SCMH1-CUL3 Fusion FISH Probe
The SCMH1-CUL3 Fusion FISH Probe is used to confirm a fusion of the SCMH1 and CUL3 genes. The fusion of the SCMH1 and CUL3 genes has been associated with Lung Adenocarcinoma. 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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| SCMH1-CUL3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-RERE | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-REOR | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-REGO | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-REGR | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-REAQ | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-ORRE | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-OROR | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-ORGO | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-ORAQ | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-GORE | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-GOOR | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-GOGO | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-GOGR | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-GOAQ | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-GRRE | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-GROR | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-GRGO | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-GRGR | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-GRAQ | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-AQRE | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-AQOR | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-AQGO | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-AQGR | 20 (40 μL) | 200 μL |
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| SCMH1-CUL3-20-AQAQ | 20 (40 μL) | 200 μL |
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CUL3 Gene Summary
This gene encodes a member of the cullin protein family. The encoded protein plays a critical role in the polyubiquitination and subsequent degradation of specific protein substrates as the core component and scaffold protein of an E3 ubiquitin ligase complex. Complexes including the encoded protein may also play a role in late endosome maturation. Mutations in this gene are a cause of type 2E pseudohypoaldosteronism. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]
Gene Name: Cullin 3
Chromosome: CHR2: 225334868 -225450110
Locus: 2q36.2
SCMH1 Gene Summary
The Scm Polycomb Group Protein Homolog 1 (SCMH1) gene is located on chr1 :41492870-41707815 at 1p34.2.
Gene Name: Scm Polycomb Group Protein Homolog 1
Chromosome: CHR1: 41492870 -41707815
Locus: 1p34.2
Gene Diseases
The SCMH1 CUL3 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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