EPB41-ITPR1 Fusion FISH Probe
The EPB41-ITPR1 Fusion FISH Probe is used to confirm a fusion of the EPB41 and ITPR1 genes. The fusion of the EPB41 and ITPR1 genes has been associated with Skin Cutaneous Melanoma. 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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| EPB41-ITPR1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-RERE | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-REOR | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-REGO | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-REGR | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-REAQ | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-ORRE | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-OROR | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-ORGO | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-ORAQ | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-GORE | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-GOOR | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-GOGO | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-GOGR | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-GOAQ | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-GRRE | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-GROR | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-GRGO | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-GRGR | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-GRAQ | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-AQRE | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-AQOR | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-AQGO | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-AQGR | 20 (40 μL) | 200 μL |
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| EPB41-ITPR1-20-AQAQ | 20 (40 μL) | 200 μL |
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EPB41 Gene Summary
The protein encoded by this gene, together with spectrin and actin, constitute the red cell membrane cytoskeletal network. This complex plays a critical role in erythrocyte shape and deformability. Mutations in this gene are associated with type 1 elliptocytosis (EL1). Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Oct 2009]
Gene Name: Erythrocyte Membrane Protein Band 4.1
Chromosome: CHR1: 29213602 -29446558
Locus: 1p35.3
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
Gene Diseases
The EPB41 ITPR1 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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