ITPR1-SUMF1 Fusion FISH Probe
The ITPR1-SUMF1 Fusion FISH Probe is used to confirm a fusion of the ITPR1 and SUMF1 genes. The fusion of the ITPR1 and SUMF1 genes has been associated with Lung Squamous Cell 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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| ITPR1-SUMF1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-RERE | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-REOR | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-REGO | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-REGR | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-REAQ | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-ORRE | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-OROR | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-ORGO | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-ORAQ | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-GORE | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-GOOR | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-GOGO | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-GOGR | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-GOAQ | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-GRRE | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-GROR | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-GRGO | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-GRGR | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-GRAQ | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-AQRE | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-AQOR | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-AQGO | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-AQGR | 20 (40 μL) | 200 μL |
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| ITPR1-SUMF1-20-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
SUMF1 Gene Summary
This gene encodes an enzyme that catalyzes the hydrolysis of sulfate esters by oxidizing a cysteine residue in the substrate sulfatase to an active site 3-oxoalanine residue, which is also known as C-alpha-formylglycine. Mutations in this gene cause multiple sulfatase deficiency, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
Gene Name: Sulfatase Modifying Factor 1
Chromosome: CHR3: 4402828 -4508966
Locus: 3p26.1
Gene Diseases
The ITPR1 SUMF1 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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