AHI1-C12ORF50 Fusion FISH Probe
The AHI1-C12ORF50 Fusion FISH Probe is used to confirm a fusion of the AHI1 and C12ORF50 genes. The fusion of the AHI1 and C12ORF50 genes has been associated with Skin Cutaneous Melanoma. 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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| AHI1-C12ORF50-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-RERE | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-REOR | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-REGO | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-REGR | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-REAQ | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-ORRE | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-OROR | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-ORGO | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-ORAQ | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-GORE | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-GOOR | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-GOGO | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-GOGR | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-GOAQ | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-GRRE | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-GROR | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-GRGO | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-GRGR | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-GRAQ | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-AQRE | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-AQOR | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-AQGO | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-AQGR | 20 (40 μL) | 200 μL |
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| AHI1-C12ORF50-20-AQAQ | 20 (40 μL) | 200 μL |
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AHI1 Gene Summary
This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]
Gene Name: Abelson Helper Integration Site 1
Chromosome: CHR6: 135605109 -135818903
Locus: 6q23.3
C12orf50 Gene Summary
The Chromosome 12 Open Reading Frame 50 (C12orf50) gene is located on chr12 :88373815-88423176 at 12q21.32.
Gene Name: Chromosome 12 Open Reading Frame 50
Chromosome: CHR12: 88373815 -88423176
Locus: 12q21.32
Gene Diseases
The AHI1 C12ORF50 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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