TSC1-SARDH Fusion FISH Probe
The TSC1-SARDH Fusion FISH Probe is used to confirm a fusion of the TSC1 and SARDH genes. The fusion of the TSC1 and SARDH genes has been associated with Liver Hepatocellular 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. 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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| TSC1-SARDH-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-RERE | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-REOR | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-REGO | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-REGR | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-REAQ | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-ORRE | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-OROR | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-ORGO | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-ORAQ | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-GORE | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-GOOR | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-GOGO | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-GOGR | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-GOAQ | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-GRRE | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-GROR | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-GRGO | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-GRGR | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-GRAQ | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-AQRE | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-AQOR | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-AQGO | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-AQGR | 20 (40 μL) | 200 μL |
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| TSC1-SARDH-20-AQAQ | 20 (40 μL) | 200 μL |
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SARDH Gene Summary
This gene encodes an enzyme localized to the mitochondrial matrix which catalyzes the oxidative demethylation of sarcosine. This enzyme is distinct from another mitochondrial matrix enzyme, dimethylglycine dehydrogenase, which catalyzes a reaction resulting in the formation of sarcosine. Mutations in this gene are associated with sarcosinemia. Alternatively spliced transcript variants have been described. [provided by RefSeq, Oct 2008]
Gene Name: Sarcosine Dehydrogenase
Chromosome: CHR9: 136528683 -136605077
Locus: 9q34.2
TSC1 Gene Summary
This gene encodes a growth inhibitory protein thought to play a role in the stabilization of tuberin. Mutations in this gene have been associated with tuberous sclerosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2009]
Gene Name: TSC Complex Subunit 1
Chromosome: CHR9: 135766734 -135820020
Locus: 9q34.13
Gene Diseases
The TSC1 SARDH Fusion has been associated with the following diseases:
| Disease Name |
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| Liver Hepatocellular Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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