FAM83G-B9D1 Fusion FISH Probe
The FAM83G-B9D1 Fusion FISH Probe is used to confirm a fusion of the FAM83G and B9D1 genes. The fusion of the FAM83G and B9D1 genes has been associated with Esophageal Carcinoma. 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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| FAM83G-B9D1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-RERE | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-REOR | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-REGO | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-REGR | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-REAQ | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-ORRE | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-OROR | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-ORGO | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-ORAQ | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-GORE | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-GOOR | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-GOGO | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-GOGR | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-GOAQ | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-GRRE | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-GROR | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-GRGO | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-GRGR | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-GRAQ | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-AQRE | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-AQOR | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-AQGO | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-AQGR | 20 (40 μL) | 200 μL |
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| FAM83G-B9D1-20-AQAQ | 20 (40 μL) | 200 μL |
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B9D1 Gene Summary
This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Mar 2016]
Gene Name: B9 Domain Containing 1
Chromosome: CHR17: 19240866 -19281495
Locus: 17p11.2
FAM83G Gene Summary
The Family With Sequence Similarity 83 Member G (FAM83G) gene is located on chr17 :18874380-18908060 at 17p11.2.
Gene Name: Family With Sequence Similarity 83 Member G
Chromosome: CHR17: 18874380 -18908060
Locus: 17p11.2
Gene Diseases
The FAM83G B9D1 Fusion has been associated with the following diseases:
| Disease Name |
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| Esophageal Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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