KIAA0182-NOTCH3 Fusion FISH Probe
The KIAA0182-NOTCH3 Fusion FISH Probe is used to confirm a fusion of the KIAA0182 and NOTCH3 genes. The fusion of the KIAA0182 and NOTCH3 genes has been associated with Lung Adenocarcinoma. 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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| KIAA0182-NOTCH3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-RERE | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-REOR | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-REGO | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-REGR | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-REAQ | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-ORRE | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-OROR | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-ORGO | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-ORAQ | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-GORE | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-GOOR | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-GOGO | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-GOGR | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-GOAQ | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-GRRE | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-GROR | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-GRGO | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-GRGR | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-GRAQ | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-AQRE | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-AQOR | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-AQGO | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-AQGR | 20 (40 μL) | 200 μL |
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| KIAA0182-NOTCH3-20-AQAQ | 20 (40 μL) | 200 μL |
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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 KIAA0182 NOTCH3 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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