ERICH1-IYD Fusion FISH Probe
The ERICH1-IYD Fusion FISH Probe is used to confirm a fusion of the ERICH1 and IYD genes. The fusion of the ERICH1 and IYD genes has been associated with Lung Squamous Cell 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| ERICH1-IYD-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-RERE | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-REOR | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-REGO | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-REGR | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-REAQ | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-ORRE | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-OROR | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-ORGO | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-ORAQ | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-GORE | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-GOOR | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-GOGO | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-GOGR | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-GOAQ | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-GRRE | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-GROR | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-GRGO | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-GRGR | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-GRAQ | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-AQRE | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-AQOR | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-AQGO | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-AQGR | 20 (40 μL) | 200 μL |
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| ERICH1-IYD-20-AQAQ | 20 (40 μL) | 200 μL |
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ERICH1 Gene Summary
The Glutamate Rich 1 (ERICH1) gene is located on chr8 :614199-681226 at 8p23.3.
Gene Name: Glutamate Rich 1
Chromosome: CHR8: 614199 -681226
Locus: 8p23.3
IYD Gene Summary
This gene encodes an enzyme that catalyzes the oxidative NADPH-dependent deiodination of mono- and diiodotyrosine, which are the halogenated byproducts of thyroid hormone production. The N-terminus of the protein functions as a membrane anchor. Mutations in this gene cause congenital hypothyroidism due to dyshormonogenesis type 4, which is also referred to as deiodinase deficiency, or iodotyrosine dehalogenase deficiency, or thyroid hormonogenesis type 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
Gene Name: Iodotyrosine Deiodinase
Chromosome: CHR6: 150690027 -150725765
Locus: 6q25.1
Gene Diseases
The ERICH1 IYD Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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