RBM19-PTPRQ Fusion FISH Probe
The RBM19-PTPRQ Fusion FISH Probe is used to confirm a fusion of the RBM19 and PTPRQ genes. The fusion of the RBM19 and PTPRQ 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. 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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| RBM19-PTPRQ-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-RERE | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-REOR | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-REGO | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-REGR | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-REAQ | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-ORRE | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-OROR | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-ORGO | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-ORAQ | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-GORE | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-GOOR | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-GOGO | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-GOGR | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-GOAQ | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-GRRE | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-GROR | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-GRGO | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-GRGR | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-GRAQ | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-AQRE | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-AQOR | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-AQGO | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-AQGR | 20 (40 μL) | 200 μL |
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| RBM19-PTPRQ-20-AQAQ | 20 (40 μL) | 200 μL |
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RBM19 Gene Summary
This gene encodes a nucleolar protein that contains six RNA-binding motifs. The encoded protein may be involved in regulating ribosome biogenesis. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Apr 2009]
Gene Name: RNA Binding Motif Protein 19
Chromosome: CHR12: 114254542 -114404176
Locus: 12q24.13-q24.21
PTPRQ Gene Summary
This locus encodes a member of the type III receptor-like protein-tyrosine phosphatase family. The encoded protein catalyzes the dephosphorylation of phosphotyrosine and phosphatidylinositol and plays roles in cellular proliferation and differentiation. Mutations at this locus have been linked to autosomal recessive deafness. [provided by RefSeq, Mar 2014]
Gene Name: Protein Tyrosine Phosphatase, Receptor Type Q
Chromosome: CHR12: 80838125 -81073968
Locus: 12q21.31
Gene Diseases
The RBM19 PTPRQ 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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