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#32996275   2020/10/23 To Up

A comparison of in vivo viral targeting systems identifies adeno-associated virus serotype 9 (AAV9) as an effective vector for genetic manipulation of Leydig cells in adult mice.

Despite the increasing popularity of deliverable transgenics, a robust and fully validated method for targeting Leydig cells, capable of delivering long-term transgene expression, is yet to be defined.
Annalucia Darbey, Diane Rebourcet, Michael Curley, Karen Kilcoyne, Nathan Jeffery, Natalie Reed, Laura Milne, Cornelia Roesl, Pamela Brown, Lee B Smith

2644 related Products with: A comparison of in vivo viral targeting systems identifies adeno-associated virus serotype 9 (AAV9) as an effective vector for genetic manipulation of Leydig cells in adult mice.

48 samples150ug200 100 2 ml100100 μg1 mL0.1ml1 mg96 assays

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