PRODUCTS
ZytoLight ® SPEC DiGeorge/Phelan McDermid Dual Color Probe
The ZytoLight ® SPEC DiGeorge/Phelan McDermid Dual Color Probe is designed to detect deletions affecting the chromosomal regions 22q11.21 harboring the HIRA (a.k.a. TUPLE1) gene and 22q13.33 harboring the SHANK3 gene, respectively. The 22q13.3 deletion syndrome (Phelan McDermid syndrome) typically results from deletions of 100 kb to 9 Mb involving the distal long arm of chromosome 22. Almost all of these deletions include the SHANK 3 gene.
Probe Maps
Ordering Information
| Prod. No.: | Tests¹ (Volume): | Intended Use²: | ||
|---|---|---|---|---|
| Z-2299-50 |
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Download Information
| 1 | Using 10 μl probe solution per test. |
| 2 | In vitro diagnostic medical device according to EU directive 98/79/EC. CE IVD only available in certain countries. All other countries research use only! Please contact your local dealer for more information. |
