UHRF1BP1L-CACNG3 Fusion FISH Probe
The UHRF1BP1L-CACNG3 Fusion FISH Probe is used to confirm a fusion of the UHRF1BP1L and CACNG3 genes. The fusion of the UHRF1BP1L and CACNG3 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| UHRF1BP1L-CACNG3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-RERE | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-REOR | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-REGO | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-REGR | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-REAQ | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-ORRE | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-OROR | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-ORGO | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-ORAQ | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-GORE | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-GOOR | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-GOGO | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-GOGR | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-GOAQ | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-GRRE | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-GROR | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-GRGO | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-GRGR | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-GRAQ | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-AQRE | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-AQOR | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-AQGO | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-AQGR | 20 (40 μL) | 200 μL |
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| UHRF1BP1L-CACNG3-20-AQAQ | 20 (40 μL) | 200 μL |
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CACNG3 Gene Summary
The protein encoded by this gene is a type I transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family. This gene is a susceptibility locus for childhood absence epilepsy. [provided by RefSeq, Dec 2010]
Gene Name: Calcium Voltage-gated Channel Auxiliary Subunit Gamma 3
Chromosome: CHR16: 24266873 -24373737
Locus: 16p12.1
UHRF1BP1L Gene Summary
The UHRF1 Binding Protein 1 Like (UHRF1BP1L) gene is located on chr12 :100430862-100536642 at 12q23.1.
Gene Name: UHRF1 Binding Protein 1 Like
Chromosome: CHR12: 100430862 -100536642
Locus: 12q23.1
Gene Diseases
The UHRF1BP1L CACNG3 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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