HMGCS1-OXCT1 Fusion FISH Probe
The HMGCS1-OXCT1 Fusion FISH Probe is used to confirm a fusion of the HMGCS1 and OXCT1 genes. The fusion of the HMGCS1 and OXCT1 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. 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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| HMGCS1-OXCT1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-RERE | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-REOR | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-REGO | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-REGR | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-REAQ | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-ORRE | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-OROR | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-ORGO | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-ORAQ | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-GORE | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-GOOR | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-GOGO | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-GOGR | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-GOAQ | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-GRRE | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-GROR | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-GRGO | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-GRGR | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-GRAQ | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-AQRE | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-AQOR | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-AQGO | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-AQGR | 20 (40 μL) | 200 μL |
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| HMGCS1-OXCT1-20-AQAQ | 20 (40 μL) | 200 μL |
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HMGCS1 Gene Summary
The 3-hydroxy-3-methylglutaryl-CoA Synthase 1 (HMGCS1) gene is located on chr5 :43289492-43313595 at 5p12.
Gene Name: 3-hydroxy-3-methylglutaryl-CoA Synthase 1
Chromosome: CHR5: 43289492 -43313595
Locus: 5p12
OXCT1 Gene Summary
This gene encodes a member of the 3-oxoacid CoA-transferase gene family. The encoded protein is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the reversible transfer of coenzyme A from succinyl-CoA to acetoacetate. Mutations in this gene are associated with succinyl CoA:3-oxoacid CoA transferase deficiency. [provided by RefSeq, Jul 2008]
Gene Name: 3-oxoacid CoA-transferase 1
Chromosome: CHR5: 41730166 -41870791
Locus: 5p13.1
Gene Diseases
The HMGCS1 OXCT1 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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