USP9X-ATP6AP2 Fusion FISH Probe
The USP9X-ATP6AP2 Fusion FISH Probe is used to confirm a fusion of the USP9X and ATP6AP2 genes. The fusion of the USP9X and ATP6AP2 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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| USP9X-ATP6AP2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-RERE | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-REOR | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-REGO | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-REGR | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-REAQ | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-ORRE | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-OROR | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-ORGO | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-ORAQ | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-GORE | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-GOOR | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-GOGO | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-GOGR | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-GOAQ | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-GRRE | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-GROR | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-GRGO | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-GRGR | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-GRAQ | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-AQRE | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-AQOR | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-AQGO | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-AQGR | 20 (40 μL) | 200 μL |
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| USP9X-ATP6AP2-20-AQAQ | 20 (40 μL) | 200 μL |
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USP9X Gene Summary
This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
Gene Name: Ubiquitin Specific Peptidase 9, X-linked
Chromosome: CHRX: 40944887 -41095832
Locus: Xp11.4
ATP6AP2 Gene Summary
This gene encodes a protein that is associated with adenosine triphosphatases (ATPases). Proton-translocating ATPases have fundamental roles in energy conservation, secondary active transport, acidification of intracellular compartments, and cellular pH homeostasis. There are three classes of ATPases- F, P, and V. The vacuolar (V-type) ATPases have a transmembrane proton-conducting sector and an extramembrane catalytic sector. The encoded protein has been found associated with the transmembrane sector of the V-type ATPases. [provided by RefSeq, Jul 2008]
Gene Name: ATPase H+ Transporting Accessory Protein 2
Chromosome: CHRX: 40440215 -40465888
Locus: Xp11.4
Gene Diseases
The USP9X ATP6AP2 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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