GRHL2-TRIM13 Fusion FISH Probe
The GRHL2-TRIM13 Fusion FISH Probe is used to confirm a fusion of the GRHL2 and TRIM13 genes. The fusion of the GRHL2 and TRIM13 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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| GRHL2-TRIM13-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-RERE | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-REOR | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-REGO | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-REGR | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-REAQ | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-ORRE | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-OROR | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-ORGO | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-ORAQ | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-GORE | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-GOOR | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-GOGO | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-GOGR | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-GOAQ | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-GRRE | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-GROR | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-GRGO | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-GRGR | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-GRAQ | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-AQRE | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-AQOR | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-AQGO | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-AQGR | 20 (40 μL) | 200 μL |
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| GRHL2-TRIM13-20-AQAQ | 20 (40 μL) | 200 μL |
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TRIM13 Gene Summary
This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This gene is located on chromosome 13 within the minimal deletion region for B-cell chronic lymphocytic leukemia. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Tripartite Motif Containing 13
Chromosome: CHR13: 50571142 -50592603
Locus: 13q14.2
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 GRHL2 TRIM13 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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