ZNF83-PCDH15 Fusion FISH Probe
The ZNF83-PCDH15 Fusion FISH Probe is used to confirm a fusion of the ZNF83 and PCDH15 genes. The fusion of the ZNF83 and PCDH15 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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ZNF83-PCDH15-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-RERE | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-REOR | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-REGO | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-REGR | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-REAQ | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-ORRE | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-OROR | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-ORGO | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-ORAQ | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-GORE | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-GOOR | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-GOGO | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-GOGR | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-GOAQ | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-GRRE | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-GROR | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-GRGO | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-GRGR | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-GRAQ | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-AQRE | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-AQOR | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-AQGO | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-AQGR | 20 (40 μL) | 200 μL | ||
ZNF83-PCDH15-20-AQAQ | 20 (40 μL) | 200 μL |
ZNF83 Gene Summary
The Zinc Finger Protein 83 (ZNF83) gene is located on chr19 :53115617-53193886 at 19q13.41.
Gene Name: Zinc Finger Protein 83
Chromosome: CHR19: 53115617 -53193886
Locus: 19q13.41
PCDH15 Gene Summary
This gene is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene result in hearing loss and Usher Syndrome Type IF (USH1F). Extensive alternative splicing resulting in multiple isoforms has been observed in the mouse ortholog. Similar alternatively spliced transcripts are inferred to occur in human, and additional variants are likely to occur. [provided by RefSeq, Dec 2008]
Gene Name: Protocadherin Related 15
Chromosome: CHR10: 55562532 -56561051
Locus: 10q21.1
Gene Diseases
The ZNF83 PCDH15 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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