GRHL2-MATN2 Fusion FISH Probe
The GRHL2-MATN2 Fusion FISH Probe is used to confirm a fusion of the GRHL2 and MATN2 genes. The fusion of the GRHL2 and MATN2 genes has been associated with Colon Adenocarcinoma. 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| GRHL2-MATN2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-RERE | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-REOR | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-REGO | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-REGR | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-REAQ | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-ORRE | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-OROR | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-ORGO | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-ORAQ | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-GORE | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-GOOR | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-GOGO | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-GOGR | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-GOAQ | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-GRRE | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-GROR | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-GRGO | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-GRGR | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-GRAQ | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-AQRE | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-AQOR | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-AQGO | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-AQGR | 20 (40 μL) | 200 μL |
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| GRHL2-MATN2-20-AQAQ | 20 (40 μL) | 200 μL |
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MATN2 Gene Summary
This gene encodes a member of the von Willebrand factor A domain containing protein family. This family of proteins is thought to be involved in the formation of filamentous networks in the extracellular matrices of various tissues. This protein contains five von Willebrand factor A domains. The specific function of this gene has not yet been determined. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Matrilin 2
Chromosome: CHR8: 98881310 -99048946
Locus: 8q22.1-q22.2
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 MATN2 Fusion has been associated with the following diseases:
| Disease Name |
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| Colon Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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