NEO1-BBS4 Fusion FISH Probe
The NEO1-BBS4 Fusion FISH Probe is used to confirm a fusion of the NEO1 and BBS4 genes. The fusion of the NEO1 and BBS4 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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| NEO1-BBS4-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-RERE | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-REOR | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-REGO | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-REGR | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-REAQ | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-ORRE | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-OROR | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-ORGO | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-ORAQ | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-GORE | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-GOOR | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-GOGO | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-GOGR | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-GOAQ | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-GRRE | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-GROR | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-GRGO | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-GRGR | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-GRAQ | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-AQRE | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-AQOR | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-AQGO | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-AQGR | 20 (40 μL) | 200 μL |
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| NEO1-BBS4-20-AQAQ | 20 (40 μL) | 200 μL |
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BBS4 Gene Summary
This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse. The similar phenotypes exhibited by mutations in BBS gene family members are likely due to the protein's shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene has sequence similarity to O-linked N-acetylglucosamine (O-GlcNAc) transferases in plants and archaebacteria and in human forms a multi-protein "BBSome" complex with seven other BBS proteins. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]
Gene Name: Bardet-Biedl Syndrome 4
Chromosome: CHR15: 72978525 -73030817
Locus: 15q24.1
NEO1 Gene Summary
This gene encodes a cell surface protein that is a member of the immunoglobulin superfamily. The encoded protein consists of four N-terminal immunoglobulin-like domains, six fibronectin type III domains, a transmembrane domain and a C-terminal internal domain that shares homology with the tumor suppressor candidate gene DCC. This protein may be involved in cell growth and differentiation and in cell-cell adhesion. Defects in this gene are associated with cell proliferation in certain cancers. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]
Gene Name: Neogenin 1
Chromosome: CHR15: 73344824 -73597547
Locus: 15q24.1
Gene Diseases
The NEO1 BBS4 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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