FNDC3B-TNIK Fusion FISH Probe
The FNDC3B-TNIK Fusion FISH Probe is used to confirm a fusion of the FNDC3B and TNIK genes. The fusion of the FNDC3B and TNIK genes has been associated with Esophageal 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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| FNDC3B-TNIK-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-RERE | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-REOR | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-REGO | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-REGR | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-REAQ | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-ORRE | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-OROR | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-ORGO | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-ORAQ | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-GORE | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-GOOR | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-GOGO | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-GOGR | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-GOAQ | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-GRRE | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-GROR | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-GRGO | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-GRGR | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-GRAQ | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-AQRE | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-AQOR | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-AQGO | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-AQGR | 20 (40 μL) | 200 μL |
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| FNDC3B-TNIK-20-AQAQ | 20 (40 μL) | 200 μL |
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TNIK Gene Summary
Wnt signaling plays important roles in carcinogenesis and embryonic development. The protein encoded by this gene is a serine/threonine kinase that functions as an activator of the Wnt signaling pathway. Mutations in this gene are associated with an autosomal recessive form of cognitive disability. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2017]
Gene Name: TRAF2 And NCK Interacting Kinase
Chromosome: CHR3: 170780291 -171178197
Locus: 3q26.2-q26.31
FNDC3B Gene Summary
The Fibronectin Type III Domain Containing 3B (FNDC3B) gene is located on chr3 :171757417-172118492 at 3q26.31.
Gene Name: Fibronectin Type III Domain Containing 3B
Chromosome: CHR3: 171757417 -172118492
Locus: 3q26.31
Gene Diseases
The FNDC3B TNIK Fusion has been associated with the following diseases:
| Disease Name |
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| Esophageal Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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