INSIGF FISH Probe
The INSIGF FISH probe is designed to hybridize to the INSIGF gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.
** 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 |
|---|---|---|---|---|
| INS-IGF2-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| INS-IGF2-20-RE | 20 (40 μL) | 200 μL |  |
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| INS-IGF2-20-GO | 20 (40 μL) | 200 μL |  |
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| INS-IGF2-20-GR | 20 (40 μL) | 200 μL |  |
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| INS-IGF2-20-AQ | 20 (40 μL) | 200 μL |  |
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| INS-IGF2-20-DIG | 20 (40 μL) | 200 μL |  |
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| INS-IGF2-20-BIO | 20 (40 μL) | 200 μL |  |
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: INSIGF 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