NECAP1-ANK1 Fusion FISH Probe
The NECAP1-ANK1 Fusion FISH Probe is used to confirm a fusion of the NECAP1 and ANK1 genes. The fusion of the NECAP1 and ANK1 genes has been associated with Bladder Urothelial 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| NECAP1-ANK1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-RERE | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-REOR | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-REGO | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-REGR | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-REAQ | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-ORRE | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-OROR | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-ORGO | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-ORAQ | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-GORE | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-GOOR | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-GOGO | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-GOGR | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-GOAQ | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-GRRE | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-GROR | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-GRGO | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-GRGR | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-GRAQ | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-AQRE | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-AQOR | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-AQGO | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-AQGR | 20 (40 μL) | 200 μL |
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| NECAP1-ANK1-20-AQAQ | 20 (40 μL) | 200 μL |
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ANK1 Gene Summary
Ankyrins are a family of proteins that link the integral membrane proteins to the underlying spectrin-actin cytoskeleton and play key roles in activities such as cell motility, activation, proliferation, contact and the maintenance of specialized membrane domains. Multiple isoforms of ankyrin with different affinities for various target proteins are expressed in a tissue-specific, developmentally regulated manner. Most ankyrins are typically composed of three structural domains: an amino-terminal domain containing multiple ankyrin repeats; a central region with a highly conserved spectrin binding domain; and a carboxy-terminal regulatory domain which is the least conserved and subject to variation. Ankyrin 1, the prototype of this family, was first discovered in the erythrocytes, but since has also been found in brain and muscles. Mutations in erythrocytic ankyrin 1 have been associated in approximately half of all patients with hereditary spherocytosis. Complex patterns of alternative splicing in the regulatory domain, giving rise to different isoforms of ankyrin 1 have been described. Truncated muscle-specific isoforms of ankyrin 1 resulting from usage of an alternate promoter have also been identified. [provided by RefSeq, Dec 2008]
Gene Name: Ankyrin 1
Chromosome: CHR8: 41510743 -41754280
Locus: 8p11.21
NECAP1 Gene Summary
This gene encodes a protein containing two characteristic WXXF motifs. The encoded protein localizes to clathrin-coated vesicles, where it binds components of the adapter protein complexes and aids in endocytosis. Loss of function of this gene results in early infantile epileptic encephalopathy-21. There is a pseudogene for this gene on chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]
Gene Name: NECAP Endocytosis Associated 1
Chromosome: CHR12: 8234806 -8250373
Locus: 12p13.31
Gene Diseases
The NECAP1 ANK1 Fusion has been associated with the following diseases:
| Disease Name |
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| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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