NCKAP5-DYNC2H1 Fusion FISH Probe
The NCKAP5-DYNC2H1 Fusion FISH Probe is used to confirm a fusion of the NCKAP5 and DYNC2H1 genes. The fusion of the NCKAP5 and DYNC2H1 genes has been associated with Brain Lower Grade Glioma, and Brain Lower Grade Glioma. 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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| NCKAP5-DYNC2H1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-RERE | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-REOR | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-REGO | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-REGR | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-REAQ | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-ORRE | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-OROR | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-ORGO | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-ORAQ | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-GORE | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-GOOR | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-GOGO | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-GOGR | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-GOAQ | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-GRRE | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-GROR | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-GRGO | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-GRGR | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-GRAQ | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-AQRE | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-AQOR | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-AQGO | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-AQGR | 20 (40 μL) | 200 μL |
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| NCKAP5-DYNC2H1-20-AQAQ | 20 (40 μL) | 200 μL |
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DYNC2H1 Gene Summary
This gene encodes a large cytoplasmic dynein protein that is involved in retrograde transport in the cilium and has a role in intraflagellar transport, a process required for ciliary/flagellar assembly. Mutations in this gene cause a heterogeneous spectrum of conditions related to altered primary cilium function and often involve polydactyly, abnormal skeletogenesis, and polycystic kidneys. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jan 2010]
Gene Name: Dynein Cytoplasmic 2 Heavy Chain 1
Chromosome: CHR11: 102980159 -103350591
Locus: 11q22.3
NCKAP5 Gene Summary
The NCK Associated Protein 5 (NCKAP5) gene is located on chr2 :133429371-134326031 at 2q21.2.
Gene Name: NCK Associated Protein 5
Chromosome: CHR2: 133429371 -134326031
Locus: 2q21.2
Gene Diseases
The NCKAP5 DYNC2H1 Fusion has been associated with the following diseases:
| Disease Name |
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| Brain Lower Grade Glioma |
| Brain Lower Grade Glioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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