RNGTT-AHI1 Fusion FISH Probe
The RNGTT-AHI1 Fusion FISH Probe is used to confirm a fusion of the RNGTT and AHI1 genes. The fusion of the RNGTT and AHI1 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. 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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RNGTT-AHI1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-RERE | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-REOR | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-REGO | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-REGR | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-REAQ | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-ORRE | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-OROR | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-ORGO | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-ORAQ | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-GORE | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-GOOR | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-GOGO | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-GOGR | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-GOAQ | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-GRRE | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-GROR | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-GRGO | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-GRGR | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-GRAQ | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-AQRE | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-AQOR | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-AQGO | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-AQGR | 20 (40 μL) | 200 μL | ||
RNGTT-AHI1-20-AQAQ | 20 (40 μL) | 200 μL |
RNGTT Gene Summary
The RNA Guanylyltransferase And 5'-phosphatase (RNGTT) gene is located on chr6 :89319988-89673348 at 6q15.
Gene Name: RNA Guanylyltransferase And 5'-phosphatase
Chromosome: CHR6: 89319988 -89673348
Locus: 6q15
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
Gene Diseases
The RNGTT AHI1 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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