OSBPL8-PTPRQ Fusion FISH Probe
The OSBPL8-PTPRQ Fusion FISH Probe is used to confirm a fusion of the OSBPL8 and PTPRQ genes. The fusion of the OSBPL8 and PTPRQ genes has been associated with Sarcoma. 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
SKU | Test Kits | Buffer | Dye Color | Order Now |
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OSBPL8-PTPRQ-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-RERE | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-REOR | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-REGO | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-REGR | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-REAQ | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-ORRE | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-OROR | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-ORGO | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-ORAQ | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-GORE | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-GOOR | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-GOGO | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-GOGR | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-GOAQ | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-GRRE | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-GROR | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-GRGO | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-GRGR | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-GRAQ | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-AQRE | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-AQOR | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-AQGO | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-AQGR | 20 (40 μL) | 200 μL | ||
OSBPL8-PTPRQ-20-AQAQ | 20 (40 μL) | 200 μL |
OSBPL8 Gene Summary
This gene encodes a member of a family of proteins containing an N-terminal pleckstrin homology domain and a highly conserved C-terminal oxysterol-binding protein-like sterol-binding domain. It binds mutliple lipid-containing molecules, including phosphatidylserine, phosphatidylinositol 4-phosphate (PI4P) and oxysterol, and promotes their exchange between the endoplasmic reticulum and the plasma membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Gene Name: Oxysterol Binding Protein Like 8
Chromosome: CHR12: 76745577 -76953589
Locus: 12q21.2
PTPRQ Gene Summary
This locus encodes a member of the type III receptor-like protein-tyrosine phosphatase family. The encoded protein catalyzes the dephosphorylation of phosphotyrosine and phosphatidylinositol and plays roles in cellular proliferation and differentiation. Mutations at this locus have been linked to autosomal recessive deafness. [provided by RefSeq, Mar 2014]
Gene Name: Protein Tyrosine Phosphatase, Receptor Type Q
Chromosome: CHR12: 80838125 -81073968
Locus: 12q21.31
Gene Diseases
The OSBPL8 PTPRQ Fusion has been associated with the following diseases:
Disease Name |
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Sarcoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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