USP9X-ZNF692 Fusion FISH Probe
The USP9X-ZNF692 Fusion FISH Probe is used to confirm a fusion of the USP9X and ZNF692 genes. The fusion of the USP9X and ZNF692 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| USP9X-ZNF692-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-RERE | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-REOR | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-REGO | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-REGR | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-REAQ | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-ORRE | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-OROR | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-ORGO | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-ORAQ | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-GORE | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-GOOR | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-GOGO | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-GOGR | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-GOAQ | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-GRRE | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-GROR | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-GRGO | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-GRGR | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-GRAQ | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-AQRE | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-AQOR | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-AQGO | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-AQGR | 20 (40 μL) | 200 μL |
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| USP9X-ZNF692-20-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
ZNF692 Gene Summary
The Zinc Finger Protein 692 (ZNF692) gene is located on chr1 :249144202-249153315 at 1q44.
Gene Name: Zinc Finger Protein 692
Chromosome: CHR1: 249144202 -249153315
Locus: 1q44
Gene Diseases
The USP9X ZNF692 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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