HMG20A-RCN2 Fusion FISH Probe
The HMG20A-RCN2 Fusion FISH Probe is used to confirm a fusion of the HMG20A and RCN2 genes. The fusion of the HMG20A and RCN2 genes has been associated with Lung 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| HMG20A-RCN2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-RERE | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-REOR | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-REGO | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-REGR | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-REAQ | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-ORRE | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-OROR | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-ORGO | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-ORAQ | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-GORE | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-GOOR | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-GOGO | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-GOGR | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-GOAQ | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-GRRE | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-GROR | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-GRGO | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-GRGR | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-GRAQ | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-AQRE | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-AQOR | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-AQGO | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-AQGR | 20 (40 μL) | 200 μL |
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| HMG20A-RCN2-20-AQAQ | 20 (40 μL) | 200 μL |
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RCN2 Gene Summary
The protein encoded by this gene is a calcium-binding protein located in the lumen of the ER. The protein contains six conserved regions with similarity to a high affinity Ca(+2)-binding motif, the EF-hand. This gene maps to the same region as type 4 Bardet-Biedl syndrome, suggesting a possible causative role for this gene in the disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2012]
Gene Name: Reticulocalbin 2
Chromosome: CHR15: 77223961 -77242601
Locus: 15q24.3
HMG20A Gene Summary
The High Mobility Group 20A (HMG20A) gene is located on chr15 :77713242-77777945 at 15q24.3.
Gene Name: High Mobility Group 20A
Chromosome: CHR15: 77713242 -77777945
Locus: 15q24.3
Gene Diseases
The HMG20A RCN2 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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