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5 Jan 2016 ... This file can be emailed to [email protected] along with your GenBank ... before moving onto a different page so that any data you enter is not lost. ... Use the drop down menu to indicate whether the tag is on the N- or C ...
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2nd generation lentiviral plasmids utilize the viral LTR promoter for gene ... they kill off any cells that have not incorporated the lentiviral genome and those cells ...
When designing the repair template, do not include the PAM sequence present ... Selecting a specific genetic manipulation can be a good way to narrow down ...
Background; Tetracycline Off; Tetracycline On; Experimental Tips; Tet Plasmids ... tetR will bind to tetracycline and not to the TRE, permitting transcription.
As a general rule, the restriction sites in the MCS are unique and not located elsewhere ... Gene Knock-down Plasmids - Used for reducing the expression of an ...
Plasmid pCCL-PGK-SPdCas9-BFP-EGFP from Dr. Yonglun Luo's lab contains the insert ... Total vector size (bp) 12791. Modifications to backbone. no. Vector type ... Genome-wide determination of on-target and off-target characteristics for ...
If you are searching for a commercially available backbone vector, Addgene is not ... contact [email protected] and we can update you with the plasmid status.
Track Order. Select order number or PO number to start search. Order Number; PO Number. Sign Up for Our Newsletter. Receive the latest news, hot plasmids, ...
If you have not yet logged into an Addgene account (or do not have access): Navigate to our website and select Track Order . ... Return to Addgene.org ... Order number; If your order is in our system, you will be brought to the Order Status Page.
28 Aug 2014 ... Return to Addgene.org ... Addgene has curated a comprehensive vector database that will help you find ... Bonus: The dyes also run at predicted sizes so you can estimate how far down the gel your bands have traveled based on the dye! ... I hope these tips demonstrate that plasmid verification is not just ...
This way, when you want to make more plasmid DNA, the plasmid will already be in your desired bacterial strain and you will not need to obtain more competent ...