HMHA1-GRIN3B Fusion FISH Probe
The HMHA1-GRIN3B Fusion FISH Probe is used to confirm a fusion of the HMHA1 and GRIN3B genes. The fusion of the HMHA1 and GRIN3B genes has been associated with Cervical Squamous Cell Carcinoma And Endocervical Adenocarcinoma. 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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| HMHA1-GRIN3B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-RERE | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-REOR | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-REGO | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-REGR | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-REAQ | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-ORRE | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-OROR | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-ORGO | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-ORAQ | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-GORE | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-GOOR | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-GOGO | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-GOGR | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-GOAQ | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-GRRE | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-GROR | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-GRGO | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-GRGR | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-GRAQ | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-AQRE | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-AQOR | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-AQGO | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-AQGR | 20 (40 μL) | 200 μL |
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| HMHA1-GRIN3B-20-AQAQ | 20 (40 μL) | 200 μL |
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GRIN3B Gene Summary
The protein encoded by this gene is a subunit of an N-methyl-D-aspartate (NMDA) receptor. The encoded protein is found primarily in motor neurons, where it forms a heterotetramer with GRIN1 to create an excitatory glycine receptor. Variations in this gene have been proposed to be linked to schizophrenia. [provided by RefSeq, Nov 2015]
Gene Name: Glutamate Ionotropic Receptor NMDA Type Subunit 3B
Chromosome: CHR19: 1000436 -1009723
Locus: 19p13.3
Gene Diseases
The HMHA1 GRIN3B Fusion has been associated with the following diseases:
| Disease Name |
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| Cervical Squamous Cell Carcinoma And Endocervical Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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