GTF2IRD2 Break Apart FISH Probe
Empire Genomics’ GTF2IRD2 Break Apart FISH Probe is designed to flank the GTF2IRD2 gene and is typically used for detecting GTF2IRD2 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange by default, but may be customized to meet your needs.
** 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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| GTF2IRD2BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| GTF2IRD2BA-20-AQOR | 20 (40 μL) | 200 μL |
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| GTF2IRD2BA-20-GOGR | 20 (40 μL) | 200 μL |
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| GTF2IRD2BA-20-GORE | 20 (40 μL) | 200 μL |
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| GTF2IRD2BA-20-GRGO | 20 (40 μL) | 200 μL |
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| GTF2IRD2BA-20-GRRE | 20 (40 μL) | 200 μL |
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| GTF2IRD2BA-20-ORGR | 20 (40 μL) | 200 μL |
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| GTF2IRD2BA-20-REGO | 20 (40 μL) | 200 μL |
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| GTF2IRD2BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene is one of several closely related genes on chromosome 7 encoding proteins containing helix-loop-helix motifs. These proteins may function as regulators of transcription. The encoded protein is unique in that its C-terminus is derived from CHARLIE8 transposable element sequence. This gene is located in a region of chromosome 7 that is deleted in Williams-Beuren syndrome, and loss of this locus may contribute to the cognitive phenotypes observed in this disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
Gene Details
Gene Symbol: GTF2IRD2
Gene Name: GTF2I Repeat Domain Containing 2
Chromosome: CHR7: 74210483-74267841
Locus: 7q11.23
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: GTF2IRD2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: GTF2IRD2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping