CHD8-KIAA1211 Fusion FISH Probe
The CHD8-KIAA1211 Fusion FISH Probe is used to confirm a fusion of the CHD8 and KIAA1211 genes. The fusion of the CHD8 and KIAA1211 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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| CHD8-KIAA1211-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-RERE | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-REOR | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-REGO | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-REGR | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-REAQ | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-ORRE | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-OROR | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-ORGO | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-ORAQ | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-GORE | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-GOOR | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-GOGO | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-GOGR | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-GOAQ | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-GRRE | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-GROR | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-GRGO | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-GRGR | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-GRAQ | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-AQRE | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-AQOR | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-AQGO | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-AQGR | 20 (40 μL) | 200 μL |
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| CHD8-KIAA1211-20-AQAQ | 20 (40 μL) | 200 μL |
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KIAA1211 Gene Summary
The (KIAA1211) gene is located on chr4 :57036360-57196890 at 4q12.
Gene Name:
Chromosome: CHR4: 57036360 -57196890
Locus: 4q12
CHD8 Gene Summary
This gene encodes a member of the chromodomain-helicase-DNA binding protein family, which is characterized by a SNF2-like domain and two chromatin organization modifier domains. The encoded protein also contains brahma and kismet domains, which are common to the subfamily of chromodomain-helicase-DNA binding proteins to which this protein belongs. This gene has been shown to function in several processes that include transcriptional regulation, epigenetic remodeling, promotion of cell proliferation, and regulation of RNA synthesis. Allelic variants of this gene are associated with autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2016]
Gene Name: Chromodomain Helicase DNA Binding Protein 8
Chromosome: CHR14: 21853352 -21905457
Locus: 14q11.2
Gene Diseases
The CHD8 KIAA1211 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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