FSTL1-CPOX Fusion FISH Probe
The FSTL1-CPOX Fusion FISH Probe is used to confirm a fusion of the FSTL1 and CPOX genes. The fusion of the FSTL1 and CPOX 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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| FSTL1-CPOX-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-RERE | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-REOR | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-REGO | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-REGR | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-REAQ | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-ORRE | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-OROR | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-ORGO | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-ORAQ | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-GORE | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-GOOR | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-GOGO | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-GOGR | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-GOAQ | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-GRRE | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-GROR | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-GRGO | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-GRGR | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-GRAQ | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-AQRE | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-AQOR | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-AQGO | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-AQGR | 20 (40 μL) | 200 μL |
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| FSTL1-CPOX-20-AQAQ | 20 (40 μL) | 200 μL |
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CPOX Gene Summary
The protein encoded by this gene is the sixth enzyme of the heme biosynthetic pathway. The encoded enzyme is soluble and found in the intermembrane space of mitochondria. This enzyme catalyzes the stepwise oxidative decarboxylation of coproporphyrinogen III to protoporphyrinogen IX, a precursor of heme. Defects in this gene are a cause of hereditary coproporphyria (HCP).[provided by RefSeq, Oct 2009]
Gene Name: Coproporphyrinogen Oxidase
Chromosome: CHR3: 98298289 -98312455
Locus: 3q11.2
FSTL1 Gene Summary
This gene encodes a protein with similarity to follistatin, an activin-binding protein. It contains an FS module, a follistatin-like sequence containing 10 conserved cysteine residues. This gene product is thought to be an autoantigen associated with rheumatoid arthritis. [provided by RefSeq, Jul 2008]
Gene Name: Follistatin Like 1
Chromosome: CHR3: 120113060 -120169918
Locus: 3q13.33
Gene Diseases
The FSTL1 CPOX 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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