GALNT12-ROR2 Fusion FISH Probe
The GALNT12-ROR2 Fusion FISH Probe is used to confirm a fusion of the GALNT12 and ROR2 genes. The fusion of the GALNT12 and ROR2 genes has been associated with Sarcoma. 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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| GALNT12-ROR2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-RERE | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-REOR | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-REGO | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-REGR | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-REAQ | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-ORRE | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-OROR | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-ORGO | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-ORAQ | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-GORE | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-GOOR | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-GOGO | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-GOGR | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-GOAQ | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-GRRE | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-GROR | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-GRGO | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-GRGR | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-GRAQ | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-AQRE | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-AQOR | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-AQGO | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-AQGR | 20 (40 μL) | 200 μL |
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| GALNT12-ROR2-20-AQAQ | 20 (40 μL) | 200 μL |
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ROR2 Gene Summary
The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. [provided by RefSeq, Jul 2008]
Gene Name: Receptor Tyrosine Kinase Like Orphan Receptor 2
Chromosome: CHR9: 94484877 -94712444
Locus: 9q22.31
GALNT12 Gene Summary
This gene encodes a member of a family of UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferases, which catalyze the transfer of N-acetylgalactosamine (GalNAc) from UDP-GalNAc to a serine or threonine residue on a polypeptide acceptor in the initial step of O-linked protein glycosylation. Mutations in this gene are associated with an increased susceptibility to colorectal cancer.[provided by RefSeq, Mar 2011]
Gene Name: Polypeptide N-acetylgalactosaminyltransferase 12
Chromosome: CHR9: 101569980 -101612363
Locus: 9q22.33
Gene Diseases
The GALNT12 ROR2 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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