w10.0.26 | c9.0.88.80
PROD | u7.5.14
 

 

Frequently Asked Questions About Our Products And Services


starting material

For information on the quantity and concentration required for specific library preparation methods please refer to your quote or contact us. For optimum results, we generally require >10 ng of double-stranded, purified DNA for PCR amplification (the total amount depends on the proportion of microbial DNA in the sample). Moreover, the DNA has to be RNA-free with an OD 260/280 of >1.8 and OD 260/230 of >1.9.

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