PLEKHA7-USH1C Fusion FISH Probe
The PLEKHA7-USH1C Fusion FISH Probe is used to confirm a fusion of the PLEKHA7 and USH1C genes. The fusion of the PLEKHA7 and USH1C genes has been associated with Esophageal 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. 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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| PLEKHA7-USH1C-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-RERE | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-REOR | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-REGO | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-REGR | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-REAQ | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-ORRE | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-OROR | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-ORGO | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-ORAQ | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-GORE | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-GOOR | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-GOGO | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-GOGR | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-GOAQ | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-GRRE | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-GROR | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-GRGO | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-GRGR | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-GRAQ | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-AQRE | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-AQOR | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-AQGO | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-AQGR | 20 (40 μL) | 200 μL |
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| PLEKHA7-USH1C-20-AQAQ | 20 (40 μL) | 200 μL |
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USH1C Gene Summary
This gene encodes a scaffold protein that functions in the assembly of Usher protein complexes. The protein contains PDZ domains, a coiled-coil region with a bipartite nuclear localization signal and a PEST degradation sequence. Defects in this gene are the cause of Usher syndrome type 1C and non-syndromic sensorineural deafness autosomal recessive type 18. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]
Gene Name: USH1 Protein Network Component Harmonin
Chromosome: CHR11: 17515441 -17565963
Locus: 11p15.1
PLEKHA7 Gene Summary
The Pleckstrin Homology Domain Containing A7 (PLEKHA7) gene is located on chr11 :16809206-17035963 at 11p15.2-p15.1.
Gene Name: Pleckstrin Homology Domain Containing A7
Chromosome: CHR11: 16809206 -17035963
Locus: 11p15.2-p15.1
Gene Diseases
The PLEKHA7 USH1C Fusion has been associated with the following diseases:
| Disease Name |
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| Esophageal Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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