ATP5H-HN1 Fusion FISH Probe
The ATP5H-HN1 Fusion FISH Probe is used to confirm a fusion of the ATP5H and HN1 genes. The fusion of the ATP5H and HN1 genes has been associated with Bladder Urothelial 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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| ATP5H-HN1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-RERE | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-REOR | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-REGO | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-REGR | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-REAQ | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-ORRE | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-OROR | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-ORGO | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-ORAQ | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-GORE | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-GOOR | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-GOGO | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-GOGR | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-GOAQ | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-GRRE | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-GROR | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-GRGO | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-GRGR | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-GRAQ | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-AQRE | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-AQOR | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-AQGO | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-AQGR | 20 (40 μL) | 200 μL |
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| ATP5H-HN1-20-AQAQ | 20 (40 μL) | 200 μL |
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ATP5H Gene Summary
Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the d subunit of the Fo complex. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. In addition, three pseudogenes are located on chromosomes 9, 12 and 15. [provided by RefSeq, Jun 2010]
Gene Name: ATP Synthase, H+ Transporting, Mitochondrial Fo Complex Subunit D
Chromosome: CHR17: 73034954 -73043074
Locus: 17q25.1
Gene Diseases
The ATP5H HN1 Fusion has been associated with the following diseases:
| Disease Name |
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| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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