EPB41-HGSNAT Fusion FISH Probe
The EPB41-HGSNAT Fusion FISH Probe is used to confirm a fusion of the EPB41 and HGSNAT genes. The fusion of the EPB41 and HGSNAT genes has been associated with Bladder Urothelial 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| EPB41-HGSNAT-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-RERE | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-REOR | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-REGO | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-REGR | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-REAQ | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-ORRE | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-OROR | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-ORGO | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-ORAQ | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-GORE | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-GOOR | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-GOGO | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-GOGR | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-GOAQ | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-GRRE | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-GROR | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-GRGO | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-GRGR | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-GRAQ | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-AQRE | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-AQOR | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-AQGO | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-20-AQGR | 20 (40 μL) | 200 μL |
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| EPB41-HGSNAT-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
HGSNAT Gene Summary
This gene encodes a lysosomal acetyltransferase, which is one of several enzymes involved in the lysosomal degradation of heparin sulfate. Mutations in this gene are associated with Sanfilippo syndrome C, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. [provided by RefSeq, Jan 2009]
Gene Name: Heparan-alpha-glucosaminide N-acetyltransferase
Chromosome: CHR8: 42995591 -43057970
Locus: 8p11.21-p11.1
Gene Diseases
The EPB41 HGSNAT Fusion has been associated with the following diseases:
| Disease Name |
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| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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