仔细阅读 发表于 2025-3-23 13:27:16

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侵略者 发表于 2025-3-23 14:24:16

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小口啜饮 发表于 2025-3-23 21:37:48

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resilience 发表于 2025-3-24 01:07:29

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ARCH 发表于 2025-3-24 02:39:25

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深陷 发表于 2025-3-24 08:25:51

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fidelity 发表于 2025-3-24 12:56:04

Measuring T Cell-to-T Cell HIV-1 Transfer, Viral Fusion, and Infection Using Flow Cytometryd an uninfected, CD4-expressing “target” cell. In vitro studies indicate that HIV-1 cell-to-cell infection is much more efficient than infection by cell-free viral particles; however, the exact mechanisms of the enhanced efficiency of this infection pathway are still unclear. Several assays have bee

江湖骗子 发表于 2025-3-24 18:07:18

HIV-1 Capsid Stabilization Assayfects in HIV-1 reverse transcription and infection. We developed a novel and simple assay to measure stability of in vitro-assembled HIV-1 CA-NC complexes. This assay allowed us to demonstrate that cytosolic extracts strongly stabilize the HIV-1 core (Fricke et al., J Virol 87:10587–10597, 2013). By

原告 发表于 2025-3-24 20:12:32

Detection and Tracking of Dual-Labeled HIV Particles Using Wide-Field Live Cell Imaging to Follow Vi of production and imaging of dual-labeled HIV viral particles that allows the visualization of two events. Varying release of the intravirion fluid phase marker reveals virion fusion and the loss of the integrity of HIV viral cores with the use of live wide-field fluorescent microscopy.

antipsychotic 发表于 2025-3-25 03:10:01

HIV-1 Reverse Transcriptase-Based Assay to Determine Cellular dNTP Concentrations methods are currently employed to determine dNTP concentrations from cellular extracts. Here, we describe a highly efficient, HIV-1 reverse transcriptase (RT)-based assay to quantitate dNTP concentrations. The assay is based on the ability of HIV-1 RT to function at very low dNTP concentrations, th
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查看完整版本: Titlebook: HIV Protocols; Vinayaka R. Prasad,Ganjam V. Kalpana Book 2016Latest edition Springer Science+Business Media New York 2016 HIV-1 RNA struct