NBEAL2-TMC2 Fusion FISH Probe
The NBEAL2-TMC2 Fusion FISH Probe is used to confirm a fusion of the NBEAL2 and TMC2 genes. The fusion of the NBEAL2 and TMC2 genes has been associated with Breast Invasive 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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| NBEAL2-TMC2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-RERE | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-REOR | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-REGO | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-REGR | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-REAQ | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-ORRE | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-OROR | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-ORGO | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-ORAQ | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-GORE | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-GOOR | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-GOGO | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-GOGR | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-GOAQ | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-GRRE | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-GROR | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-GRGO | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-GRGR | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-GRAQ | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-AQRE | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-AQOR | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-AQGO | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-AQGR | 20 (40 μL) | 200 μL |
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| NBEAL2-TMC2-20-AQAQ | 20 (40 μL) | 200 μL |
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NBEAL2 Gene Summary
The protein encoded by this gene contains a beige and Chediak-Higashi (BEACH) domain and multiple WD40 domains, and may play a role in megakaryocyte alpha-granule biogenesis. Mutations in this gene are a cause of gray platelet syndrome. [provided by RefSeq, Dec 2011]
Gene Name: Neurobeachin Like 2
Chromosome: CHR3: 47021172 -47051193
Locus: 3p21.31
TMC2 Gene Summary
This gene encodes a transmembrane protein that is necesssary for mechanotransduction in cochlear hair cells of the inner ear. Mutations in this gene may underlie hereditary disorders of balance and hearing. [provided by RefSeq, Aug 2015]
Gene Name: Transmembrane Channel Like 2
Chromosome: CHR20: 2517252 -2622430
Locus: 20p13
Gene Diseases
The NBEAL2 TMC2 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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