IFT122-C3ORF37 Fusion FISH Probe
The IFT122-C3ORF37 Fusion FISH Probe is used to confirm a fusion of the IFT122 and C3ORF37 genes. The fusion of the IFT122 and C3ORF37 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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| IFT122-C3ORF37-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-RERE | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-REOR | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-REGO | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-REGR | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-REAQ | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-ORRE | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-OROR | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-ORGO | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-ORAQ | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-GORE | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-GOOR | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-GOGO | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-GOGR | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-GOAQ | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-GRRE | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-GROR | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-GRGO | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-GRGR | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-GRAQ | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-AQRE | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-AQOR | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-AQGO | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-AQGR | 20 (40 μL) | 200 μL |
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| IFT122-C3ORF37-20-AQAQ | 20 (40 μL) | 200 μL |
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IFT122 Gene Summary
This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This cytoplasmic protein contains seven WD repeats and an AF-2 domain which function by recruiting coregulatory molecules and in transcriptional activation. Mutations in this gene cause cranioectodermal dysplasia-1. A related pseudogene is located on chromosome 3. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
Gene Name: Intraflagellar Transport 122
Chromosome: CHR3: 129158967 -129239191
Locus: 3q21.3-q22.1
Gene Diseases
The IFT122 C3ORF37 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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