AKAP13-SYNE1 Fusion FISH Probe
The AKAP13-SYNE1 Fusion FISH Probe is used to confirm a fusion of the AKAP13 and SYNE1 genes. The fusion of the AKAP13 and SYNE1 genes has been associated with Kidney Renal Papillary Cell 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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| AKAP13-SYNE1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-RERE | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-REOR | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-REGO | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-REGR | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-REAQ | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-ORRE | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-OROR | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-ORGO | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-ORAQ | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-GORE | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-GOOR | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-GOGO | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-GOGR | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-GOAQ | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-GRRE | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-GROR | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-GRGO | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-GRGR | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-GRAQ | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-AQRE | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-AQOR | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-AQGO | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-AQGR | 20 (40 μL) | 200 μL |
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| AKAP13-SYNE1-20-AQAQ | 20 (40 μL) | 200 μL |
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AKAP13 Gene Summary
The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms containing c-terminal dbl oncogene homology (DH) and pleckstrin homology (PH) domains. The DH domain is associated with guanine nucleotide exchange activation for the Rho/Rac family of small GTP binding proteins, resulting in the conversion of the inactive GTPase to the active form capable of transducing signals. The PH domain has multiple functions. Therefore, these isoforms function as scaffolding proteins to coordinate a Rho signaling pathway, function as protein kinase A-anchoring proteins and, in addition, enhance ligand-dependent activity of estrogen receptors alpha and beta. [provided by RefSeq, Jul 2012]
Gene Name: A-kinase Anchoring Protein 13
Chromosome: CHR15: 85923870 -86292586
Locus: 15q25.3
SYNE1 Gene Summary
This gene encodes a spectrin repeat containing protein expressed in skeletal and smooth muscle, and peripheral blood lymphocytes, that localizes to the nuclear membrane. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia 8, also referred to as autosomal recessive cerebellar ataxia type 1 or recessive ataxia of Beauce. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Gene Name: Spectrin Repeat Containing Nuclear Envelope Protein 1
Chromosome: CHR6: 152442818 -152958534
Locus: 6q25.2
Gene Diseases
The AKAP13 SYNE1 Fusion has been associated with the following diseases:
| Disease Name |
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| Kidney Renal Papillary Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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