AIF1L-SYN2 Fusion FISH Probe
The AIF1L-SYN2 Fusion FISH Probe is used to confirm a fusion of the AIF1L and SYN2 genes. The fusion of the AIF1L and SYN2 genes has been associated with Skin Cutaneous Melanoma. 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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| AIF1L-SYN2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-RERE | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-REOR | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-REGO | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-REGR | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-REAQ | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-ORRE | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-OROR | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-ORGO | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-ORAQ | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-GORE | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-GOOR | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-GOGO | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-GOGR | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-GOAQ | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-GRRE | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-GROR | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-GRGO | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-GRGR | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-GRAQ | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-AQRE | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-AQOR | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-AQGO | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-AQGR | 20 (40 μL) | 200 μL |
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| AIF1L-SYN2-20-AQAQ | 20 (40 μL) | 200 μL |
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SYN2 Gene Summary
This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family encodes a neuron-specific phosphoprotein that selectively binds to small synaptic vesicles in the presynaptic nerve terminal. Polymorphisms in this gene are associated with abnormal presynaptic function and related neuronal disorders, including autism, epilepsy, bipolar disorder and schizophrenia. Alternative splicing of this gene results in multiple transcript variants. The tissue inhibitor of metalloproteinase 4 gene is located within an intron of this gene and is transcribed in the opposite direction. [provided by RefSeq, Feb 2014]
Gene Name: Synapsin II
Chromosome: CHR3: 12045861 -12233532
Locus: 3p25.2
AIF1L Gene Summary
The Allograft Inflammatory Factor 1 Like (AIF1L) gene is located on chr9 :133971862-133998539 at 9q34.12-q34.13.
Gene Name: Allograft Inflammatory Factor 1 Like
Chromosome: CHR9: 133971862 -133998539
Locus: 9q34.12-q34.13
Gene Diseases
The AIF1L SYN2 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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