ATP2C1-C18ORF45 Fusion FISH Probe
The ATP2C1-C18ORF45 Fusion FISH Probe is used to confirm a fusion of the ATP2C1 and C18ORF45 genes. The fusion of the ATP2C1 and C18ORF45 genes has been associated with Sarcoma. 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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| ATP2C1-C18ORF45-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-RERE | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-REOR | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-REGO | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-REGR | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-REAQ | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-ORRE | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-OROR | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-ORGO | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-ORAQ | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-GORE | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-GOOR | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-GOGO | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-GOGR | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-GOAQ | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-GRRE | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-GROR | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-GRGO | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-GRGR | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-GRAQ | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-AQRE | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-AQOR | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-AQGO | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-AQGR | 20 (40 μL) | 200 μL |
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| ATP2C1-C18ORF45-20-AQAQ | 20 (40 μL) | 200 μL |
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ATP2C1 Gene Summary
The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium ions. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]
Gene Name: ATPase Secretory Pathway Ca2+ Transporting 1
Chromosome: CHR3: 130569368 -130735555
Locus: 3q22.1
Gene Diseases
The ATP2C1 C18ORF45 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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