CAPN1-GTF2IRD1 Fusion FISH Probe
The CAPN1-GTF2IRD1 Fusion FISH Probe is used to confirm a fusion of the CAPN1 and GTF2IRD1 genes. The fusion of the CAPN1 and GTF2IRD1 genes has been associated with Esophageal 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| CAPN1-GTF2IRD1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-RERE | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-REOR | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-REGO | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-REGR | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-REAQ | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-ORRE | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-OROR | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-ORGO | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-ORAQ | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-GORE | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-GOOR | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-GOGO | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-GOGR | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-GOAQ | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-GRRE | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-GROR | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-GRGO | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-GRGR | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-GRAQ | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-AQRE | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-AQOR | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-AQGO | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-AQGR | 20 (40 μL) | 200 μL |
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| CAPN1-GTF2IRD1-20-AQAQ | 20 (40 μL) | 200 μL |
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CAPN1 Gene Summary
The calpains, calcium-activated neutral proteases, are nonlysosomal, intracellular cysteine proteases. The mammalian calpains include ubiquitous, stomach-specific, and muscle-specific proteins. The ubiquitous enzymes consist of heterodimers with distinct large, catalytic subunits associated with a common small, regulatory subunit. This gene encodes the large subunit of the ubiquitous enzyme, calpain 1. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]
Gene Name: Calpain 1
Chromosome: CHR11: 64948685 -64979477
Locus: 11q13.1
GTF2IRD1 Gene Summary
The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH) motif. It may have the ability to interact with other HLH-proteins and function as a transcription factor or as a positive transcriptional regulator under the control of Retinoblastoma protein. This gene plays a role in craniofacial and cognitive development and mutations have been associated with Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010]
Gene Name: GTF2I Repeat Domain Containing 1
Chromosome: CHR7: 73868119 -74016920
Locus: 7q11.23
Gene Diseases
The CAPN1 GTF2IRD1 Fusion has been associated with the following diseases:
| Disease Name |
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| Esophageal Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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