RASSF3-SNX10 Fusion FISH Probe
The RASSF3-SNX10 Fusion FISH Probe is used to confirm a fusion of the RASSF3 and SNX10 genes. The fusion of the RASSF3 and SNX10 genes has been associated with Brain Lower Grade Glioma. 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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RASSF3-SNX10-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-RERE | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-REOR | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-REGO | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-REGR | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-REAQ | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-ORRE | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-OROR | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-ORGO | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-ORAQ | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-GORE | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-GOOR | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-GOGO | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-GOGR | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-GOAQ | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-GRRE | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-GROR | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-GRGO | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-GRGR | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-GRAQ | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-AQRE | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-AQOR | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-AQGO | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-AQGR | 20 (40 μL) | 200 μL | ||
RASSF3-SNX10-20-AQAQ | 20 (40 μL) | 200 μL |
SNX10 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 does not contain a coiled coil region, like some family members. This gene may play a role in regulating endosome homeostasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]
Gene Name: Sorting Nexin 10
Chromosome: CHR7: 26331514 -26413949
Locus: 7p15.2
RASSF3 Gene Summary
The RAS oncogene (MIM 190020) is mutated in nearly one-third of all human cancers. Members of the RAS superfamily are plasma membrane GTP-binding proteins that modulate intracellular signal transduction pathways. A subfamily of RAS effectors, including RASSF3, share a RAS association (RA) domain.[supplied by OMIM, Jul 2003]
Gene Name: Ras Association Domain Family Member 3
Chromosome: CHR12: 65004292 -65091347
Locus: 12q14.2
Gene Diseases
The RASSF3 SNX10 Fusion has been associated with the following diseases:
Disease Name |
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Brain Lower Grade Glioma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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