RNASEH2C Break Apart FISH Probe
Empire Genomics’ RNASEH2C Break Apart FISH Probe is designed to flank the RNASEH2C gene and is typically used for detecting RNASEH2C 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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| RNASEH2CBA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| RNASEH2CBA-20-AQOR | 20 (40 μL) | 200 μL |
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| RNASEH2CBA-20-GOGR | 20 (40 μL) | 200 μL |
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| RNASEH2CBA-20-GORE | 20 (40 μL) | 200 μL |
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| RNASEH2CBA-20-GRGO | 20 (40 μL) | 200 μL |
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| RNASEH2CBA-20-GRRE | 20 (40 μL) | 200 μL |
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| RNASEH2CBA-20-ORGR | 20 (40 μL) | 200 μL |
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| RNASEH2CBA-20-REGO | 20 (40 μL) | 200 μL |
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| RNASEH2CBA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a ribonuclease H subunit that can cleave ribonucleotides from RNA:DNA duplexes. Mutations in this gene cause Aicardi-Goutieres syndrome-3, a disease that causes severe neurologic dysfunction. A pseudogene for this gene has been identified on chromosome Y, near the sex determining region Y (SRY) gene. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: RNASEH2C
Gene Name: Ribonuclease H2 Subunit C
Chromosome: CHR11: 65485143-65488409
Locus: 11q13.1
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: RNASEH2C FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: RNASEH2C-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping