AZIN1-ITPR1 Fusion FISH Probe
The AZIN1-ITPR1 Fusion FISH Probe is used to confirm a fusion of the AZIN1 and ITPR1 genes. The fusion of the AZIN1 and ITPR1 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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| AZIN1-ITPR1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-RERE | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-REOR | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-REGO | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-REGR | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-REAQ | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-ORRE | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-OROR | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-ORGO | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-ORAQ | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-GORE | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-GOOR | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-GOGO | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-GOGR | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-GOAQ | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-GRRE | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-GROR | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-GRGO | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-GRGR | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-GRAQ | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-AQRE | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-AQOR | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-AQGO | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-AQGR | 20 (40 μL) | 200 μL |
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| AZIN1-ITPR1-20-AQAQ | 20 (40 μL) | 200 μL |
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ITPR1 Gene Summary
This gene encodes an intracellular receptor for inositol 1,4,5-trisphosphate. Upon stimulation by inositol 1,4,5-trisphosphate, this receptor mediates calcium release from the endoplasmic reticulum. Mutations in this gene cause spinocerebellar ataxia type 15, a disease associated with an heterogeneous group of cerebellar disorders. Multiple transcript variants have been identified for this gene. [provided by RefSeq, Nov 2009]
Gene Name: Inositol 1,4,5-trisphosphate Receptor Type 1
Chromosome: CHR3: 4535031 -4889524
Locus: 3p26.1
AZIN1 Gene Summary
The protein encoded by this gene belongs to the antizyme inhibitor family, which plays a role in cell growth and proliferation by maintaining polyamine homeostasis within the cell. Antizyme inhibitors are homologs of ornithine decarboxylase (ODC, the key enzyme in polyamine biosynthesis) that have lost the ability to decarboxylase ornithine; however, retain the ability to bind to antizymes. Antizymes negatively regulate intracellular polyamine levels by binding to ODC and targeting it for degradation, as well as by inhibiting polyamine uptake. Antizyme inhibitors function as positive regulators of polyamine levels by sequestering antizymes and neutralizing their effect. This gene encodes antizyme inhibitor 1, the first member of this gene family that is ubiquitously expressed, and is localized in the nucleus and cytoplasm. Overexpression of antizyme inhibitor 1 gene has been associated with increased proliferation, cellular transformation and tumorigenesis. Gene knockout studies showed that homozygous mutant mice lacking functional antizyme inhibitor 1 gene died at birth with abnormal liver morphology. RNA editing of this gene, predominantly in the liver tissue, has been linked to the progression of hepatocellular carcinoma. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Sep 2014]
Gene Name: Antizyme Inhibitor 1
Chromosome: CHR8: 103838535 -103876397
Locus: 8q22.3
Gene Diseases
The AZIN1 ITPR1 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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