RCCD1-BLM Fusion FISH Probe
The RCCD1-BLM Fusion FISH Probe is used to confirm a fusion of the RCCD1 and BLM genes. The fusion of the RCCD1 and BLM genes has been associated with Lung 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. 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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| RCCD1-BLM-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-RERE | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-REOR | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-REGO | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-REGR | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-REAQ | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-ORRE | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-OROR | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-ORGO | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-ORAQ | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-GORE | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-GOOR | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-GOGO | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-GOGR | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-GOAQ | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-GRRE | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-GROR | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-GRGO | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-GRGR | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-GRAQ | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-AQRE | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-AQOR | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-AQGO | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-AQGR | 20 (40 μL) | 200 μL |
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| RCCD1-BLM-20-AQAQ | 20 (40 μL) | 200 μL |
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BLM Gene Summary
The Bloom syndrome gene product is related to the RecQ subset of DExH box-containing DNA helicases and has both DNA-stimulated ATPase and ATP-dependent DNA helicase activities. Mutations causing Bloom syndrome delete or alter helicase motifs and may disable the 3'-5' helicase activity. The normal protein may act to suppress inappropriate recombination. [provided by RefSeq, Jul 2008]
Gene Name: Bloom Syndrome RecQ Like Helicase
Chromosome: CHR15: 91260578 -91358686
Locus: 15q26.1
RCCD1 Gene Summary
The RCC1 Domain Containing 1 (RCCD1) gene is located on chr15 :91498105-91506355 at 15q26.1.
Gene Name: RCC1 Domain Containing 1
Chromosome: CHR15: 91498105 -91506355
Locus: 15q26.1
Gene Diseases
The RCCD1 BLM Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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