PCMTD2-SNX6 Fusion FISH Probe
The PCMTD2-SNX6 Fusion FISH Probe is used to confirm a fusion of the PCMTD2 and SNX6 genes. The fusion of the PCMTD2 and SNX6 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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PCMTD2-SNX6-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-RERE | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-REOR | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-REGO | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-REGR | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-REAQ | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-ORRE | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-OROR | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-ORGO | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-ORAQ | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-GORE | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-GOOR | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-GOGO | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-GOGR | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-GOAQ | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-GRRE | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-GROR | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-GRGO | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-GRGR | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-GRAQ | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-AQRE | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-AQOR | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-AQGO | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-AQGR | 20 (40 μL) | 200 μL | ||
PCMTD2-SNX6-20-AQAQ | 20 (40 μL) | 200 μL |
PCMTD2 Gene Summary
The Protein-L-isoaspartate (D-aspartate) O-methyltransferase Domain Containing 2 (PCMTD2) gene is located on chr20 :62887047-62907579 at 20q13.33.
Gene Name: Protein-L-isoaspartate (D-aspartate) O-methyltransferase Domain Containing 2
Chromosome: CHR20: 62887047 -62907579
Locus: 20q13.33
SNX6 Gene Summary
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein associates with the long isoform of the leptin receptor, the transforming growth factor-beta family of receptor serine-threonine kinases, and with receptor tyrosine kinases for platelet-derived growth factor, insulin, and epidermal growth factor. This protein may form oligomeric complexes with family member proteins through interactions of both the PX domain and the coiled coil regions of the molecules. Translocation of this protein from the cytoplasm to the nucleus occurs after binding to proviral integration site 1 protein. This gene results in two transcripts encoding two distinct isoforms. [provided by RefSeq, Jul 2008]
Gene Name: Sorting Nexin 6
Chromosome: CHR14: 35030617 -35099366
Locus: 14q13.1
Gene Diseases
The PCMTD2 SNX6 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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