C12ORF52-GRHL2 Fusion FISH Probe
The C12ORF52-GRHL2 Fusion FISH Probe is used to confirm a fusion of the C12ORF52 and GRHL2 genes. The fusion of the C12ORF52 and GRHL2 genes has been associated with Head And Neck Squamous Cell Carcinoma . These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** 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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| C12ORF52-GRHL2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-RERE | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-REOR | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-REGO | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-REGR | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-REAQ | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-ORRE | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-OROR | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-ORGO | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-ORAQ | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-GORE | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-GOOR | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-GOGO | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-GOGR | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-GOAQ | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-GRRE | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-GROR | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-GRGO | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-GRGR | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-GRAQ | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-AQRE | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-AQOR | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-AQGO | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-AQGR | 20 (40 μL) | 200 μL |
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| C12ORF52-GRHL2-20-AQAQ | 20 (40 μL) | 200 μL |
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GRHL2 Gene Summary
The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).[provided by RefSeq, Mar 2009]
Gene Name: Grainyhead Like Transcription Factor 2
Chromosome: CHR8: 102504667 -102681952
Locus: 8q22.3
Gene Diseases
The C12ORF52 GRHL2 Fusion has been associated with the following diseases:
| Disease Name |
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| Head And Neck Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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