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Mapping 250K/500K SNP assay

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112 GeneChip ® <strong>Mapping</strong> <strong>500K</strong> Assay Manual<br />

Reagent Volume/Rx<br />

Fragmented DNA<br />

(less the 4 µL used for gel analysis)<br />

3. Seal the plate tightly with adhesive film.<br />

4. Vortex the center of the plate at high speed for 3 sec.<br />

5. Spin down the plate at 2000 rpm for 30 sec.<br />

50.5 µL<br />

Labeling Mix 19.5 µL<br />

Total 70 µL<br />

Check to ensure that the plate is tightly sealed, particularly around<br />

the wells on the edge of the plate. The plate must be tightly sealed<br />

to minimize evaporation while on the thermal cycler.<br />

6. Place the plate on the pre-heated thermal cycler block, and run the<br />

<strong>500K</strong> Label program.<br />

Samples can remain at 4 °C overnight.<br />

<strong>500K</strong> Label Program<br />

Temperature Time<br />

37ºC 4 hours<br />

95ºC 15 minutes<br />

4ºC Hold<br />

Samples can remain at 4 °C overnight.<br />

7. When the <strong>500K</strong> Labeling program is finished:<br />

A. Remove the plate from the thermal cycler.<br />

B. Spin down the plate at 2000 rpm for 30 sec.

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