INS-IGF2 Break Apart FISH Probe
Empire Genomics’ INS-IGF2 Break Apart FISH Probe is designed to flank the INS-IGF2 gene and is typically used for detecting INS-IGF2 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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| INS-IGF2BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| INS-IGF2BA-20-AQOR | 20 (40 μL) | 200 μL |
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| INS-IGF2BA-20-GOGR | 20 (40 μL) | 200 μL |
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| INS-IGF2BA-20-GORE | 20 (40 μL) | 200 μL |
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| INS-IGF2BA-20-GRGO | 20 (40 μL) | 200 μL |
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| INS-IGF2BA-20-GRRE | 20 (40 μL) | 200 μL |
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| INS-IGF2BA-20-ORGR | 20 (40 μL) | 200 μL |
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| INS-IGF2BA-20-REGO | 20 (40 μL) | 200 μL |
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| INS-IGF2BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This locus includes two alternatively spliced read-through transcript variants which align to the INS gene in the 5' region and to the IGF2 gene in the 3' region. One transcript is predicted to encode a protein which shares the N-terminus with the INS protein but has a distinct and longer C-terminus, whereas the other transcript is a candidate for nonsense-mediated decay (NMD). The transcripts are imprinted and are paternally expressed in the limb and eye. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: INS-IGF2
Gene Name: INS-IGF2 Readthrough
Chromosome: CHR11: 2150341-2182439
Locus: 11p15.5
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: INS-IGF2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: INS-IGF2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping