trpc1  (Alomone Labs)


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  • 94

    Structured Review

    Alomone Labs trpc1
    ( A ) Four clusters found in the dataset of force-distance (F-D) traces pulled from NG108-15 cells wild type. ( B ) The Bayesian identification of the clusters in ( A ) with the candidate membrane proteins. ( C ) Confocal images of NG108-15 cells overexpressing the construct N2b-Protein-GFP, as reported by the green fluorescence emitted by GFP. ( D ) From left to right, color density plots (blue indicating a colocalization among F-D traces of more than 80%) of the clusters superimposed to an F-D curve bearing the N2B signature (85 nm segment with a flat force below 10 pN) obtained in the sample overexpressing the candidate protein TMEM16F, <t>TRPC1,</t> TRPC5, and TRPC6, respectively. ( E ) Global histogram of L c of the clusters in A and the clusters with the N2B signature from cells transfected with the corresponding construct. ( F ) Position of the most likely rupture regions of the proteins according to ( E ) superimposed to the cartoon of the cryo electron microscopy (cryo-EM) structure available in the PDB.
    Trpc1, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/trpc1/product/Alomone Labs
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    trpc1 - by Bioz Stars, 2023-01
    94/100 stars

    Images

    1) Product Images from "Unfolding and identification of membrane proteins in situ"

    Article Title: Unfolding and identification of membrane proteins in situ

    Journal: eLife

    doi: 10.7554/eLife.77427

    ( A ) Four clusters found in the dataset of force-distance (F-D) traces pulled from NG108-15 cells wild type. ( B ) The Bayesian identification of the clusters in ( A ) with the candidate membrane proteins. ( C ) Confocal images of NG108-15 cells overexpressing the construct N2b-Protein-GFP, as reported by the green fluorescence emitted by GFP. ( D ) From left to right, color density plots (blue indicating a colocalization among F-D traces of more than 80%) of the clusters superimposed to an F-D curve bearing the N2B signature (85 nm segment with a flat force below 10 pN) obtained in the sample overexpressing the candidate protein TMEM16F, TRPC1, TRPC5, and TRPC6, respectively. ( E ) Global histogram of L c of the clusters in A and the clusters with the N2B signature from cells transfected with the corresponding construct. ( F ) Position of the most likely rupture regions of the proteins according to ( E ) superimposed to the cartoon of the cryo electron microscopy (cryo-EM) structure available in the PDB.
    Figure Legend Snippet: ( A ) Four clusters found in the dataset of force-distance (F-D) traces pulled from NG108-15 cells wild type. ( B ) The Bayesian identification of the clusters in ( A ) with the candidate membrane proteins. ( C ) Confocal images of NG108-15 cells overexpressing the construct N2b-Protein-GFP, as reported by the green fluorescence emitted by GFP. ( D ) From left to right, color density plots (blue indicating a colocalization among F-D traces of more than 80%) of the clusters superimposed to an F-D curve bearing the N2B signature (85 nm segment with a flat force below 10 pN) obtained in the sample overexpressing the candidate protein TMEM16F, TRPC1, TRPC5, and TRPC6, respectively. ( E ) Global histogram of L c of the clusters in A and the clusters with the N2B signature from cells transfected with the corresponding construct. ( F ) Position of the most likely rupture regions of the proteins according to ( E ) superimposed to the cartoon of the cryo electron microscopy (cryo-EM) structure available in the PDB.

    Techniques Used: Construct, Fluorescence, Transfection, Electron Microscopy, Cryo-EM Sample Prep


    Figure Legend Snippet:

    Techniques Used: Plasmid Preparation, Modification, Transfection, Construct, Sequencing, Labeling, Isolation, Recombinant, Software, Staining