TMCC2-NBEA Fusion FISH Probe
The TMCC2-NBEA Fusion FISH Probe is used to confirm a fusion of the TMCC2 and NBEA genes. The fusion of the TMCC2 and NBEA genes has been associated with Pheochromocytoma And Paraganglioma. 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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| TMCC2-NBEA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-RERE | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-REOR | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-REGO | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-REGR | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-REAQ | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-ORRE | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-OROR | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-ORGO | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-ORAQ | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-GORE | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-GOOR | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-GOGO | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-GOGR | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-GOAQ | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-GRRE | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-GROR | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-GRGO | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-GRGR | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-GRAQ | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-AQRE | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-AQOR | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-AQGO | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-AQGR | 20 (40 μL) | 200 μL |
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| TMCC2-NBEA-20-AQAQ | 20 (40 μL) | 200 μL |
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TMCC2 Gene Summary
The Transmembrane And Coiled-coil Domain Family 2 (TMCC2) gene is located on chr1 :205197037-205242471 at 1q32.1.
Gene Name: Transmembrane And Coiled-coil Domain Family 2
Chromosome: CHR1: 205197037 -205242471
Locus: 1q32.1
NBEA Gene Summary
This gene encodes a member of a large, diverse group of A-kinase anchor proteins that target the activity of protein kinase A to specific subcellular sites by binding to its type II regulatory subunits. Brain-specific expression and coat protein-like membrane recruitment of a highly similar protein in mouse suggest an involvement in neuronal post-Golgi membrane traffic. Mutations in this gene may be associated with a form of autism. This gene and its expression are frequently disrupted in patients with multiple myeloma. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants may exist, but their full-length nature has not been determined.[provided by RefSeq, Feb 2011]
Gene Name: Neurobeachin
Chromosome: CHR13: 35516423 -36246873
Locus: 13q13.3
Gene Diseases
The TMCC2 NBEA Fusion has been associated with the following diseases:
| Disease Name |
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| Pheochromocytoma And Paraganglioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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