RCAN1-GART Fusion FISH Probe
The RCAN1-GART Fusion FISH Probe is used to confirm a fusion of the RCAN1 and GART genes. The fusion of the RCAN1 and GART 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. 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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RCAN1-GART-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-RERE | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-REOR | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-REGO | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-REGR | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-REAQ | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-ORRE | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-OROR | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-ORGO | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-ORAQ | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-GORE | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-GOOR | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-GOGO | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-GOGR | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-GOAQ | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-GRRE | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-GROR | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-GRGO | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-GRGR | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-GRAQ | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-AQRE | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-AQOR | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-AQGO | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-AQGR | 20 (40 μL) | 200 μL | ||
RCAN1-GART-20-AQAQ | 20 (40 μL) | 200 μL |
RCAN1 Gene Summary
The protein encoded by this gene interacts with calcineurin A and inhibits calcineurin-dependent signaling pathways, possibly affecting central nervous system development. This gene is located in the minimal candidate region for the Down syndrome phenotype, and is overexpressed in the brain of Down syndrome fetuses. Chronic overexpression of this gene may lead to neurofibrillary tangles such as those associated with Alzheimer disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]
Gene Name: Regulator Of Calcineurin 1
Chromosome: CHR21: 35888783 -35987382
Locus: 21q22.12
GART Gene Summary
The protein encoded by this gene is a trifunctional polypeptide. It has phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase activity which is required for de novo purine biosynthesis. This enzyme is highly conserved in vertebrates. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Gene Name: Phosphoribosylglycinamide Formyltransferase, Phosphoribosylglycinamide Synthetase, Phosphoribosylaminoimidazole Synthetase
Chromosome: CHR21: 34876237 -34915198
Locus: 21q22.11
Gene Diseases
The RCAN1 GART 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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