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snap cell 505 star  (New England Biolabs)


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    Structured Review

    New England Biolabs snap cell 505 star
    Snap Cell 505 Star, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 94/100, based on 70 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/snap cell 505 star/product/New England Biolabs
    Average 94 stars, based on 70 article reviews
    snap cell 505 star - by Bioz Stars, 2025-11
    94/100 stars

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    New England Biolabs snap cell505 star
    ( A ) A cartoon showing a cell-SLB assay for TIRF imaging of PD1:Shp2 association in Jurkat or human CD4 + T cells. ( B ) Left, representative TIRF images of the indicated mGFP-tagged PD1 variants (green) and anti-Shp2 (magenta) at the interface of a Jurkat cell and the SLB as depicted in A . Right, dot plots showing the anti-Shp2 F.I. normalized to PD1 F.I. (n = 40 cells). ( C ) Same as B , except that human CD4 + T cells expressing the indicated PD1 variants were imaged (n = 40 cells). ( D, E ) Same as A, B , except that DO11.10 cells were observed. ( F ) AA sequence alignment of hu PD1 ICD and mo PD1 ICD , with ITIM, PRS, PEQ/H, and ITSM highlighted. ( G ) Cartoon of a liposome reconstitution assay for measuring PD1 ICD :Shp2 tSH2 interaction. ( H ) Left, representative time courses of <t>SC505</t> (Shp2 tSH2 ) F.I. at increasing concentrations of hu PD1 ICD . Right, % SC505 quenching 30 min after ATP addition plotted against the [ hu PD1 ICD ] and [ mo PD1 ICD ] (n = 3 independent experiments). ( I ) Bar graphs summarizing apparent K d of Shp2 tSH2 interaction with indicated PD1 ICD variants determined via assays shown in G and H (n = 3 independent experiments). ( J ) Left, representative TIRF images showing Shp2 recruitment to microclusters of indicated PD1 variants in a Jurkat-SLB assays. Right, dot plots showing anti-Shp2 F.I. normalized to PD1 F.I. (n = 40 cells). Scale bars: 5 µm. Data are mean ± SD. **P < 0.01; ***P < 0.001; ns, not significant; student’s t-test.
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    https://www.bioz.com/result/snap cell505 star/product/New England Biolabs
    Average 94 stars, based on 1 article reviews
    snap cell505 star - by Bioz Stars, 2025-11
    94/100 stars
      Buy from Supplier

    Image Search Results


    ( A ) A cartoon showing a cell-SLB assay for TIRF imaging of PD1:Shp2 association in Jurkat or human CD4 + T cells. ( B ) Left, representative TIRF images of the indicated mGFP-tagged PD1 variants (green) and anti-Shp2 (magenta) at the interface of a Jurkat cell and the SLB as depicted in A . Right, dot plots showing the anti-Shp2 F.I. normalized to PD1 F.I. (n = 40 cells). ( C ) Same as B , except that human CD4 + T cells expressing the indicated PD1 variants were imaged (n = 40 cells). ( D, E ) Same as A, B , except that DO11.10 cells were observed. ( F ) AA sequence alignment of hu PD1 ICD and mo PD1 ICD , with ITIM, PRS, PEQ/H, and ITSM highlighted. ( G ) Cartoon of a liposome reconstitution assay for measuring PD1 ICD :Shp2 tSH2 interaction. ( H ) Left, representative time courses of SC505 (Shp2 tSH2 ) F.I. at increasing concentrations of hu PD1 ICD . Right, % SC505 quenching 30 min after ATP addition plotted against the [ hu PD1 ICD ] and [ mo PD1 ICD ] (n = 3 independent experiments). ( I ) Bar graphs summarizing apparent K d of Shp2 tSH2 interaction with indicated PD1 ICD variants determined via assays shown in G and H (n = 3 independent experiments). ( J ) Left, representative TIRF images showing Shp2 recruitment to microclusters of indicated PD1 variants in a Jurkat-SLB assays. Right, dot plots showing anti-Shp2 F.I. normalized to PD1 F.I. (n = 40 cells). Scale bars: 5 µm. Data are mean ± SD. **P < 0.01; ***P < 0.001; ns, not significant; student’s t-test.

    Journal: bioRxiv

    Article Title: Evolutionary fingerprint in rodent PD1 confers weakened activity and enhanced tumor immunity compared to human PD1

    doi: 10.1101/2024.09.21.614250

    Figure Lengend Snippet: ( A ) A cartoon showing a cell-SLB assay for TIRF imaging of PD1:Shp2 association in Jurkat or human CD4 + T cells. ( B ) Left, representative TIRF images of the indicated mGFP-tagged PD1 variants (green) and anti-Shp2 (magenta) at the interface of a Jurkat cell and the SLB as depicted in A . Right, dot plots showing the anti-Shp2 F.I. normalized to PD1 F.I. (n = 40 cells). ( C ) Same as B , except that human CD4 + T cells expressing the indicated PD1 variants were imaged (n = 40 cells). ( D, E ) Same as A, B , except that DO11.10 cells were observed. ( F ) AA sequence alignment of hu PD1 ICD and mo PD1 ICD , with ITIM, PRS, PEQ/H, and ITSM highlighted. ( G ) Cartoon of a liposome reconstitution assay for measuring PD1 ICD :Shp2 tSH2 interaction. ( H ) Left, representative time courses of SC505 (Shp2 tSH2 ) F.I. at increasing concentrations of hu PD1 ICD . Right, % SC505 quenching 30 min after ATP addition plotted against the [ hu PD1 ICD ] and [ mo PD1 ICD ] (n = 3 independent experiments). ( I ) Bar graphs summarizing apparent K d of Shp2 tSH2 interaction with indicated PD1 ICD variants determined via assays shown in G and H (n = 3 independent experiments). ( J ) Left, representative TIRF images showing Shp2 recruitment to microclusters of indicated PD1 variants in a Jurkat-SLB assays. Right, dot plots showing anti-Shp2 F.I. normalized to PD1 F.I. (n = 40 cells). Scale bars: 5 µm. Data are mean ± SD. **P < 0.01; ***P < 0.001; ns, not significant; student’s t-test.

    Article Snippet: Snap-Cell505 star (SC505: #S9103S) was purchased from NEB.

    Techniques: Imaging, Expressing, Sequencing, Reconstitution Assay