FCHSD2-TPCN2 Fusion FISH Probe
The FCHSD2-TPCN2 Fusion FISH Probe is used to confirm a fusion of the FCHSD2 and TPCN2 genes. The fusion of the FCHSD2 and TPCN2 genes has been associated with 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. 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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| FCHSD2-TPCN2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-RERE | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-REOR | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-REGO | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-REGR | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-REAQ | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-ORRE | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-OROR | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-ORGO | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-ORAQ | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-GORE | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-GOOR | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-GOGO | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-GOGR | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-GOAQ | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-GRRE | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-GROR | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-GRGO | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-GRGR | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-GRAQ | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-AQRE | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-AQOR | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-AQGO | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-AQGR | 20 (40 μL) | 200 μL |
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| FCHSD2-TPCN2-20-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
TPCN2 Gene Summary
This gene encodes a putative cation-selective ion channel with two repeats of a six-transmembrane-domain. The protein localizes to lysosomal membranes and enables nicotinic acid adenine dinucleotide phosphate (NAADP) -induced calcium ion release from lysosome-related stores. This ubiquitously expressed gene has elevated expression in liver and kidney. Two common nonsynonymous SNPs in this gene strongly associate with blond versus brown hair pigmentation.[provided by RefSeq, Dec 2009]
Gene Name: Two Pore Segment Channel 2
Chromosome: CHR11: 68816349 -68858072
Locus: 11q13.3
Gene Diseases
The FCHSD2 TPCN2 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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