WHSC1-CPLX1 Fusion FISH Probe
The WHSC1-CPLX1 Fusion FISH Probe is used to confirm a fusion of the WHSC1 and CPLX1 genes. The fusion of the WHSC1 and CPLX1 genes has been associated with Brain Lower Grade Glioma, and 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. 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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| WHSC1-CPLX1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-RERE | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-REOR | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-REGO | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-REGR | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-REAQ | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-ORRE | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-OROR | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-ORGO | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-ORAQ | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-GORE | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-GOOR | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-GOGO | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-GOGR | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-GOAQ | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-GRRE | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-GROR | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-GRGO | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-GRGR | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-GRAQ | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-AQRE | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-AQOR | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-AQGO | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-AQGR | 20 (40 μL) | 200 μL |
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| WHSC1-CPLX1-20-AQAQ | 20 (40 μL) | 200 μL |
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CPLX1 Gene Summary
Proteins encoded by the complexin/synaphin gene family are cytosolic proteins that function in synaptic vesicle exocytosis. These proteins bind syntaxin, part of the SNAP receptor. The protein product of this gene binds to the SNAP receptor complex and disrupts it, allowing transmitter release. [provided by RefSeq, Jul 2008]
Gene Name: Complexin 1
Chromosome: CHR4: 778744 -819945
Locus: 4p16.3
Gene Diseases
The WHSC1 CPLX1 Fusion has been associated with the following diseases:
| Disease Name |
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| Brain Lower Grade Glioma |
| Brain Lower Grade Glioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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