LMBRD1-LGSN Fusion FISH Probe
The LMBRD1-LGSN Fusion FISH Probe is used to confirm a fusion of the LMBRD1 and LGSN genes. The fusion of the LMBRD1 and LGSN genes has been associated with Thyroid 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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| LMBRD1-LGSN-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-RERE | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-REOR | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-REGO | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-REGR | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-REAQ | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-ORRE | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-OROR | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-ORGO | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-ORAQ | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-GORE | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-GOOR | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-GOGO | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-GOGR | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-GOAQ | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-GRRE | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-GROR | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-GRGO | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-GRGR | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-GRAQ | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-AQRE | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-AQOR | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-AQGO | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-AQGR | 20 (40 μL) | 200 μL |
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| LMBRD1-LGSN-20-AQAQ | 20 (40 μL) | 200 μL |
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LGSN Gene Summary
This gene encodes a protein with similarity to the GS I members of the glutamine synthetase superfamily. The encoded protein is referred to as a pseudo-glutamine synthetase because it has no glutamine synthesis activity and may function as a chaperone protein. This protein is localized to the lens and may be associated with cataract disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2009]
Gene Name: Lengsin, Lens Protein With Glutamine Synthetase Domain
Chromosome: CHR6: 63985855 -64029882
Locus: 6q12
LMBRD1 Gene Summary
This gene encodes a lysosomal membrane protein that may be involved in the transport and metabolism of cobalamin. This protein also interacts with the large form of the hepatitis delta antigen and may be required for the nucleocytoplasmic shuttling of the hepatitis delta virus. Mutations in this gene are associated with the vitamin B12 metabolism disorder termed, homocystinuria-megaloblastic anemia complementation type F.[provided by RefSeq, Oct 2009]
Gene Name: LMBR1 Domain Containing 1
Chromosome: CHR6: 70385640 -70507049
Locus: 6q13
Gene Diseases
The LMBRD1 LGSN Fusion has been associated with the following diseases:
| Disease Name |
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| Thyroid Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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