SAMD12-SNTB1 Fusion FISH Probe
The SAMD12-SNTB1 Fusion FISH Probe is used to confirm a fusion of the SAMD12 and SNTB1 genes. The fusion of the SAMD12 and SNTB1 genes has been associated with Ovarian Serous Cystadenocarcinoma. 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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| SAMD12-SNTB1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-RERE | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-REOR | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-REGO | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-REGR | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-REAQ | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-ORRE | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-OROR | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-ORGO | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-ORAQ | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-GORE | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-GOOR | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-GOGO | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-GOGR | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-GOAQ | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-GRRE | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-GROR | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-GRGO | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-GRGR | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-GRAQ | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-AQRE | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-AQOR | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-AQGO | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-AQGR | 20 (40 μL) | 200 μL |
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| SAMD12-SNTB1-20-AQAQ | 20 (40 μL) | 200 μL |
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SNTB1 Gene Summary
Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally-related genes. [provided by RefSeq, Jul 2008]
Gene Name: Syntrophin Beta 1
Chromosome: CHR8: 121547984 -121824309
Locus: 8q24.12
SAMD12 Gene Summary
The Sterile Alpha Motif Domain Containing 12 (SAMD12) gene is located on chr8 :119201694-119634184 at 8q24.11-q24.12.
Gene Name: Sterile Alpha Motif Domain Containing 12
Chromosome: CHR8: 119201694 -119634184
Locus: 8q24.11-q24.12
Gene Diseases
The SAMD12 SNTB1 Fusion has been associated with the following diseases:
| Disease Name |
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| Ovarian Serous Cystadenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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