DEPDC1B-ERCC8 Fusion FISH Probe
The DEPDC1B-ERCC8 Fusion FISH Probe is used to confirm a fusion of the DEPDC1B and ERCC8 genes. The fusion of the DEPDC1B and ERCC8 genes has been associated with Stomach 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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| DEPDC1B-ERCC8-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-RERE | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-REOR | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-REGO | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-REGR | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-REAQ | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-ORRE | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-OROR | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-ORGO | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-ORAQ | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-GORE | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-GOOR | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-GOGO | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-GOGR | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-GOAQ | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-GRRE | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-GROR | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-GRGO | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-GRGR | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-GRAQ | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-AQRE | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-AQOR | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-AQGO | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-AQGR | 20 (40 μL) | 200 μL |
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| DEPDC1B-ERCC8-20-AQAQ | 20 (40 μL) | 200 μL |
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ERCC8 Gene Summary
This gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014]
Gene Name: ERCC Excision Repair 8, CSA Ubiquitin Ligase Complex Subunit
Chromosome: CHR5: 60169658 -60240905
Locus: 5q12.1
DEPDC1B Gene Summary
The DEP Domain Containing 1B (DEPDC1B) gene is located on chr5 :59892738-59995993 at 5q12.1.
Gene Name: DEP Domain Containing 1B
Chromosome: CHR5: 59892738 -59995993
Locus: 5q12.1
Gene Diseases
The DEPDC1B ERCC8 Fusion has been associated with the following diseases:
| Disease Name |
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| Stomach Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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