BAP1-PBRM1 Fusion FISH Probe
The BAP1-PBRM1 Fusion FISH Probe is used to confirm a fusion of the BAP1 and PBRM1 genes. The fusion of the BAP1 and PBRM1 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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| BAP1-PBRM1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-RERE | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-REOR | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-REGO | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-REGR | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-REAQ | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-ORRE | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-OROR | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-ORGO | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-ORAQ | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-GORE | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-GOOR | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-GOGO | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-GOGR | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-GOAQ | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-GRRE | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-GROR | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-GRGO | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-GRGR | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-GRAQ | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-AQRE | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-AQOR | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-AQGO | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-AQGR | 20 (40 μL) | 200 μL |
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| BAP1-PBRM1-20-AQAQ | 20 (40 μL) | 200 μL |
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BAP1 Gene Summary
This gene belongs to the ubiquitin C-terminal hydrolase subfamily of deubiquitinating enzymes that are involved in the removal of ubiquitin from proteins. The encoded enzyme binds to the breast cancer type 1 susceptibility protein (BRCA1) via the RING finger domain of the latter and acts as a tumor suppressor. In addition, the enzyme may be involved in regulation of transcription, regulation of cell cycle and growth, response to DNA damage and chromatin dynamics. Germline mutations in this gene may be associated with tumor predisposition syndrome (TPDS), which involves increased risk of cancers including malignant mesothelioma, uveal melanoma and cutaneous melanoma. [provided by RefSeq, May 2013]
Gene Name: BRCA1 Associated Protein 1
Chromosome: CHR3: 52435024 -52444009
Locus: 3p21.1
PBRM1 Gene Summary
This locus encodes a subunit of ATP-dependent chromatin-remodeling complexes. The encoded protein has been identified as in integral component of complexes necessary for ligand-dependent transcriptional activation by nuclear hormone receptors. Mutations at this locus have been associated with primary clear cell renal cell carcinoma. [provided by RefSeq, Feb 2012]
Gene Name: Polybromo 1
Chromosome: CHR3: 52579367 -52719866
Locus: 3p21.1
Gene Diseases
The BAP1 PBRM1 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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