 10p13
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: PHYH FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: PHYH-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping