ALG12-FAM116B Fusion FISH Probe
The ALG12-FAM116B Fusion FISH Probe is used to confirm a fusion of the ALG12 and FAM116B genes. The fusion of the ALG12 and FAM116B genes has been associated with Uterine Carcinosarcoma. 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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| ALG12-FAM116B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-RERE | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-REOR | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-REGO | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-REGR | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-REAQ | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-ORRE | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-OROR | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-ORGO | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-ORAQ | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-GORE | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-GOOR | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-GOGO | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-GOGR | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-GOAQ | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-GRRE | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-GROR | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-GRGO | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-GRGR | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-GRAQ | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-AQRE | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-AQOR | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-AQGO | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-AQGR | 20 (40 μL) | 200 μL |
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| ALG12-FAM116B-20-AQAQ | 20 (40 μL) | 200 μL |
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ALG12 Gene Summary
This gene encodes a member of the glycosyltransferase 22 family. The encoded protein catalyzes the addition of the eighth mannose residue in an alpha-1,6 linkage onto the dolichol-PP-oligosaccharide precursor (dolichol-PP-Man(7)GlcNAc(2)) required for protein glycosylation. Mutations in this gene have been associated with congenital disorder of glycosylation type Ig (CDG-Ig)characterized by abnormal N-glycosylation. [provided by RefSeq, Jul 2008]
Gene Name: ALG12, Alpha-1,6-mannosyltransferase
Chromosome: CHR22: 50296853 -50312106
Locus: 22q13.33
Gene Diseases
The ALG12 FAM116B Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Carcinosarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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