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DNase I
DNase I
Catalog #: CA10029-182
Supplier:  Avantor
DNase I
Catalog #: CA10029-182
Supplier:  Avantor
Discontinued
Item requires temperature control for storage and delivery with additional fees. It's not eligible for return due to safety and quality concerns. Consider requirements before purchasing.
Restricted Products: To process your orders without delay, please provide the required business documentation to purchase this product.

To order chemicals, medical devices, or other restricted products please provide ID that includes your business name & shipping address via email [email protected] or fax 484.881.5997 referencing your VWR account number. Acceptable forms of ID are:

  • • State issued document with your organization's Federal Tax ID Number
  • • State issued document with your organization's Resale Tax ID Number
  • • City or County issued Business License
  • • State Department of Health Services License
  • • Any other ID issued by the State that includes the business name & address

* ATTN: California Customers may require additional documentation as part of the CA Health & Safety Code. Products that fall under this regulation will be placed on a mandatory 21-day hold after documentation is received. VWR will not lift restrictions for residential shipping addresses.

Specifications

  • Storage conditions:
    –20 °C
  • Enzyme name:
    DNase I
  • Cat. no.:
    CA10029-182

Specifications

About this item

PerfeCTa® DNase I is a recombinant bovine DNase I preparation that is free of any contaminating RNases or proteases.

  • Free of contaminating Rnases or proteases
  • Simple and rapid solution
  • Reverse transcription, quantitative PCR amplification

The proprietary reaction buffer and stop buffer support a simple heat-skill step that permanently inactivates all trace levels of DNase activity

Provides a simple and rapid solution to eliminate residual genomic DNA from total RNA preparations for expression profiling by reverse transcription quantitative PCR amplification (RT-qPCR) as well as other molecular biology applications.

Complete inactivation of DNase is critical before subsequent cDNA synthesis. Residual, or renatured, DNase will degrade cDNA product and thereby alter apparent expression levels.

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