SCMH1-SHISA5 Fusion FISH Probe
The SCMH1-SHISA5 Fusion FISH Probe is used to confirm a fusion of the SCMH1 and SHISA5 genes. The fusion of the SCMH1 and SHISA5 genes has been associated with Head And Neck Squamous Cell Carcinoma . 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-SHISA5-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-RERE | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-REOR | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-REGO | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-REGR | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-REAQ | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-ORRE | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-OROR | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-ORGO | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-ORAQ | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-GORE | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-GOOR | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-GOGO | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-GOGR | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-GOAQ | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-GRRE | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-GROR | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-GRGO | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-GRGR | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-GRAQ | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-AQRE | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-AQOR | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-AQGO | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-AQGR | 20 (40 μL) | 200 μL |
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| SCMH1-SHISA5-20-AQAQ | 20 (40 μL) | 200 μL |
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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
SHISA5 Gene Summary
This gene encodes a member of the shisa family. The encoded protein is localized to the endoplasmic reticulum, and together with p53 induces apoptosis in a caspase-dependent manner. Alternative splicing results in multiple transcript variants. Related pseudogenes of this gene are found on chromosome X. [provided by RefSeq, Apr 2016]
Gene Name: Shisa Family Member 5
Chromosome: CHR3: 48509196 -48541661
Locus: 3p21.31
Gene Diseases
The SCMH1 SHISA5 Fusion has been associated with the following diseases:
| Disease Name |
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| Head And Neck Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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