GRHL2-C10ORF58 Fusion FISH Probe
The GRHL2-C10ORF58 Fusion FISH Probe is used to confirm a fusion of the GRHL2 and C10ORF58 genes. The fusion of the GRHL2 and C10ORF58 genes has been associated with Breast Invasive 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-C10ORF58-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-RERE | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-REOR | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-REGO | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-REGR | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-REAQ | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-ORRE | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-OROR | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-ORGO | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-ORAQ | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-GORE | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-GOOR | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-GOGO | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-GOGR | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-GOAQ | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-GRRE | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-GROR | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-GRGO | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-GRGR | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-GRAQ | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-AQRE | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-AQOR | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-AQGO | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-AQGR | 20 (40 μL) | 200 μL | ||
GRHL2-C10ORF58-20-AQAQ | 20 (40 μL) | 200 μL |
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 C10ORF58 Fusion has been associated with the following diseases:
Disease Name |
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Breast Invasive Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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