RBCK1-CLCN7 Fusion FISH Probe
The RBCK1-CLCN7 Fusion FISH Probe is used to confirm a fusion of the RBCK1 and CLCN7 genes. The fusion of the RBCK1 and CLCN7 genes has been associated with Colon Adenocarcinoma. 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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| RBCK1-CLCN7-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-RERE | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-REOR | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-REGO | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-REGR | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-REAQ | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-ORRE | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-OROR | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-ORGO | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-ORAQ | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-GORE | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-GOOR | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-GOGO | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-GOGR | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-GOAQ | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-GRRE | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-GROR | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-GRGO | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-GRGR | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-GRAQ | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-AQRE | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-AQOR | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-AQGO | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-AQGR | 20 (40 μL) | 200 μL |
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| RBCK1-CLCN7-20-AQAQ | 20 (40 μL) | 200 μL |
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CLCN7 Gene Summary
The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood. [provided by RefSeq, Jul 2008]
Gene Name: Chloride Voltage-gated Channel 7
Chromosome: CHR16: 1494934 -1525085
Locus: 16p13.3
RBCK1 Gene Summary
The protein encoded by this gene is similar to mouse UIP28/UbcM4 interacting protein. Alternative splicing has been observed at this locus, resulting in distinct isoforms. [provided by RefSeq, Jul 2008]
Gene Name: RANBP2-type And C3HC4-type Zinc Finger Containing 1
Chromosome: CHR20: 388708 -411610
Locus: 20p13
Gene Diseases
The RBCK1 CLCN7 Fusion has been associated with the following diseases:
| Disease Name |
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| Colon Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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