KCNQ1DN Break Apart FISH Probe
Empire Genomics’ KCNQ1DN Break Apart FISH Probe is designed to flank the KCNQ1DN gene and is typically used for detecting KCNQ1DN rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green 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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| KCNQ1DNBA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| KCNQ1DNBA-20-AQOR | 20 (40 μL) | 200 μL |
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| KCNQ1DNBA-20-GOGR | 20 (40 μL) | 200 μL |
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| KCNQ1DNBA-20-GORE | 20 (40 μL) | 200 μL |
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| KCNQ1DNBA-20-GRGO | 20 (40 μL) | 200 μL |
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| KCNQ1DNBA-20-GROR | 20 (40 μL) | 200 μL |
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| KCNQ1DNBA-20-GRRE | 20 (40 μL) | 200 μL |
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| KCNQ1DNBA-20-REGO | 20 (40 μL) | 200 μL |
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| KCNQ1DNBA-20-REGR | 20 (40 μL) | 200 μL |
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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: KCNQ1DN 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