TJP2-RPRD2 Fusion FISH Probe
The TJP2-RPRD2 Fusion FISH Probe is used to confirm a fusion of the TJP2 and RPRD2 genes. The fusion of the TJP2 and RPRD2 genes has been associated with Skin Cutaneous Melanoma. 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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| TJP2-RPRD2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-RERE | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-REOR | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-REGO | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-REGR | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-REAQ | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-ORRE | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-OROR | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-ORGO | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-ORAQ | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-GORE | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-GOOR | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-GOGO | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-GOGR | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-GOAQ | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-GRRE | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-GROR | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-GRGO | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-GRGR | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-GRAQ | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-AQRE | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-AQOR | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-AQGO | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-AQGR | 20 (40 μL) | 200 μL |
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| TJP2-RPRD2-20-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
RPRD2 Gene Summary
The Regulation Of Nuclear Pre-mRNA Domain Containing 2 (RPRD2) gene is located on chr1 :150336989-150449041 at 1q21.2.
Gene Name: Regulation Of Nuclear Pre-mRNA Domain Containing 2
Chromosome: CHR1: 150336989 -150449041
Locus: 1q21.2
Gene Diseases
The TJP2 RPRD2 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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