ERCC8 Break Apart FISH Probe
Empire Genomics’ ERCC8 Break Apart FISH Probe is designed to flank the ERCC8 gene and is typically used for detecting ERCC8 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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| ERCC8BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| ERCC8BA-20-AQOR | 20 (40 μL) | 200 μL |
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| ERCC8BA-20-GOGR | 20 (40 μL) | 200 μL |
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| ERCC8BA-20-GORE | 20 (40 μL) | 200 μL |
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| ERCC8BA-20-GRGO | 20 (40 μL) | 200 μL |
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| ERCC8BA-20-GRRE | 20 (40 μL) | 200 μL |
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| ERCC8BA-20-ORGR | 20 (40 μL) | 200 μL |
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| ERCC8BA-20-REGO | 20 (40 μL) | 200 μL |
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| ERCC8BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014]
Gene Details
Gene Symbol: ERCC8
Gene Name: ERCC Excision Repair 8, CSA Ubiquitin Ligase Complex Subunit
Chromosome: CHR5: 60169658-60240905
Locus: 5q12.1
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: ERCC8 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: ERCC8-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping