LRFN1-DLL3 Fusion FISH Probe
The LRFN1-DLL3 Fusion FISH Probe is used to confirm a fusion of the LRFN1 and DLL3 genes. The fusion of the LRFN1 and DLL3 genes has been associated with Esophageal 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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| LRFN1-DLL3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-RERE | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-REOR | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-REGO | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-REGR | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-REAQ | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-ORRE | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-OROR | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-ORGO | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-ORAQ | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-GORE | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-GOOR | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-GOGO | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-GOGR | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-GOAQ | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-GRRE | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-GROR | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-GRGO | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-GRGR | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-GRAQ | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-AQRE | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-AQOR | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-AQGO | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-AQGR | 20 (40 μL) | 200 μL |
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| LRFN1-DLL3-20-AQAQ | 20 (40 μL) | 200 μL |
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DLL3 Gene Summary
This gene encodes a member of the delta protein ligand family. This family functions as Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. Mutations in this gene cause autosomal recessive spondylocostal dysostosis 1. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Delta Like Canonical Notch Ligand 3
Chromosome: CHR19: 39989556 -39999121
Locus: 19q13.2
LRFN1 Gene Summary
The Leucine Rich Repeat And Fibronectin Type III Domain Containing 1 (LRFN1) gene is located on chr19 :39797456-39805976 at 19q13.2.
Gene Name: Leucine Rich Repeat And Fibronectin Type III Domain Containing 1
Chromosome: CHR19: 39797456 -39805976
Locus: 19q13.2
Gene Diseases
The LRFN1 DLL3 Fusion has been associated with the following diseases:
| Disease Name |
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| Esophageal Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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