NTN4-PAH Fusion FISH Probe
The NTN4-PAH Fusion FISH Probe is used to confirm a fusion of the NTN4 and PAH genes. The fusion of the NTN4 and PAH genes has been associated with Adrenocortical 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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| NTN4-PAH-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-RERE | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-REOR | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-REGO | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-REGR | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-REAQ | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-ORRE | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-OROR | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-ORGO | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-ORAQ | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-GORE | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-GOOR | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-GOGO | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-GOGR | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-GOAQ | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-GRRE | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-GROR | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-GRGO | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-GRGR | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-GRAQ | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-AQRE | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-AQOR | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-AQGO | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-AQGR | 20 (40 μL) | 200 μL |
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| NTN4-PAH-20-AQAQ | 20 (40 μL) | 200 μL |
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PAH Gene Summary
This gene encodes a member of the biopterin-dependent aromatic amino acid hydroxylase protein family. The encoded phenylalanine hydroxylase enzyme hydroxylates phenylalanine to tyrosine and is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria. [provided by RefSeq, Aug 2017]
Gene Name: Phenylalanine Hydroxylase
Chromosome: CHR12: 103232103 -103311381
Locus: 12q23.2
NTN4 Gene Summary
This gene encodes a member of the netrin family of proteins, which function in various biological processes including axon guidance, tumorogenesis, and angiogenesis. Netrins are laminin-related proteins that have an N-terminal laminin-type domain, epidermal growth factor-like repeat domain, and a positively charged heparin-binding domain at the C-terminus. The protein encoded by this gene is involved in processes including neurite growth and migration, angiogenesis and mural cell adhesion to endothelial cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]
Gene Name: Netrin 4
Chromosome: CHR12: 96051582 -96184536
Locus: 12q22
Gene Diseases
The NTN4 PAH Fusion has been associated with the following diseases:
| Disease Name |
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| Adrenocortical Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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