NFAT5-FHOD1 Fusion FISH Probe
The NFAT5-FHOD1 Fusion FISH Probe is used to confirm a fusion of the NFAT5 and FHOD1 genes. The fusion of the NFAT5 and FHOD1 genes has been associated with Lung Adenocarcinoma. 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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| NFAT5-FHOD1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-RERE | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-REOR | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-REGO | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-REGR | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-REAQ | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-ORRE | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-OROR | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-ORGO | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-ORAQ | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-GORE | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-GOOR | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-GOGO | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-GOGR | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-GOAQ | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-GRRE | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-GROR | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-GRGO | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-GRGR | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-GRAQ | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-AQRE | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-AQOR | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-AQGO | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-AQGR | 20 (40 μL) | 200 μL |
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| NFAT5-FHOD1-20-AQAQ | 20 (40 μL) | 200 μL |
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NFAT5 Gene Summary
The product of this gene is a member of the nuclear factors of activated T cells family of transcription factors. Proteins belonging to this family play a central role in inducible gene transcription during the immune response. This protein regulates gene expression induced by osmotic stress in mammalian cells. Unlike monomeric members of this protein family, this protein exists as a homodimer and forms stable dimers with DNA elements. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Nuclear Factor Of Activated T-cells 5
Chromosome: CHR16: 69599868 -69738569
Locus: 16q22.1
FHOD1 Gene Summary
This gene encodes a protein which is a member of the formin/diaphanous family of proteins. The gene is ubiquitously expressed but is found in abundance in the spleen. The encoded protein has sequence homology to diaphanous and formin proteins within the Formin Homology (FH)1 and FH2 domains. It also contains a coiled-coil domain, a collagen-like domain, two nuclear localization signals, and several potential PKC and PKA phosphorylation sites. It is a predominantly cytoplasmic protein and is expressed in a variety of human cell lines. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]
Gene Name: Formin Homology 2 Domain Containing 1
Chromosome: CHR16: 67263291 -67281425
Locus: 16q22.1
Gene Diseases
The NFAT5 FHOD1 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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