IL17D-IFT88 Fusion FISH Probe
The IL17D-IFT88 Fusion FISH Probe is used to confirm a fusion of the IL17D and IFT88 genes. The fusion of the IL17D and IFT88 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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| IL17D-IFT88-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-RERE | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-REOR | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-REGO | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-REGR | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-REAQ | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-ORRE | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-OROR | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-ORGO | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-ORAQ | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-GORE | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-GOOR | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-GOGO | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-GOGR | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-GOAQ | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-GRRE | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-GROR | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-GRGO | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-GRGR | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-GRAQ | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-AQRE | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-AQOR | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-AQGO | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-AQGR | 20 (40 μL) | 200 μL |
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| IL17D-IFT88-20-AQAQ | 20 (40 μL) | 200 μL |
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IFT88 Gene Summary
This gene encodes a member of the tetratrico peptide repeat (TPR) family. The encoded protein is involved in cilium biogenesis. Mutations of a similar gene in mouse can cause polycystic kidney disease. Several transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2017]
Gene Name: Intraflagellar Transport 88
Chromosome: CHR13: 21141207 -21265576
Locus: 13q12.11
IL17D Gene Summary
The protein encoded by this gene is a cytokine that shares the sequence similarity with IL17. The treatment of endothelial cells with this cytokine has been shown to stimulate the production of other cytokines including IL6, IL8 and CSF2/ GM-CSF. The increased expression of IL8 induced by this cytokine was found to be NF-kappa B-dependent. [provided by RefSeq, Jul 2008]
Gene Name: Interleukin 17D
Chromosome: CHR13: 21277481 -21297237
Locus: 13q12.11
Gene Diseases
The IL17D IFT88 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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