USP9X-BLVRB Fusion FISH Probe
The USP9X-BLVRB Fusion FISH Probe is used to confirm a fusion of the USP9X and BLVRB genes. The fusion of the USP9X and BLVRB genes has been associated with Head And Neck Squamous Cell 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-BLVRB-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-RERE | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-REOR | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-REGO | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-REGR | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-REAQ | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-ORRE | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-OROR | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-ORGO | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-ORAQ | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-GORE | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-GOOR | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-GOGO | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-GOGR | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-GOAQ | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-GRRE | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-GROR | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-GRGO | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-GRGR | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-GRAQ | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-AQRE | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-AQOR | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-AQGO | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-AQGR | 20 (40 μL) | 200 μL |
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| USP9X-BLVRB-20-AQAQ | 20 (40 μL) | 200 μL |
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BLVRB Gene Summary
The final step in heme metabolism in mammals is catalyzed by the cytosolic biliverdin reductase enzymes A and B (EC 1.3.1.24).[supplied by OMIM, Jul 2009]
Gene Name: Biliverdin Reductase B
Chromosome: CHR19: 40953690 -40971725
Locus: 19q13.2
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
Gene Diseases
The USP9X BLVRB Fusion has been associated with the following diseases:
| Disease Name |
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| Head And Neck Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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