ERCC2-C12ORF40 Fusion FISH Probe
The ERCC2-C12ORF40 Fusion FISH Probe is used to confirm a fusion of the ERCC2 and C12ORF40 genes. The fusion of the ERCC2 and C12ORF40 genes has been associated with Brain Lower Grade Glioma. 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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| ERCC2-C12ORF40-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-RERE | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-REOR | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-REGO | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-REGR | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-REAQ | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-ORRE | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-OROR | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-ORGO | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-ORAQ | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-GORE | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-GOOR | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-GOGO | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-GOGR | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-GOAQ | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-GRRE | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-GROR | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-GRGO | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-GRGR | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-GRAQ | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-AQRE | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-AQOR | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-AQGO | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-AQGR | 20 (40 μL) | 200 μL |
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| ERCC2-C12ORF40-20-AQAQ | 20 (40 μL) | 200 μL |
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ERCC2 Gene Summary
The nucleotide excision repair pathway is a mechanism to repair damage to DNA. The protein encoded by this gene is involved in transcription-coupled nucleotide excision repair and is an integral member of the basal transcription factor BTF2/TFIIH complex. The gene product has ATP-dependent DNA helicase activity and belongs to the RAD3/XPD subfamily of helicases. Defects in this gene can result in three different disorders, the cancer-prone syndrome xeroderma pigmentosum complementation group D, trichothiodystrophy, and Cockayne syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]
Gene Name: ERCC Excision Repair 2, TFIIH Core Complex Helicase Subunit
Chromosome: CHR19: 45854648 -45873845
Locus: 19q13.32
C12orf40 Gene Summary
The Chromosome 12 Open Reading Frame 40 (C12orf40) gene is located on chr12 :40019971-40115720 at 12q12.
Gene Name: Chromosome 12 Open Reading Frame 40
Chromosome: CHR12: 40019971 -40115720
Locus: 12q12
Gene Diseases
The ERCC2 C12ORF40 Fusion has been associated with the following diseases:
| Disease Name |
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| Brain Lower Grade Glioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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