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transfection lentivirus constructs  (Genechem)

 
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    Genechem transfection lentivirus constructs
    Transfection Lentivirus Constructs, supplied by Genechem, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/transfected+construct/pm41501140-237-0-6?v=Genechem
    Average 86 stars, based on 1 article reviews
    transfection lentivirus constructs - by Bioz Stars, 2026-08
    86/100 stars

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    ( A - D ) Pannexins were expressed in HEK293 cells and voltage clamp recordings were performed at –60 mV. Both the first round ( A and B ) and the second round ( C and D ) fractions are shown. Blue bars indicate application of each fraction. ( E ) Current densities from second-round fractions. The number of recordings from different cells for each experiment (biological replicates) is shown in parenthesis. Error bars represent SEM. ( F ) and ( G ) Whole-cell currents obtained with <t>vector-transfected</t> control cells. Application of fraction #12 from the first round and fraction #7 from the second round are shown. Figure 1—figure supplement 2—source data 1. Electrophysiology data used for .
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    Pfizer Inc transfected construct ( homo sapiens ) , human: dld-1 ung ko clone e7 + pcmv_cry2_mcherry_ung2_ dpip

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    Image Search Results


    ( A - D ) Pannexins were expressed in HEK293 cells and voltage clamp recordings were performed at –60 mV. Both the first round ( A and B ) and the second round ( C and D ) fractions are shown. Blue bars indicate application of each fraction. ( E ) Current densities from second-round fractions. The number of recordings from different cells for each experiment (biological replicates) is shown in parenthesis. Error bars represent SEM. ( F ) and ( G ) Whole-cell currents obtained with vector-transfected control cells. Application of fraction #12 from the first round and fraction #7 from the second round are shown. Figure 1—figure supplement 2—source data 1. Electrophysiology data used for .

    Journal: eLife

    Article Title: ATP-release pannexin channels are gated by lysophospholipids

    doi: 10.7554/eLife.107067

    Figure Lengend Snippet: ( A - D ) Pannexins were expressed in HEK293 cells and voltage clamp recordings were performed at –60 mV. Both the first round ( A and B ) and the second round ( C and D ) fractions are shown. Blue bars indicate application of each fraction. ( E ) Current densities from second-round fractions. The number of recordings from different cells for each experiment (biological replicates) is shown in parenthesis. Error bars represent SEM. ( F ) and ( G ) Whole-cell currents obtained with vector-transfected control cells. Application of fraction #12 from the first round and fraction #7 from the second round are shown. Figure 1—figure supplement 2—source data 1. Electrophysiology data used for .

    Article Snippet: Transfected construct ( Homo-sapiens ) , PANX1 - shRNA #2 , BROAD Institute Genetic Perturbation Platform , TRCN0000154636 , Lentiviral construct to transfect and express the shRNA.

    Techniques: Plasmid Preparation, Transfection, Control

    Journal: eLife

    Article Title: ATP-release pannexin channels are gated by lysophospholipids

    doi: 10.7554/eLife.107067

    Figure Lengend Snippet:

    Article Snippet: Transfected construct ( Homo-sapiens ) , PANX1 - shRNA #2 , BROAD Institute Genetic Perturbation Platform , TRCN0000154636 , Lentiviral construct to transfect and express the shRNA.

    Techniques: Recombinant, Synthesized, Expressing, Plasmid Preparation, Transfection, Construct, shRNA

    Journal: eLife

    Article Title: N6-methyladenosine in DNA promotes genome stability

    doi: 10.7554/eLife.101626

    Figure Lengend Snippet:

    Article Snippet: Transfected construct ( Homo sapiens ) , Human: DLD-1 UNG KO Clone E7 + pCMV_Cry2_mCherry_UNG2_ DPIP , This paper , This paper , Pfizer, Inc.

    Techniques: Transfection, Construct, Recombinant, Retroviral, Plasmid Preparation, Sequencing, Purification, MTS Assay, Saline, Cell Culture, Labeling, Mass Spectrometry, Blocking Assay, Electroporation, CRISPR, Gene Expression, TaqMan Assay, Multiplex sample analysis, Protease Inhibitor, Software, Genome Wide, Knock-Out, Immunofluorescence, Microscopy, Imaging, Western Blot