FAM168A-SYT12 Fusion FISH Probe
The FAM168A-SYT12 Fusion FISH Probe is used to confirm a fusion of the FAM168A and SYT12 genes. The fusion of the FAM168A and SYT12 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. 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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| FAM168A-SYT12-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-RERE | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-REOR | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-REGO | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-REGR | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-REAQ | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-ORRE | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-OROR | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-ORGO | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-ORAQ | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-GORE | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-GOOR | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-GOGO | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-GOGR | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-GOAQ | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-GRRE | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-GROR | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-GRGO | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-GRGR | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-GRAQ | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-AQRE | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-AQOR | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-AQGO | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-AQGR | 20 (40 μL) | 200 μL |
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| FAM168A-SYT12-20-AQAQ | 20 (40 μL) | 200 μL |
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FAM168A Gene Summary
The Family With Sequence Similarity 168 Member A (FAM168A) gene is located on chr11 :73117027-73309228 at 11q13.4.
Gene Name: Family With Sequence Similarity 168 Member A
Chromosome: CHR11: 73117027 -73309228
Locus: 11q13.4
SYT12 Gene Summary
This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that mediate calcium-dependent regulation of membrane trafficking in synaptic transmission. Studies of the orthologous gene in rat have shown that the encoded protein selectively modulates spontaneous synaptic-vesicle exocytosis and may also be involved in regulating calcium independent secretion in nonneuronal cells. Alternative splicing results in multiple transcript variants. The gene has previously been referred to as synaptotagmin XI but has been renamed synaptotagmin XII to be standard with mouse and rat official nomenclature.[provided by RefSeq, Apr 2010]
Gene Name: Synaptotagmin 12
Chromosome: CHR11: 66790189 -66818334
Locus: 11q13.2
Gene Diseases
The FAM168A SYT12 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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