NFATC2IP-KIAA0556 Fusion FISH Probe
The NFATC2IP-KIAA0556 Fusion FISH Probe is used to confirm a fusion of the NFATC2IP and KIAA0556 genes. The fusion of the NFATC2IP and KIAA0556 genes has been associated with Sarcoma. 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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| NFATC2IP-KIAA0556-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-RERE | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-REOR | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-REGO | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-REGR | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-REAQ | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-ORRE | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-OROR | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-ORGO | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-ORAQ | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-GORE | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-GOOR | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-GOGO | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-GOGR | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-GOAQ | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-GRRE | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-GROR | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-GRGO | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-GRGR | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-GRAQ | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-AQRE | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-AQOR | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-AQGO | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-AQGR | 20 (40 μL) | 200 μL |
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| NFATC2IP-KIAA0556-20-AQAQ | 20 (40 μL) | 200 μL |
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KIAA0556 Gene Summary
This gene encodes a novel, evolutionarily conserved, ciliary protein. In human hTERT-RPE1 cells, the protein is found at the base of cilia, decorating the ciliary axoneme, and enriched at the ciliary tip. The protein binds to microtubules in vitro and regulates their stability when it is overexpressed. A null mutation in this gene has been associated with Joubert syndrome, a recessive disorder that is characterized by a distinctive mid-hindbrain and cerebellar malformation and is also often associated with wider ciliopathy symptoms. Consistently, in a serum-starvation ciliogenesis assay, human fibroblast cells derived from patients with the mutation display a reduced number of ciliated cells with abnormally long cilia. [provided by RefSeq, Feb 2016]
Gene Name:
Chromosome: CHR16: 27561467 -27791692
Locus: 16p12.1
NFATC2IP Gene Summary
The Nuclear Factor Of Activated T-cells 2 Interacting Protein (NFATC2IP) gene is located on chr16 :28962317-28977767 at 16p11.2.
Gene Name: Nuclear Factor Of Activated T-cells 2 Interacting Protein
Chromosome: CHR16: 28962317 -28977767
Locus: 16p11.2
Gene Diseases
The NFATC2IP KIAA0556 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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