IDS-PHACTR1 Fusion FISH Probe
The IDS-PHACTR1 Fusion FISH Probe is used to confirm a fusion of the IDS and PHACTR1 genes. The fusion of the IDS and PHACTR1 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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| IDS-PHACTR1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-RERE | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-REOR | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-REGO | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-REGR | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-REAQ | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-ORRE | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-OROR | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-ORGO | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-ORAQ | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-GORE | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-GOOR | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-GOGO | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-GOGR | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-GOAQ | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-GRRE | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-GROR | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-GRGO | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-GRGR | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-GRAQ | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-AQRE | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-AQOR | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-AQGO | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-AQGR | 20 (40 μL) | 200 μL |
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| IDS-PHACTR1-20-AQAQ | 20 (40 μL) | 200 μL |
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IDS Gene Summary
This gene encodes a member of the sulfatase family of proteins. The encoded preproprotein is proteolytically processed to generate two polypeptide chains. This enzyme is involved in the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this gene are associated with the X-linked lysosomal storage disease mucopolysaccharidosis type II, also known as Hunter syndrome. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]
Gene Name: Iduronate 2-sulfatase
Chromosome: CHRX: 148560294 -148586884
Locus: Xq28
PHACTR1 Gene Summary
The protein encoded by this gene is a member of the phosphatase and actin regulator family of proteins. This family member can bind actin and regulate the reorganization of the actin cytoskeleton. It plays a role in tubule formation and in endothelial cell survival. Polymorphisms in this gene are associated with susceptibility to myocardial infarction, coronary artery disease and cervical artery dissection. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2016]
Gene Name: Phosphatase And Actin Regulator 1
Chromosome: CHR6: 12717036 -13288075
Locus: 6p24.1
Gene Diseases
The IDS PHACTR1 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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