IFNGR1-SMCHD1 Fusion FISH Probe
The IFNGR1-SMCHD1 Fusion FISH Probe is used to confirm a fusion of the IFNGR1 and SMCHD1 genes. The fusion of the IFNGR1 and SMCHD1 genes has been associated with Prostate Adenocarcinoma. 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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| IFNGR1-SMCHD1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-RERE | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-REOR | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-REGO | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-REGR | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-REAQ | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-ORRE | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-OROR | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-ORGO | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-ORAQ | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-GORE | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-GOOR | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-GOGO | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-GOGR | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-GOAQ | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-GRRE | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-GROR | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-GRGO | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-GRGR | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-GRAQ | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-AQRE | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-AQOR | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-AQGO | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-AQGR | 20 (40 μL) | 200 μL |
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| IFNGR1-SMCHD1-20-AQAQ | 20 (40 μL) | 200 μL |
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IFNGR1 Gene Summary
This gene (IFNGR1) encodes the ligand-binding chain (alpha) of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. A genetic variation in IFNGR1 is associated with susceptibility to Helicobacter pylori infection. In addition, defects in IFNGR1 are a cause of mendelian susceptibility to mycobacterial disease, also known as familial disseminated atypical mycobacterial infection. [provided by RefSeq, Jul 2008]
Gene Name: Interferon Gamma Receptor 1
Chromosome: CHR6: 137518620 -137540567
Locus: 6q23.3
SMCHD1 Gene Summary
This gene encodes a protein which contains a hinge region domain found in members of the SMC (structural maintenance of chromosomes) protein family. [provided by RefSeq, Dec 2011]
Gene Name: Structural Maintenance Of Chromosomes Flexible Hinge Domain Containing 1
Chromosome: CHR18: 2655885 -2805015
Locus: 18p11.32
Gene Diseases
The IFNGR1 SMCHD1 Fusion has been associated with the following diseases:
| Disease Name |
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| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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