SULT4A1-TFIP11 Fusion FISH Probe
The SULT4A1-TFIP11 Fusion FISH Probe is used to confirm a fusion of the SULT4A1 and TFIP11 genes. The fusion of the SULT4A1 and TFIP11 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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| SULT4A1-TFIP11-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-RERE | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-REOR | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-REGO | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-REGR | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-REAQ | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-ORRE | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-OROR | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-ORGO | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-ORAQ | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-GORE | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-GOOR | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-GOGO | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-GOGR | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-GOAQ | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-GRRE | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-GROR | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-GRGO | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-GRGR | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-GRAQ | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-AQRE | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-AQOR | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-AQGO | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-AQGR | 20 (40 μL) | 200 μL |
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| SULT4A1-TFIP11-20-AQAQ | 20 (40 μL) | 200 μL |
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TFIP11 Gene Summary
This gene encodes a protein component of the spliceosome that promotes the release of the lariat-intron during late-stage splicing through the recruitment of a pre-mRNA splicing factor called DEAH-box helicase 15. The encoded protein contains a G-patch domain, a hallmark of RNA-processing proteins, that binds DEAH-box helicase 15. This protein contains an atypical nuclear localization sequence as well as a nuclear speckle-targeting sequence, enabling it to localize to distinct speckled regions within the cell nucleus. Polymorphisms in this gene are associated with dental caries suggesting a role in amelogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]
Gene Name: Tuftelin Interacting Protein 11
Chromosome: CHR22: 26887893 -26908437
Locus: 22q12.1
SULT4A1 Gene Summary
This gene encodes a member of the sulfotransferase family. The encoded protein is a brain-specific sulfotransferase believed to be involved in the metabolism of neurotransmitters. Polymorphisms in this gene may be associated with susceptibility to schizophrenia. [provided by RefSeq, Jul 2008]
Gene Name: Sulfotransferase Family 4A Member 1
Chromosome: CHR22: 44220386 -44258378
Locus: 22q13.31
Gene Diseases
The SULT4A1 TFIP11 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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