HSA404617 FISH Probe
The HSA404617 FISH probe is designed to hybridize to the HSA404617 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 |
|---|---|---|---|---|
| KCNQ1DN-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| KCNQ1DN-20-RE | 20 (40 μL) | 200 μL |  |
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| KCNQ1DN-20-GO | 20 (40 μL) | 200 μL |  |
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| KCNQ1DN-20-GR | 20 (40 μL) | 200 μL |  |
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| KCNQ1DN-20-AQ | 20 (40 μL) | 200 μL |  |
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| KCNQ1DN-20-DIG | 20 (40 μL) | 200 μL |  |
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| KCNQ1DN-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Summary
Imprinting is a phenomenon in which epigenetic modifications lead to expression or suppression of alleles of some genes based on their parental origin. Wilms tumor-2 (WT2; MIM 194071) is defined by maternal-specific loss of heterozygosity of a critical region on chromosome 11p15.5 that includes several imprinted genes. KCNQ1DN is an imprinted gene located within the WT2 critical region that is expressed from the maternal allele (Xin et al., 2000 [PubMed 11056398]).[supplied by OMIM, Mar 2008]
Gene Details
Gene Symbol: KCNQ1DN
Gene Name: KCNQ1 Downstream Neighbor (non-protein Coding)
Chromosome: CHR11: 2891262-2893336
Locus: 11p15.5
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: HSA404617 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: KCNQ1DN-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping