CACNA2D1-NAALADL2 Fusion FISH Probe
The CACNA2D1-NAALADL2 Fusion FISH Probe is used to confirm a fusion of the CACNA2D1 and NAALADL2 genes. The fusion of the CACNA2D1 and NAALADL2 genes has been associated with Head And Neck 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| CACNA2D1-NAALADL2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-RERE | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-REOR | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-REGO | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-REGR | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-REAQ | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-ORRE | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-OROR | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-ORGO | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-ORAQ | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-GORE | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-GOOR | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-GOGO | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-GOGR | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-GOAQ | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-GRRE | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-GROR | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-GRGO | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-GRGR | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-GRAQ | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-AQRE | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-AQOR | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-AQGO | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-AQGR | 20 (40 μL) | 200 μL |
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| CACNA2D1-NAALADL2-20-AQAQ | 20 (40 μL) | 200 μL |
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CACNA2D1 Gene Summary
The preproprotein encoded by this gene is cleaved into multiple chains that comprise the alpha-2 and delta subunits of the voltage-dependent calcium channel complex. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization. Mutations in this gene can cause cardiac deficiencies, including Brugada syndrome and short QT syndrome. Alternate splicing results in multiple transcript variants, some of which may lack the delta subunit portion. [provided by RefSeq, Nov 2014]
Gene Name: Calcium Voltage-gated Channel Auxiliary Subunit Alpha2delta 1
Chromosome: CHR7: 81579417 -82073031
Locus: 7q21.11
NAALADL2 Gene Summary
The N-acetylated Alpha-linked Acidic Dipeptidase Like 2 (NAALADL2) gene is located on chr3 :174577110-175523428 at 3q26.31.
Gene Name: N-acetylated Alpha-linked Acidic Dipeptidase Like 2
Chromosome: CHR3: 174577110 -175523428
Locus: 3q26.31
Gene Diseases
The CACNA2D1 NAALADL2 Fusion has been associated with the following diseases:
| Disease Name |
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| Head And Neck Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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