PBX1-CTNNA3 Fusion FISH Probe
The PBX1-CTNNA3 Fusion FISH Probe is used to confirm a fusion of the PBX1 and CTNNA3 genes. The fusion of the PBX1 and CTNNA3 genes has been associated with Breast Invasive 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| PBX1-CTNNA3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-RERE | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-REOR | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-REGO | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-REGR | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-REAQ | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-ORRE | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-OROR | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-ORGO | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-ORAQ | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-GORE | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-GOOR | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-GOGO | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-GOGR | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-GOAQ | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-GRRE | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-GROR | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-GRGO | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-GRGR | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-GRAQ | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-AQRE | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-AQOR | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-AQGO | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-AQGR | 20 (40 μL) | 200 μL |
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| PBX1-CTNNA3-20-AQAQ | 20 (40 μL) | 200 μL |
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PBX1 Gene Summary
This gene encodes a nuclear protein that belongs to the PBX homeobox family of transcriptional factors. Studies in mice suggest that this gene may be involved in the regulation of osteogenesis and required for skeletal patterning and programming. A chromosomal translocation, t(1;19) involving this gene and TCF3/E2A gene, is associated with pre-B-cell acute lymphoblastic leukemia. The resulting fusion protein, in which the DNA binding domain of E2A is replaced by the DNA binding domain of this protein, transforms cells by constitutively activating transcription of genes regulated by the PBX protein family. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2017]
Gene Name: PBX Homeobox 1
Chromosome: CHR1: 164528596 -164821060
Locus: 1q23.3
CTNNA3 Gene Summary
This gene encodes a protein that belongs to the vinculin/alpha-catenin family. The encoded protein plays a role in cell-cell adhesion in muscle cells. Mutations in this gene are associated with arrhythmogenic right ventricular dysplasia, familial 13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]
Gene Name: Catenin Alpha 3
Chromosome: CHR10: 67679724 -69455949
Locus: 10q21.3
Gene Diseases
The PBX1 CTNNA3 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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