RNASEH2B Break Apart FISH Probe
Empire Genomics’ RNASEH2B Break Apart FISH Probe is designed to flank the RNASEH2B gene and is typically used for detecting RNASEH2B 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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| RNASEH2BBA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| RNASEH2BBA-20-AQOR | 20 (40 μL) | 200 μL |
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| RNASEH2BBA-20-GOGR | 20 (40 μL) | 200 μL |
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| RNASEH2BBA-20-GORE | 20 (40 μL) | 200 μL |
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| RNASEH2BBA-20-GRGO | 20 (40 μL) | 200 μL |
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| RNASEH2BBA-20-GROR | 20 (40 μL) | 200 μL |
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| RNASEH2BBA-20-GRRE | 20 (40 μL) | 200 μL |
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| RNASEH2BBA-20-REGO | 20 (40 μL) | 200 μL |
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| RNASEH2BBA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
RNase H2 is composed of a single catalytic subunit (A) and two non-catalytic subunits (B and C) and specifically degrades the RNA of RNA:DNA hybrids. The protein encoded by this gene is the non-catalytic B subunit of RNase H2, which is thought to play a role in DNA replication. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Aicardi-Goutieres syndrome type 2 (AGS2). [provided by RefSeq, Nov 2008]
Gene Details
Gene Symbol: RNASEH2B
Gene Name: Ribonuclease H2 Subunit B
Chromosome: CHR13: 51483813-51544596
Locus: 13q14.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: RNASEH2B FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: RNASEH2B-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping