B3GALNT2-LBR Fusion FISH Probe
The B3GALNT2-LBR Fusion FISH Probe is used to confirm a fusion of the B3GALNT2 and LBR genes. The fusion of the B3GALNT2 and LBR 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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| B3GALNT2-LBR-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-RERE | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-REOR | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-REGO | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-REGR | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-REAQ | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-ORRE | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-OROR | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-ORGO | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-ORAQ | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-GORE | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-GOOR | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-GOGO | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-GOGR | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-GOAQ | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-GRRE | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-GROR | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-GRGO | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-GRGR | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-GRAQ | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-AQRE | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-AQOR | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-AQGO | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-AQGR | 20 (40 μL) | 200 μL |
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| B3GALNT2-LBR-20-AQAQ | 20 (40 μL) | 200 μL |
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LBR Gene Summary
The protein encoded by this gene belongs to the ERG4/ERG24 family. It localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. It may mediate interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]
Gene Name: Lamin B Receptor
Chromosome: CHR1: 225589203 -225616557
Locus: 1q42.12
B3GALNT2 Gene Summary
This gene encodes a member of the glycosyltransferase 31 family. The encoded protein synthesizes GalNAc:beta-1,3GlcNAc, a novel carbohydrate structure, on N- and O-glycans. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Mar 2013]
Gene Name: Beta-1,3-N-acetylgalactosaminyltransferase 2
Chromosome: CHR1: 235610532 -235667781
Locus: 1q42.3
Gene Diseases
The B3GALNT2 LBR 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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