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rat anti tubulin primary antibody  (Bio-Rad)


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    Structured Review

    Bio-Rad rat anti tubulin primary antibody
    Rat Anti Tubulin Primary Antibody, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 938 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rat anti tubulin primary antibody/product/Bio-Rad
    Average 96 stars, based on 938 article reviews
    rat anti tubulin primary antibody - by Bioz Stars, 2026-06
    96/100 stars

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    Millipore rat α-tubulin primary antibody
    Spindle formation morphology in wild-type (WT, Col 0) and male sterile meiocytes. The spindle was detected by immunostaining <t>with</t> <t>anti-α-tubulin</t> antibody (green) and chromosomes were counterstained with DAPI (blue). Tubulin localization is similar in WT Col-0 and ams at prophase I (A, B), with normal spindle morphology during metaphase I in Col-0 (C) and ams (D). Radial microtubule arrays (RMA) however are disorganized in ams (F) compared with WT (E); this is also observed in the upstream male sterile mutants dyt1 (G) and tdf1 (H), but not the downstream mutant ms188 (I). Nucleus positioning within the tetrad is also unbalanced forming a ‘triad’ like shape in dyt1 , tdf1 , and ams (G–I). Scale bars: 5 μm.
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    Spindle formation morphology in wild-type (WT, Col 0) and male sterile meiocytes. The spindle was detected by immunostaining with anti-α-tubulin antibody (green) and chromosomes were counterstained with DAPI (blue). Tubulin localization is similar in WT Col-0 and ams at prophase I (A, B), with normal spindle morphology during metaphase I in Col-0 (C) and ams (D). Radial microtubule arrays (RMA) however are disorganized in ams (F) compared with WT (E); this is also observed in the upstream male sterile mutants dyt1 (G) and tdf1 (H), but not the downstream mutant ms188 (I). Nucleus positioning within the tetrad is also unbalanced forming a ‘triad’ like shape in dyt1 , tdf1 , and ams (G–I). Scale bars: 5 μm.

    Journal: Journal of Experimental Botany

    Article Title: Sporophytic control of pollen meiotic progression is mediated by tapetum expression of ABORTED MICROSPORES

    doi: 10.1093/jxb/erac225

    Figure Lengend Snippet: Spindle formation morphology in wild-type (WT, Col 0) and male sterile meiocytes. The spindle was detected by immunostaining with anti-α-tubulin antibody (green) and chromosomes were counterstained with DAPI (blue). Tubulin localization is similar in WT Col-0 and ams at prophase I (A, B), with normal spindle morphology during metaphase I in Col-0 (C) and ams (D). Radial microtubule arrays (RMA) however are disorganized in ams (F) compared with WT (E); this is also observed in the upstream male sterile mutants dyt1 (G) and tdf1 (H), but not the downstream mutant ms188 (I). Nucleus positioning within the tetrad is also unbalanced forming a ‘triad’ like shape in dyt1 , tdf1 , and ams (G–I). Scale bars: 5 μm.

    Article Snippet: After rinsing with potassium phosphate buffer, immobilized cells were then incubated overnight at room temperature with rat α-tubulin primary antibody (0.3%; clone B-5-1-2; Sigma-Aldrich) in phosphate-buffered saline (PBS) containing 0.1% Triton X-100 and 4.5 g l −1 BSA.

    Techniques: Sterility, Immunostaining, Mutagenesis