BBS2-C15ORF41 Fusion FISH Probe
The BBS2-C15ORF41 Fusion FISH Probe is used to confirm a fusion of the BBS2 and C15ORF41 genes. The fusion of the BBS2 and C15ORF41 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| BBS2-C15ORF41-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-RERE | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-REOR | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-REGO | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-REGR | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-REAQ | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-ORRE | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-OROR | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-ORGO | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-ORAQ | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-GORE | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-GOOR | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-GOGO | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-GOGR | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-GOAQ | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-GRRE | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-GROR | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-GRGO | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-GRGR | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-GRAQ | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-AQRE | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-AQOR | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-AQGO | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-AQGR | 20 (40 μL) | 200 μL |
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| BBS2-C15ORF41-20-AQAQ | 20 (40 μL) | 200 μL |
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BBS2 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 and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their 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 forms a multiprotein BBSome complex with seven other BBS proteins.[provided by RefSeq, Oct 2014]
Gene Name: Bardet-Biedl Syndrome 2
Chromosome: CHR16: 56518258 -56554008
Locus: 16q13
C15orf41 Gene Summary
This gene encodes a protein with two predicted helix-turn-helix domains. Mutations in this gene were found in families with congenital dyserythropoietic anemia type Ib. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]
Gene Name: Chromosome 15 Open Reading Frame 41
Chromosome: CHR15: 36871811 -37102449
Locus: 15q14
Gene Diseases
The BBS2 C15ORF41 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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