NRSN2-OSBPL1A Fusion FISH Probe
The NRSN2-OSBPL1A Fusion FISH Probe is used to confirm a fusion of the NRSN2 and OSBPL1A genes. The fusion of the NRSN2 and OSBPL1A genes has been associated with Skin Cutaneous Melanoma. 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 |
---|---|---|---|---|
NRSN2-OSBPL1A-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-RERE | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-REOR | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-REGO | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-REGR | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-REAQ | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-ORRE | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-OROR | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-ORGO | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-ORAQ | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-GORE | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-GOOR | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-GOGO | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-GOGR | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-GOAQ | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-GRRE | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-GROR | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-GRGO | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-GRGR | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-GRAQ | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-AQRE | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-AQOR | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-AQGO | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-AQGR | 20 (40 μL) | 200 μL | ||
NRSN2-OSBPL1A-20-AQAQ | 20 (40 μL) | 200 μL |
NRSN2 Gene Summary
The Neurensin 2 (NRSN2) gene is located on chr20 :327369-335512 at 20p13.
Gene Name: Neurensin 2
Chromosome: CHR20: 327369 -335512
Locus: 20p13
OSBPL1A Gene Summary
This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Most members contain an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain, although some members contain only the sterol-binding domain. Transcript variants derived from alternative promoter usage and/or alternative splicing exist; they encode different isoforms. [provided by RefSeq, Jul 2008]
Gene Name: Oxysterol Binding Protein Like 1A
Chromosome: CHR18: 21742010 -21977833
Locus: 18q11.2
Gene Diseases
The NRSN2 OSBPL1A Fusion has been associated with the following diseases:
Disease Name |
---|
Skin Cutaneous Melanoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
---|