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human neuronal precursor cell line nt2  (Agilent technologies)


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    Structured Review

    Agilent technologies human neuronal precursor cell line nt2
    Acidification disables the safety catch and promotes procaspase-3 activation. (a) Ac-DEVD-AMC cleavage activity in procaspase-3 expressing bacterial extracts after incubation in buffers at varying pH levels. (b) α-Caspase-3 immunoblot and corresponding Ac-DEVD-AMC cleavage activity in cytosolic extracts from the neuronal precursor cells <t>NT2</t> treated as described in a.
    Human Neuronal Precursor Cell Line Nt2, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human neuronal precursor cell line nt2/product/Agilent technologies
    Average 90 stars, based on 1 article reviews
    human neuronal precursor cell line nt2 - by Bioz Stars, 2026-02
    90/100 stars

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    1) Product Images from "Maintenance of caspase-3 proenzyme dormancy by an intrinsic "safety catch" regulatory tripeptide"

    Article Title: Maintenance of caspase-3 proenzyme dormancy by an intrinsic "safety catch" regulatory tripeptide

    Journal:

    doi: 10.1073/pnas.111085198

    Acidification disables the safety catch and promotes procaspase-3 activation. (a) Ac-DEVD-AMC cleavage activity in procaspase-3 expressing bacterial extracts after incubation in buffers at varying pH levels. (b) α-Caspase-3 immunoblot and corresponding Ac-DEVD-AMC cleavage activity in cytosolic extracts from the neuronal precursor cells NT2 treated as described in a.
    Figure Legend Snippet: Acidification disables the safety catch and promotes procaspase-3 activation. (a) Ac-DEVD-AMC cleavage activity in procaspase-3 expressing bacterial extracts after incubation in buffers at varying pH levels. (b) α-Caspase-3 immunoblot and corresponding Ac-DEVD-AMC cleavage activity in cytosolic extracts from the neuronal precursor cells NT2 treated as described in a.

    Techniques Used: Activation Assay, Activity Assay, Expressing, Incubation, Western Blot



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    human neuronal precursor cell line nt2  (Agilent technologies)
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    Agilent technologies human neuronal precursor cell line nt2
    Acidification disables the safety catch and promotes procaspase-3 activation. (a) Ac-DEVD-AMC cleavage activity in procaspase-3 expressing bacterial extracts after incubation in buffers at varying pH levels. (b) α-Caspase-3 immunoblot and corresponding Ac-DEVD-AMC cleavage activity in cytosolic extracts from the neuronal precursor cells <t>NT2</t> treated as described in a.
    Human Neuronal Precursor Cell Line Nt2, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human neuronal precursor cell line nt2/product/Agilent technologies
    Average 90 stars, based on 1 article reviews
    human neuronal precursor cell line nt2 - by Bioz Stars, 2026-02
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Acidification disables the safety catch and promotes procaspase-3 activation. (a) Ac-DEVD-AMC cleavage activity in procaspase-3 expressing bacterial extracts after incubation in buffers at varying pH levels. (b) α-Caspase-3 immunoblot and corresponding Ac-DEVD-AMC cleavage activity in cytosolic extracts from the neuronal precursor cells NT2 treated as described in a.

    Journal:

    Article Title: Maintenance of caspase-3 proenzyme dormancy by an intrinsic "safety catch" regulatory tripeptide

    doi: 10.1073/pnas.111085198

    Figure Lengend Snippet: Acidification disables the safety catch and promotes procaspase-3 activation. (a) Ac-DEVD-AMC cleavage activity in procaspase-3 expressing bacterial extracts after incubation in buffers at varying pH levels. (b) α-Caspase-3 immunoblot and corresponding Ac-DEVD-AMC cleavage activity in cytosolic extracts from the neuronal precursor cells NT2 treated as described in a.

    Article Snippet: Lysates were prepared from the E. coli strain BL21(DE3) pLysS as described above or from the human neuronal precursor cell line NT2 (Stratagene) according to the procedure described ( 6 ).

    Techniques: Activation Assay, Activity Assay, Expressing, Incubation, Western Blot