PBRM1-GLT8D1 Fusion FISH Probe
The PBRM1-GLT8D1 Fusion FISH Probe is used to confirm a fusion of the PBRM1 and GLT8D1 genes. The fusion of the PBRM1 and GLT8D1 genes has been associated with Head And Neck Squamous Cell 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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PBRM1-GLT8D1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-RERE | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-REOR | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-REGO | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-REGR | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-REAQ | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-ORRE | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-OROR | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-ORGO | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-ORAQ | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-GORE | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-GOOR | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-GOGO | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-GOGR | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-GOAQ | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-GRRE | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-GROR | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-GRGO | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-GRGR | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-GRAQ | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-AQRE | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-AQOR | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-AQGO | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-AQGR | 20 (40 μL) | 200 μL | ||
PBRM1-GLT8D1-20-AQAQ | 20 (40 μL) | 200 μL |
PBRM1 Gene Summary
This locus encodes a subunit of ATP-dependent chromatin-remodeling complexes. The encoded protein has been identified as in integral component of complexes necessary for ligand-dependent transcriptional activation by nuclear hormone receptors. Mutations at this locus have been associated with primary clear cell renal cell carcinoma. [provided by RefSeq, Feb 2012]
Gene Name: Polybromo 1
Chromosome: CHR3: 52579367 -52719866
Locus: 3p21.1
GLT8D1 Gene Summary
This gene encodes a member of the glycosyltransferase family. The specific function of this protein has not been determined. Alternative splicing results in multiple transcript variants of this gene [provided by RefSeq, May 2013]
Gene Name: Glycosyltransferase 8 Domain Containing 1
Chromosome: CHR3: 52728503 -52740048
Locus: 3p21.1
Gene Diseases
The PBRM1 GLT8D1 Fusion has been associated with the following diseases:
Disease Name |
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Head And Neck Squamous Cell Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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