SYN1-ATAD1 Fusion FISH Probe
The SYN1-ATAD1 Fusion FISH Probe is used to confirm a fusion of the SYN1 and ATAD1 genes. The fusion of the SYN1 and ATAD1 genes has been associated with Brain Lower Grade Glioma. 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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| SYN1-ATAD1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-RERE | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-REOR | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-REGO | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-REGR | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-REAQ | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-ORRE | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-OROR | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-ORGO | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-ORAQ | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-GORE | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-GOOR | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-GOGO | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-GOGR | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-GOAQ | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-GRRE | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-GROR | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-GRGO | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-GRGR | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-GRAQ | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-AQRE | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-AQOR | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-AQGO | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-AQGR | 20 (40 μL) | 200 μL |
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| SYN1-ATAD1-20-AQAQ | 20 (40 μL) | 200 μL |
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SYN1 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 plays a role in regulation of axonogenesis and synaptogenesis. The protein encoded serves as a substrate for several different protein kinases and phosphorylation may function in the regulation of this protein in the nerve terminal. Mutations in this gene may be associated with X-linked disorders with primary neuronal degeneration such as Rett syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Gene Name: Synapsin I
Chromosome: CHRX: 47431299 -47479256
Locus: Xp11.3-p11.23
ATAD1 Gene Summary
The ATPase Family, AAA Domain Containing 1 (ATAD1) gene is located on chr10 :89512874-89577917 at 10q23.31.
Gene Name: ATPase Family, AAA Domain Containing 1
Chromosome: CHR10: 89512874 -89577917
Locus: 10q23.31
Gene Diseases
The SYN1 ATAD1 Fusion has been associated with the following diseases:
| Disease Name |
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| Brain Lower Grade Glioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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