OS9-C12ORF66 Fusion FISH Probe
The OS9-C12ORF66 Fusion FISH Probe is used to confirm a fusion of the OS9 and C12ORF66 genes. The fusion of the OS9 and C12ORF66 genes has been associated with Glioblastoma Multiforme. 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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OS9-C12ORF66-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-RERE | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-REOR | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-REGO | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-REGR | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-REAQ | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-ORRE | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-OROR | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-ORGO | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-ORAQ | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-GORE | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-GOOR | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-GOGO | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-GOGR | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-GOAQ | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-GRRE | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-GROR | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-GRGO | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-GRGR | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-GRAQ | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-AQRE | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-AQOR | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-AQGO | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-AQGR | 20 (40 μL) | 200 μL | ||
OS9-C12ORF66-20-AQAQ | 20 (40 μL) | 200 μL |
OS9 Gene Summary
This gene encodes a protein that is highly expressed in osteosarcomas. This protein binds to the hypoxia-inducible factor 1 (HIF-1), a key regulator of the hypoxic response and angiogenesis, and promotes the degradation of one of its subunits. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
Gene Name: OS9, Endoplasmic Reticulum Lectin
Chromosome: CHR12: 58087737 -58115340
Locus: 12q13.3-q14.1
C12orf66 Gene Summary
The Chromosome 12 Open Reading Frame 66 (C12orf66) gene is located on chr12 :64586418-64616076 at 12q14.2.
Gene Name: Chromosome 12 Open Reading Frame 66
Chromosome: CHR12: 64586418 -64616076
Locus: 12q14.2
Gene Diseases
The OS9 C12ORF66 Fusion has been associated with the following diseases:
Disease Name |
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Glioblastoma Multiforme |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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