FCHSD2-ATP6V1H Fusion FISH Probe
The FCHSD2-ATP6V1H Fusion FISH Probe is used to confirm a fusion of the FCHSD2 and ATP6V1H genes. The fusion of the FCHSD2 and ATP6V1H genes has been associated with Skin Cutaneous Melanoma, and Skin Cutaneous Melanoma. 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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| FCHSD2-ATP6V1H-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-RERE | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-REOR | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-REGO | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-REGR | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-REAQ | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-ORRE | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-OROR | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-ORGO | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-ORAQ | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-GORE | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-GOOR | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-GOGO | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-GOGR | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-GOAQ | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-GRRE | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-GROR | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-GRGO | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-GRGR | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-GRAQ | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-AQRE | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-AQOR | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-AQGO | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-AQGR | 20 (40 μL) | 200 μL |
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| FCHSD2-ATP6V1H-20-AQAQ | 20 (40 μL) | 200 μL |
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FCHSD2 Gene Summary
The FCH And Double SH3 Domains 2 (FCHSD2) gene is located on chr11 :72547789-72853143 at 11q13.4.
Gene Name: FCH And Double SH3 Domains 2
Chromosome: CHR11: 72547789 -72853143
Locus: 11q13.4
ATP6V1H Gene Summary
This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular organelles. V-ATPase-dependent organelle acidification is necessary for multiple processes including protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. The encoded protein is the regulatory H subunit of the V1 domain of V-ATPase, which is required for catalysis of ATP but not the assembly of V-ATPase. Decreased expression of this gene may play a role in the development of type 2 diabetes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]
Gene Name: ATPase H+ Transporting V1 Subunit H
Chromosome: CHR8: 54628114 -54755850
Locus: 8q11.23
Gene Diseases
The FCHSD2 ATP6V1H Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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