RAI1/ERBB2 FISH Probe
Our RAI1/ERBB2 FISH probe is designed to detect ERBB2 amplifications and deletions, with RAI1 serving as a control. The probe comes labeled in green and orange, but can 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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| RAI1-ERBB2-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| RAI1-ERBB2-20-GRRE | 20 (40 μL) | 200 μL |
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| RAI1-ERBB2-20-GRGO | 20 (40 μL) | 200 μL |
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Gene Summary
This gene is located within the Smith-Magenis syndrome region on chromosome 17. It is highly similar to its mouse counterpart and is expressed at high levels mainly in neuronal tissues. The protein encoded by this gene includes a polymorphic polyglutamine tract in the N-terminal domain. Expression of the mouse counterpart in neurons is induced by retinoic acid. This gene is associated with both the severity of the phenotype and the response to medication in schizophrenic patients. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: RAI1
Gene Name: Retinoic Acid Induced 1
Chromosome: CHR17: 17584786-17714765
Locus: 17p11.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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