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iphone model device  (apple inc)

 
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    apple inc iphone model device
    Iphone Model Device, supplied by apple inc, 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/product/disassembly/device+disassembling+iphone+models/us09218316-159-20-25
    Average 90 stars, based on 1 article reviews
    iphone model device - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Disassembly apparatus
    Article Snippet: Additionally, Apple, Inc. has disclosed a device for disassembling iPhone models that is capable of separating items as small as screws from other materials.

    Article Title: Remotely controlling a self-propelled device in a virtualized environment
    Article Snippet: In some implementations, the computing device 500 is a mobile device, such as a cellular telephony messaging device that (e.g., IPHONE model device manufactured by APPLE INC.) or tablet (e.g., IPAD model device manufactured by APPLE INC.) which executes one or more applications for controlling movement and other operations of a self-propelled device.



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    Image Search Results


    ( A ) Areas of FAs (dots) in anti-p-paxillin–stained parental (P) and Col6-KR 344SQ cells (n ≥ 50 per group). ( B ) Representative TIRF micrograph of mCherry-paxillin-transfected 344SQ cells to detect FAs (arrows), Original magnification, ×60. ( C ) Disassembly T 1/2 of FAs (dots) in Col6-KR 344SQ cells determined based on 60 minute time-lapse sequences. ( D ) Areas of FAs (dots) in anti-p-paxillin–stained parental or LH2-WA 344SQ cells (n ≥ 50 per group). ( E ) Disassembly T 1/2 of FAs (dots) in parental and LH2-WA 344SQ cells determined based on 60 minute time-lapse sequences. ( F ) Quantification of activated ITGβ1 per cell (dot) by immunocytochemical analysis with antiactivated ITGβ1 antibody. ( G ) WB analysis of phospho- and total FAK in parental and Col6-KR 344SQ cells. Densitometric values normalized based on total FAK are under gel. ( H ) IP/WB analysis of Col6a3/ITGα2. WB analysis to detect Col6a3 was carried out on anti-ITGα2–immunoprecipitated proteins isolated from parental or Col6-KR 344SQ cells. Relative densitometric values are under gels. Total cell lysates (input). ( I ) Schematic illustration of findings. P values were determined using 1-way ANOVA ( A , D , and F ) or Student’s 2-tailed t test ( C and E ). **** P < 0.0001.

    Journal: The Journal of Clinical Investigation

    Article Title: Lysyl hydroxylase 2 glucosylates collagen VI to drive lung cancer progression

    doi: 10.1172/JCI189197

    Figure Lengend Snippet: ( A ) Areas of FAs (dots) in anti-p-paxillin–stained parental (P) and Col6-KR 344SQ cells (n ≥ 50 per group). ( B ) Representative TIRF micrograph of mCherry-paxillin-transfected 344SQ cells to detect FAs (arrows), Original magnification, ×60. ( C ) Disassembly T 1/2 of FAs (dots) in Col6-KR 344SQ cells determined based on 60 minute time-lapse sequences. ( D ) Areas of FAs (dots) in anti-p-paxillin–stained parental or LH2-WA 344SQ cells (n ≥ 50 per group). ( E ) Disassembly T 1/2 of FAs (dots) in parental and LH2-WA 344SQ cells determined based on 60 minute time-lapse sequences. ( F ) Quantification of activated ITGβ1 per cell (dot) by immunocytochemical analysis with antiactivated ITGβ1 antibody. ( G ) WB analysis of phospho- and total FAK in parental and Col6-KR 344SQ cells. Densitometric values normalized based on total FAK are under gel. ( H ) IP/WB analysis of Col6a3/ITGα2. WB analysis to detect Col6a3 was carried out on anti-ITGα2–immunoprecipitated proteins isolated from parental or Col6-KR 344SQ cells. Relative densitometric values are under gels. Total cell lysates (input). ( I ) Schematic illustration of findings. P values were determined using 1-way ANOVA ( A , D , and F ) or Student’s 2-tailed t test ( C and E ). **** P < 0.0001.

    Article Snippet: Time-lapse videos were analyzed for FA disassembly assays in Imaris spots tracking module in Surpass mode.

    Techniques: Staining, Transfection, Immunoprecipitation, Isolation