GNL3L-GABRB3 Fusion FISH Probe
The GNL3L-GABRB3 Fusion FISH Probe is used to confirm a fusion of the GNL3L and GABRB3 genes. The fusion of the GNL3L and GABRB3 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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| GNL3L-GABRB3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-RERE | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-REOR | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-REGO | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-REGR | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-REAQ | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-ORRE | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-OROR | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-ORGO | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-ORAQ | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-GORE | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-GOOR | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-GOGO | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-GOGR | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-GOAQ | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-GRRE | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-GROR | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-GRGO | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-GRGR | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-GRAQ | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-AQRE | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-AQOR | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-AQGO | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-AQGR | 20 (40 μL) | 200 μL |
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| GNL3L-GABRB3-20-AQAQ | 20 (40 μL) | 200 μL |
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GABRB3 Gene Summary
This gene encodes a member of the ligand-gated ionic channel family. The encoded protein is one the subunits of a multi-subunit chloride channel that serves as the receptor for gamma-aminobutyric acid, a major inhibitory neurotransmitter of the mammalian nervous system. This gene is located on the long arm of chromosome 15 in a cluster with two other genes encoding related subunits of the family. This gene may be associated with the pathogenesis of several disorders including Angelman syndrome, Prader-Willi syndrome, nonsyndromic orofacial clefts, epilepsy and autism. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2013]
Gene Name: Gamma-aminobutyric Acid Type A Receptor Beta3 Subunit
Chromosome: CHR15: 26788693 -27018935
Locus: 15q12
GNL3L Gene Summary
The protein encoded by this gene appears to be a nucleolar GTPase that is essential for ribosomal pre-rRNA processing and cell proliferation. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, May 2010]
Gene Name: G Protein Nucleolar 3 Like
Chromosome: CHRX: 54556643 -54593720
Locus: Xp11.22
Gene Diseases
The GNL3L GABRB3 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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