BAZ1B-BCL7B Fusion FISH Probe
The BAZ1B-BCL7B Fusion FISH Probe is used to confirm a fusion of the BAZ1B and BCL7B genes. The fusion of the BAZ1B and BCL7B genes has been associated with Liver Hepatocellular 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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| BAZ1B-BCL7B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-RERE | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-REOR | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-REGO | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-REGR | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-REAQ | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-ORRE | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-OROR | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-ORGO | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-ORAQ | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-GORE | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-GOOR | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-GOGO | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-GOGR | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-GOAQ | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-GRRE | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-GROR | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-GRGO | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-GRGR | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-GRAQ | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-AQRE | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-AQOR | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-AQGO | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-20-AQGR | 20 (40 μL) | 200 μL |
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| BAZ1B-BCL7B-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
BCL7B Gene Summary
This gene encodes a member of the BCL7 family including BCL7A, BCL7B and BCL7C proteins. This member is BCL7B, which contains a region that is highly similar to the N-terminal segment of BCL7A or BCL7C proteins. The BCL7A protein is encoded by the gene known to be directly involved in a three-way gene translocation in a Burkitt lymphoma cell line. This gene is located at a chromosomal region commonly deleted in Williams syndrome. This gene is highly conserved from C. elegans to human. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Oct 2010]
Gene Name: BCL Tumor Suppressor 7B
Chromosome: CHR7: 72950682 -72972065
Locus: 7q11.23
Gene Diseases
The BAZ1B BCL7B Fusion has been associated with the following diseases:
| Disease Name |
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| Liver Hepatocellular Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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