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Q:

Can I use EFS encrypted external drives with Drive Encryption enabled on my Windows 8 laptops?

I have two Windows 8 laptops that I am currently using to encrypt volumes on external drives using on-disk encryption. I have been looking at online information about the encryption and as far as I can tell I don’t need anything special to be able to access the EFS encrypted volumes. However, when looking at the Windows Easy Transfer app it says that the data on the drive is encrypted and therefore it cannot be moved. I thought that perhaps this might be due to having EFS (Encrypted File System) enabled on the external hard drive.
Is it possible to transfer files to and from EFS encrypted drives and will Drive Encryption (recommended for the backup usage) interfere with this?

A:

Drive Encryption by itself doesn’t do much with volumes you already encrypted.

When you configure BitLocker, the system creates a master key (MSK) that is used to encrypt and decrypt the entire volume.
When you encrypt or decrypt the volume, the volume’s AES key is derived from the MSK, and the new volume is fully encrypted or decrypted by decrypting the new volume.

This answer confirms the same:

First off, Windows 8 does not support EFS encryption without BitLocker enabled. This is mentioned in the end of this article. The second question is, whether or not EFS encryption without BitLocker configured, requires a new key to be generated, or if existing keys from previous encryption will work.

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We have previously reported that transfection of HeLa cells with the Bacillus thuringiensis-coded toxin CryIA(c) could prime MHC class II-restricted T-cell responses, and that this priming required the participation of a mouse gut symbiont. The present experiments evaluated whether transfection with CryIA(c) could prime CD4+ T-cells secreting interleukin 2 (IL-2) and specific for Bacillus thuringiensis-derived antigen. A transfected T-cell clone, CL14, specific for the CryIA(c) protein, expressed mRNAs for IL-2, interferon gamma, and tumor necrosis factor alpha. The frequency of spontaneously secreting cytokine-producing CL14 cells was increased by transfection with the toxin, and
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