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rabbit anti mklp1 polyclonal antibody  (Novus Biologicals)


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    Novus Biologicals rabbit anti mklp1 polyclonal antibody
    Mos −/− eggs have defects in meiotic midbody formation. (A–D) Representative immunofluorescence images of wild-type (A) and Mos −/− eggs (B–D) showing localization of <t>MKLP1</t> (magenta), tubulin (green), and DNA (white). Arrowheads indicate structure features of MKLP1. Wild-type and Mos −/− oocytes were fixed 9–11.5 h after prophase I release. Scale bars: 10 µm. (E) Percentage of wild-type and Mos −/− eggs with normal or defective MKLP1 structure ( n indicates the number of eggs imaged per condition; three or more independent experiments conducted per condition). **** P <0.0001 (two-sided Fisher's exact test).
    Rabbit Anti Mklp1 Polyclonal Antibody, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+mklp1+antibodies/pmc13006522-280-5-9?v=Novus+Biologicals
    Average 94 stars, based on 10 article reviews
    rabbit anti mklp1 polyclonal antibody - by Bioz Stars, 2026-08
    94/100 stars

    Images

    1) Product Images from "MOS is a key regulator of meiotic midbody assembly and prevents abnormal divisions in mouse eggs and their polar bodies"

    Article Title: MOS is a key regulator of meiotic midbody assembly and prevents abnormal divisions in mouse eggs and their polar bodies

    Journal: Journal of Cell Science

    doi: 10.1242/jcs.264411

    Mos −/− eggs have defects in meiotic midbody formation. (A–D) Representative immunofluorescence images of wild-type (A) and Mos −/− eggs (B–D) showing localization of MKLP1 (magenta), tubulin (green), and DNA (white). Arrowheads indicate structure features of MKLP1. Wild-type and Mos −/− oocytes were fixed 9–11.5 h after prophase I release. Scale bars: 10 µm. (E) Percentage of wild-type and Mos −/− eggs with normal or defective MKLP1 structure ( n indicates the number of eggs imaged per condition; three or more independent experiments conducted per condition). **** P <0.0001 (two-sided Fisher's exact test).
    Figure Legend Snippet: Mos −/− eggs have defects in meiotic midbody formation. (A–D) Representative immunofluorescence images of wild-type (A) and Mos −/− eggs (B–D) showing localization of MKLP1 (magenta), tubulin (green), and DNA (white). Arrowheads indicate structure features of MKLP1. Wild-type and Mos −/− oocytes were fixed 9–11.5 h after prophase I release. Scale bars: 10 µm. (E) Percentage of wild-type and Mos −/− eggs with normal or defective MKLP1 structure ( n indicates the number of eggs imaged per condition; three or more independent experiments conducted per condition). **** P <0.0001 (two-sided Fisher's exact test).

    Techniques Used: Immunofluorescence



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    Mos −/− eggs have defects in meiotic midbody formation. (A–D) Representative immunofluorescence images of wild-type (A) and Mos −/− eggs (B–D) showing localization of <t>MKLP1</t> (magenta), tubulin (green), and DNA (white). Arrowheads indicate structure features of MKLP1. Wild-type and Mos −/− oocytes were fixed 9–11.5 h after prophase I release. Scale bars: 10 µm. (E) Percentage of wild-type and Mos −/− eggs with normal or defective MKLP1 structure ( n indicates the number of eggs imaged per condition; three or more independent experiments conducted per condition). **** P <0.0001 (two-sided Fisher's exact test).
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    Image Search Results


    Mos −/− eggs have defects in meiotic midbody formation. (A–D) Representative immunofluorescence images of wild-type (A) and Mos −/− eggs (B–D) showing localization of MKLP1 (magenta), tubulin (green), and DNA (white). Arrowheads indicate structure features of MKLP1. Wild-type and Mos −/− oocytes were fixed 9–11.5 h after prophase I release. Scale bars: 10 µm. (E) Percentage of wild-type and Mos −/− eggs with normal or defective MKLP1 structure ( n indicates the number of eggs imaged per condition; three or more independent experiments conducted per condition). **** P <0.0001 (two-sided Fisher's exact test).

    Journal: Journal of Cell Science

    Article Title: MOS is a key regulator of meiotic midbody assembly and prevents abnormal divisions in mouse eggs and their polar bodies

    doi: 10.1242/jcs.264411

    Figure Lengend Snippet: Mos −/− eggs have defects in meiotic midbody formation. (A–D) Representative immunofluorescence images of wild-type (A) and Mos −/− eggs (B–D) showing localization of MKLP1 (magenta), tubulin (green), and DNA (white). Arrowheads indicate structure features of MKLP1. Wild-type and Mos −/− oocytes were fixed 9–11.5 h after prophase I release. Scale bars: 10 µm. (E) Percentage of wild-type and Mos −/− eggs with normal or defective MKLP1 structure ( n indicates the number of eggs imaged per condition; three or more independent experiments conducted per condition). **** P <0.0001 (two-sided Fisher's exact test).

    Article Snippet: The primary antibodies used were: rabbit anti-MKLP1 polyclonal antibody (Novus NBP2-56923; 1:100) and rabbit anti-PRC1 polyclonal antibody (Proteintech 15617-1-AP; 1:100).

    Techniques: Immunofluorescence