ST3GAL3-GLCCI1 Fusion FISH Probe
The ST3GAL3-GLCCI1 Fusion FISH Probe is used to confirm a fusion of the ST3GAL3 and GLCCI1 genes. The fusion of the ST3GAL3 and GLCCI1 genes has been associated with Pheochromocytoma And Paraganglioma. 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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| ST3GAL3-GLCCI1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-RERE | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-REOR | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-REGO | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-REGR | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-REAQ | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-ORRE | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-OROR | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-ORGO | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-ORAQ | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-GORE | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-GOOR | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-GOGO | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-GOGR | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-GOAQ | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-GRRE | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-GROR | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-GRGO | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-GRGR | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-GRAQ | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-AQRE | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-AQOR | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-AQGO | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-AQGR | 20 (40 μL) | 200 μL |
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| ST3GAL3-GLCCI1-20-AQAQ | 20 (40 μL) | 200 μL |
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ST3GAL3 Gene Summary
The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein is normally found in the Golgi apparatus but can be proteolytically processed to a soluble form. This protein is a member of glycosyltransferase family 29. Mutations in this gene have been associated with a form of autosomal recessive nonsymdromic cognitive disability as well as infantile epileptic encephalopathy. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]
Gene Name: ST3 Beta-galactoside Alpha-2,3-sialyltransferase 3
Chromosome: CHR1: 44173217 -44396831
Locus: 1p34.1
GLCCI1 Gene Summary
This gene encodes a protein of unknown function. Expression of this gene is induced by glucocorticoids and may be an early marker for glucocorticoid-induced apoptosis. Single nucleotide polymorphisms in this gene are associated with a decreased response to inhaled glucocorticoids in asthmatic patients. [provided by RefSeq, Feb 2012]
Gene Name: Glucocorticoid Induced 1
Chromosome: CHR7: 8008422 -8128709
Locus: 7p21.3
Gene Diseases
The ST3GAL3 GLCCI1 Fusion has been associated with the following diseases:
| Disease Name |
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| Pheochromocytoma And Paraganglioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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