NOTCH3-CACNA1A Fusion FISH Probe
The NOTCH3-CACNA1A Fusion FISH Probe is used to confirm a fusion of the NOTCH3 and CACNA1A genes. The fusion of the NOTCH3 and CACNA1A genes has been associated with Sarcoma. 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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| NOTCH3-CACNA1A-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-RERE | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-REOR | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-REGO | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-REGR | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-REAQ | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-ORRE | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-OROR | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-ORGO | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-ORAQ | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-GORE | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-GOOR | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-GOGO | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-GOGR | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-GOAQ | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-GRRE | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-GROR | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-GRGO | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-GRGR | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-GRAQ | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-AQRE | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-AQOR | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-AQGO | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-AQGR | 20 (40 μL) | 200 μL |
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| NOTCH3-CACNA1A-20-AQAQ | 20 (40 μL) | 200 μL |
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CACNA1A Gene Summary
Voltage-dependent calcium channels mediate the entry of calcium ions into excitable cells, and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, and gene expression. Calcium channels are multisubunit complexes composed of alpha-1, beta, alpha-2/delta, and gamma subunits. The channel activity is directed by the pore-forming alpha-1 subunit, whereas, the others act as auxiliary subunits regulating this activity. The distinctive properties of the calcium channel types are related primarily to the expression of a variety of alpha-1 isoforms, alpha-1A, B, C, D, E, and S. This gene encodes the alpha-1A subunit, which is predominantly expressed in neuronal tissue. Mutations in this gene are associated with 2 neurologic disorders, familial hemiplegic migraine and episodic ataxia 2. This gene also exhibits polymorphic variation due to (CAG)n-repeats. Multiple transcript variants encoding different isoforms have been found for this gene. In one set of transcript variants, the (CAG)n-repeats occur in the 3' UTR, and are not associated with any disease. But in another set of variants, an insertion extends the coding region to include the (CAG)n-repeats which encode a polyglutamine tract. Expansion of the (CAG)n-repeats from the normal 4-18 to 21-33 in the coding region is associated with spinocerebellar ataxia 6. [provided by RefSeq, Jul 2016]
Gene Name: Calcium Voltage-gated Channel Subunit Alpha1 A
Chromosome: CHR19: 13317255 -13617274
Locus: 19p13.13
NOTCH3 Gene Summary
This gene encodes the third discovered human homologue of the Drosophilia melanogaster type I membrane protein notch. In Drosophilia, notch interaction with its cell-bound ligands (delta, serrate) establishes an intercellular signalling pathway that plays a key role in neural development. Homologues of the notch-ligands have also been identified in human, but precise interactions between these ligands and the human notch homologues remains to be determined. Mutations in NOTCH3 have been identified as the underlying cause of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). [provided by RefSeq, Jul 2008]
Gene Name: Notch 3
Chromosome: CHR19: 15270443 -15311792
Locus: 19p13.12
Gene Diseases
The NOTCH3 CACNA1A Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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