HCN2-BSG Fusion FISH Probe
The HCN2-BSG Fusion FISH Probe is used to confirm a fusion of the HCN2 and BSG genes. The fusion of the HCN2 and BSG genes has been associated with Brain Lower Grade Glioma. 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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HCN2-BSG-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-RERE | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-REOR | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-REGO | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-REGR | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-REAQ | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-ORRE | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-OROR | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-ORGO | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-ORAQ | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-GORE | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-GOOR | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-GOGO | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-GOGR | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-GOAQ | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-GRRE | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-GROR | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-GRGO | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-GRGR | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-GRAQ | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-AQRE | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-AQOR | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-AQGO | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-AQGR | 20 (40 μL) | 200 μL | ||
HCN2-BSG-20-AQAQ | 20 (40 μL) | 200 μL |
HCN2 Gene Summary
The protein encoded by this gene is a hyperpolarization-activated cation channel involved in the generation of native pacemaker activity in the heart and in the brain. The encoded protein is activated by cAMP and can produce a fast, large current. Defects in this gene were noted as a possible cause of some forms of epilepsy. [provided by RefSeq, Jan 2017]
Gene Name: Hyperpolarization Activated Cyclic Nucleotide Gated Potassium And Sodium Channel 2
Chromosome: CHR19: 589892 -617159
Locus: 19p13.3
BSG Gene Summary
The protein encoded by this gene is a plasma membrane protein that is important in spermatogenesis, embryo implantation, neural network formation, and tumor progression. The encoded protein is also a member of the immunoglobulin superfamily. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Basigin (Ok Blood Group)
Chromosome: CHR19: 571324 -583493
Locus: 19p13.3
Gene Diseases
The HCN2 BSG Fusion has been associated with the following diseases:
Disease Name |
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Brain Lower Grade Glioma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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