EDA-FAAH2 Fusion FISH Probe
The EDA-FAAH2 Fusion FISH Probe is used to confirm a fusion of the EDA and FAAH2 genes. The fusion of the EDA and FAAH2 genes has been associated with Liver Hepatocellular 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. 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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| EDA-FAAH2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-RERE | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-REOR | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-REGO | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-REGR | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-REAQ | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-ORRE | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-OROR | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-ORGO | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-ORAQ | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-GORE | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-GOOR | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-GOGO | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-GOGR | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-GOAQ | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-GRRE | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-GROR | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-GRGO | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-GRGR | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-GRAQ | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-AQRE | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-AQOR | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-AQGO | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-AQGR | 20 (40 μL) | 200 μL |
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| EDA-FAAH2-20-AQAQ | 20 (40 μL) | 200 μL |
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EDA Gene Summary
The protein encoded by this gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia. Several transcript variants encoding many different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Ectodysplasin A
Chromosome: CHRX: 68835910 -69259321
Locus: Xq13.1
FAAH2 Gene Summary
This gene encodes a fatty acid amide hydrolase that shares a conserved protein motif with the amidase signature family of enzymes. The encoded enzyme is able to catalyze the hydrolysis of a broad range of bioactive lipids, including those from the three main classes of fatty acid amides; N-acylethanolamines, fatty acid primary amides and N-acyl amino acids. This enzyme has a preference for monounsaturated acyl chains as a substrate. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2017]
Gene Name: Fatty Acid Amide Hydrolase 2
Chromosome: CHRX: 57313109 -57515629
Locus: Xp11.21
Gene Diseases
The EDA FAAH2 Fusion has been associated with the following diseases:
| Disease Name |
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| Liver Hepatocellular Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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