PDSS1 Break Apart FISH Probe
Empire Genomics’ PDSS1 Break Apart FISH Probe is designed to flank the PDSS1 gene and is typically used for detecting PDSS1 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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PDSS1BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
PDSS1BA-20-AQOR | 20 (40 μL) | 200 μL | ||
PDSS1BA-20-GOGR | 20 (40 μL) | 200 μL | ||
PDSS1BA-20-GORE | 20 (40 μL) | 200 μL | ||
PDSS1BA-20-GRGO | 20 (40 μL) | 200 μL | ||
PDSS1BA-20-GROR | 20 (40 μL) | 200 μL | ||
PDSS1BA-20-GRRE | 20 (40 μL) | 200 μL | ||
PDSS1BA-20-REGO | 20 (40 μL) | 200 μL | ||
PDSS1BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
The protein encoded by this gene is an enzyme that elongates the prenyl side-chain of coenzyme Q, or ubiquinone, one of the key elements in the respiratory chain. The gene product catalyzes the formation of all trans-polyprenyl pyrophosphates from isopentyl diphosphate in the assembly of polyisoprenoid side chains, the first step in coenzyme Q biosynthesis. The protein may be peripherally associated with the inner mitochondrial membrane, though no transit peptide has been definitively identified to date. Defects in this gene are a cause of coenzyme Q10 deficiency. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: PDSS1
Gene Name: Decaprenyl Diphosphate Synthase Subunit 1
Chromosome: CHR10: 26986594-27035726
Locus: 10p12.1
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: PDSS1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: PDSS1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping