RBM39-OCA2 Fusion FISH Probe
The RBM39-OCA2 Fusion FISH Probe is used to confirm a fusion of the RBM39 and OCA2 genes. The fusion of the RBM39 and OCA2 genes has been associated with Sarcoma. 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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| RBM39-OCA2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-RERE | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-REOR | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-REGO | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-REGR | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-REAQ | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-ORRE | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-OROR | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-ORGO | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-ORAQ | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-GORE | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-GOOR | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-GOGO | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-GOGR | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-GOAQ | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-GRRE | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-GROR | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-GRGO | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-GRGR | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-GRAQ | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-AQRE | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-AQOR | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-AQGO | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-AQGR | 20 (40 μL) | 200 μL |
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| RBM39-OCA2-20-AQAQ | 20 (40 μL) | 200 μL |
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OCA2 Gene Summary
This gene encodes the human homolog of the mouse p (pink-eyed dilution) gene. The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine, which is a precursor to melanin synthesis. It is involved in mammalian pigmentation, where it may control skin color variation and act as a determinant of brown or blue eye color. Mutations in this gene result in type 2 oculocutaneous albinism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]
Gene Name: OCA2 Melanosomal Transmembrane Protein
Chromosome: CHR15: 28000022 -28344458
Locus: 15q12-q13.1
RBM39 Gene Summary
This gene encodes a member of the U2AF65 family of proteins. The encoded protein is found in the nucleus, where it co-localizes with core spliceosomal proteins. It has been shown to play a role in both steroid hormone receptor-mediated transcription and alternative splicing, and it is also a transcriptional coregulator of the viral oncoprotein v-Rel. Multiple transcript variants have been observed for this gene. A related pseudogene has been identified on chromosome X. [provided by RefSeq, Aug 2011]
Gene Name: RNA Binding Motif Protein 39
Chromosome: CHR20: 34291530 -34330258
Locus: 20q11.22
Gene Diseases
The RBM39 OCA2 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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