SCNN1G-COL27A1 Fusion FISH Probe
The SCNN1G-COL27A1 Fusion FISH Probe is used to confirm a fusion of the SCNN1G and COL27A1 genes. The fusion of the SCNN1G and COL27A1 genes has been associated with Breast Invasive 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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| SCNN1G-COL27A1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-RERE | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-REOR | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-REGO | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-REGR | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-REAQ | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-ORRE | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-OROR | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-ORGO | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-ORAQ | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-GORE | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-GOOR | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-GOGO | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-GOGR | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-GOAQ | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-GRRE | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-GROR | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-GRGO | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-GRGR | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-GRAQ | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-AQRE | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-AQOR | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-AQGO | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-AQGR | 20 (40 μL) | 200 μL |
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| SCNN1G-COL27A1-20-AQAQ | 20 (40 μL) | 200 μL |
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SCNN1G Gene Summary
Nonvoltage-gated, amiloride-sensitive, sodium channels control fluid and electrolyte transport across epithelia in many organs. These channels are heteromeric complexes consisting of 3 subunits: alpha, beta, and gamma. This gene encodes the gamma subunit, and mutations in this gene have been associated with Liddle syndrome. [provided by RefSeq, Apr 2009]
Gene Name: Sodium Channel Epithelial 1 Gamma Subunit
Chromosome: CHR16: 23194039 -23228200
Locus: 16p12.2
COL27A1 Gene Summary
This gene encodes a member of the fibrillar collagen family, and plays a role during the calcification of cartilage and the transition of cartilage to bone. The encoded protein product is a preproprotein. It includes an N-terminal signal peptide, which is followed by an N-terminal propetide, mature peptide and a C-terminal propeptide. The N-terminal propeptide contains thrombospondin N-terminal-like and laminin G-like domains. The mature peptide is a major triple-helical region. The C-terminal propeptide, also known as COLFI domain, plays crucial roles in tissue growth and repair. Mutations in this gene cause Steel syndrome. Alternatively spliced transcript variants have been found, but the full-length nature of some variants has not been determined. [provided by RefSeq, Sep 2014]
Gene Name: Collagen Type XXVII Alpha 1 Chain
Chromosome: CHR9: 116918230 -117072975
Locus: 9q32
Gene Diseases
The SCNN1G COL27A1 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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