NSUN5-BAZ1B Fusion FISH Probe
The NSUN5-BAZ1B Fusion FISH Probe is used to confirm a fusion of the NSUN5 and BAZ1B genes. The fusion of the NSUN5 and BAZ1B genes has been associated with Uterine Corpus Endometrial 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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| NSUN5-BAZ1B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-RERE | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-REOR | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-REGO | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-REGR | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-REAQ | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-ORRE | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-OROR | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-ORGO | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-ORAQ | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-GORE | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-GOOR | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-GOGO | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-GOGR | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-GOAQ | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-GRRE | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-GROR | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-GRGO | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-GRGR | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-GRAQ | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-AQRE | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-AQOR | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-AQGO | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-AQGR | 20 (40 μL) | 200 μL |
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| NSUN5-BAZ1B-20-AQAQ | 20 (40 μL) | 200 μL |
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BAZ1B Gene Summary
This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. [provided by RefSeq, Jul 2008]
Gene Name: Bromodomain Adjacent To Zinc Finger Domain 1B
Chromosome: CHR7: 72854727 -72936615
Locus: 7q11.23
NSUN5 Gene Summary
This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
Gene Name: NOP2/Sun RNA Methyltransferase Family Member 5
Chromosome: CHR7: 72716513 -72722864
Locus: 7q11.23
Gene Diseases
The NSUN5 BAZ1B Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Corpus Endometrial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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