ATP2B1-DCDC2 Fusion FISH Probe
The ATP2B1-DCDC2 Fusion FISH Probe is used to confirm a fusion of the ATP2B1 and DCDC2 genes. The fusion of the ATP2B1 and DCDC2 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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| ATP2B1-DCDC2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-RERE | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-REOR | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-REGO | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-REGR | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-REAQ | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-ORRE | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-OROR | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-ORGO | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-ORAQ | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-GORE | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-GOOR | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-GOGO | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-GOGR | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-GOAQ | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-GRRE | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-GROR | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-GRGO | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-GRGR | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-GRAQ | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-AQRE | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-AQOR | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-AQGO | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-AQGR | 20 (40 μL) | 200 μL |
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| ATP2B1-DCDC2-20-AQAQ | 20 (40 μL) | 200 μL |
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ATP2B1 Gene Summary
The protein encoded by this gene belongs to the family of P-type primary ion transport ATPases characterized by the formation of an aspartyl phosphate intermediate during the reaction cycle. These enzymes remove bivalent calcium ions from eukaryotic cells against very large concentration gradients and play a critical role in intracellular calcium homeostasis. The mammalian plasma membrane calcium ATPase isoforms are encoded by at least four separate genes and the diversity of these enzymes is further increased by alternative splicing of transcripts. The expression of different isoforms and splice variants is regulated in a developmental, tissue- and cell type-specific manner, suggesting that these pumps are functionally adapted to the physiological needs of particular cells and tissues. This gene encodes the plasma membrane calcium ATPase isoform 1. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Gene Name: ATPase Plasma Membrane Ca2+ Transporting 1
Chromosome: CHR12: 89981825 -90049844
Locus: 12q21.33
DCDC2 Gene Summary
This gene encodes a doublecortin domain-containing family member. The doublecortin domain has been demonstrated to bind tubulin and enhance microtubule polymerization. This family member is thought to function in neuronal migration where it may affect the signaling of primary cilia. Mutations in this gene have been associated with reading disability (RD) type 2, also referred to as developmental dyslexia. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2013]
Gene Name: Doublecortin Domain Containing 2
Chromosome: CHR6: 24171982 -24383520
Locus: 6p22.3
Gene Diseases
The ATP2B1 DCDC2 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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