HK1-CTNNA3 Fusion FISH Probe
The HK1-CTNNA3 Fusion FISH Probe is used to confirm a fusion of the HK1 and CTNNA3 genes. The fusion of the HK1 and CTNNA3 genes has been associated with Prostate Adenocarcinoma. 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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| HK1-CTNNA3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-RERE | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-REOR | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-REGO | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-REGR | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-REAQ | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-ORRE | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-OROR | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-ORGO | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-ORAQ | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-GORE | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-GOOR | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-GOGO | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-GOGR | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-GOAQ | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-GRRE | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-GROR | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-GRGO | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-GRGR | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-GRAQ | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-AQRE | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-AQOR | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-AQGO | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-AQGR | 20 (40 μL) | 200 μL |
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| HK1-CTNNA3-20-AQAQ | 20 (40 μL) | 200 μL |
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HK1 Gene Summary
Hexokinases phosphorylate glucose to produce glucose-6-phosphate, the first step in most glucose metabolism pathways. This gene encodes a ubiquitous form of hexokinase which localizes to the outer membrane of mitochondria. Mutations in this gene have been associated with hemolytic anemia due to hexokinase deficiency. Alternative splicing of this gene results in several transcript variants which encode different isoforms, some of which are tissue-specific. [provided by RefSeq, Apr 2016]
Gene Name: Hexokinase 1
Chromosome: CHR10: 71029755 -71161637
Locus: 10q22.1
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 HK1 CTNNA3 Fusion has been associated with the following diseases:
| Disease Name |
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| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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