TJP2-STX17 Fusion FISH Probe
The TJP2-STX17 Fusion FISH Probe is used to confirm a fusion of the TJP2 and STX17 genes. The fusion of the TJP2 and STX17 genes has been associated with Lung Squamous Cell 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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| TJP2-STX17-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-RERE | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-REOR | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-REGO | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-REGR | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-REAQ | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-ORRE | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-OROR | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-ORGO | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-ORAQ | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-GORE | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-GOOR | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-GOGO | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-GOGR | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-GOAQ | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-GRRE | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-GROR | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-GRGO | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-GRGR | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-GRAQ | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-AQRE | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-AQOR | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-AQGO | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-AQGR | 20 (40 μL) | 200 μL |
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| TJP2-STX17-20-AQAQ | 20 (40 μL) | 200 μL |
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TJP2 Gene Summary
This gene encodes a zonula occluden that is a member of the membrane-associated guanylate kinase homolog family. The encoded protein functions as a component of the tight junction barrier in epithelial and endothelial cells and is necessary for proper assembly of tight junctions. Mutations in this gene have been identified in patients with hypercholanemia, and genomic duplication of a 270 kb region including this gene causes autosomal dominant deafness-51. Alternatively spliced transcripts encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]
Gene Name: Tight Junction Protein 2
Chromosome: CHR9: 71736223 -71870124
Locus: 9q21.11
STX17 Gene Summary
The Syntaxin 17 (STX17) gene is located on chr9 :102668914-102736818 at 9q31.1.
Gene Name: Syntaxin 17
Chromosome: CHR9: 102668914 -102736818
Locus: 9q31.1
Gene Diseases
The TJP2 STX17 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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