CC2D1A-ZMYND8 Fusion FISH Probe
The CC2D1A-ZMYND8 Fusion FISH Probe is used to confirm a fusion of the CC2D1A and ZMYND8 genes. The fusion of the CC2D1A and ZMYND8 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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| CC2D1A-ZMYND8-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-RERE | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-REOR | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-REGO | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-REGR | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-REAQ | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-ORRE | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-OROR | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-ORGO | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-ORAQ | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-GORE | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-GOOR | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-GOGO | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-GOGR | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-GOAQ | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-GRRE | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-GROR | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-GRGO | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-GRGR | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-GRAQ | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-AQRE | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-AQOR | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-AQGO | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-AQGR | 20 (40 μL) | 200 μL |
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| CC2D1A-ZMYND8-20-AQAQ | 20 (40 μL) | 200 μL |
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ZMYND8 Gene Summary
The protein encoded by this gene is a receptor for activated C-kinase (RACK) protein. The encoded protein has been shown to bind in vitro to activated protein kinase C beta I. In addition, this protein is a cutaneous T-cell lymphoma-associated antigen. Finally, the protein contains a bromodomain and two zinc fingers, and is thought to be a transcriptional regulator. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Zinc Finger MYND-type Containing 8
Chromosome: CHR20: 45838380 -45985474
Locus: 20q13.12
CC2D1A Gene Summary
This gene encodes a transcriptional repressor that binds to a conserved 14-bp 5'-repressor element and regulates expression of the 5-hydroxytryptamine (serotonin) receptor 1A gene in neuronal cells. The DNA binding and transcriptional repressor activities of the protein are inhibited by calcium. A mutation in this gene results in a nonsyndromic form of cognitive disability (MRT3). [provided by RefSeq, Jul 2017]
Gene Name: Coiled-coil And C2 Domain Containing 1A
Chromosome: CHR19: 14016955 -14041693
Locus: 19p13.12
Gene Diseases
The CC2D1A ZMYND8 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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