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rabbit polyclonal anti rab9 antibody  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology rabbit polyclonal anti rab9 antibody
    Rabbit Polyclonal Anti Rab9 Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 39 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal anti rab9 antibody/product/Santa Cruz Biotechnology
    Average 92 stars, based on 39 article reviews
    rabbit polyclonal anti rab9 antibody - by Bioz Stars, 2026-06
    92/100 stars

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    Santa Cruz Biotechnology rab9 polyclonal antibody
    Subcellular distribution of type II collagen (CII) in macrophages. (a) Macrophages were subjected to subcellular fractionation and Percoll fractions were analyzed for the expression of the plasma membrane-associated enzyme alkaline phosphodiesterase I (open diamonds), the lysosomal enzyme β-hexosaminidase (closed diamonds) and markers of late endosomes Rab7 (closed circles) and <t>Rab9</t> (open circles); 27% Percoll alone is shown as fraction 0. Enzyme activity was measured as absorbance at 405 nm. Goat serum was used as a negative control (squares). (b) Macrophages were incubated in the absence (open circles) or presence of 200 μg/ml CII for 30 minutes and chased for 1 (open diamonds), 3 (closed diamonds), 5 (squares) and 24 h (closed circles) followed by subcellular fractionation and CII-specific ELISA. (c-d) Macrophages were pulse-chased with CII as above: (c) in the absence (closed squares) or presence of cytochalasin D (closed circles), amiloride (open squares) and 5-(N,N-dimethyl)amiloride (DMA; open circles); (d) in the presence of monodansylcadaverine (MDC; open diamonds) and filipin (closed diamonds) in the doses shown in the legend to Figure 1 or in the absence of CII and inhibitors (triangles). Cells were subjected to subcellular fractionation followed by CII-specific ELISA. Absorbance was measured at 405 nm. One of two experiments showing essentially the same results is shown. Error bars denote standard deviation.
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    Subcellular distribution of type II collagen (CII) in macrophages. (a) Macrophages were subjected to subcellular fractionation and Percoll fractions were analyzed for the expression of the plasma membrane-associated enzyme alkaline phosphodiesterase I (open diamonds), the lysosomal enzyme β-hexosaminidase (closed diamonds) and markers of late endosomes Rab7 (closed circles) and Rab9 (open circles); 27% Percoll alone is shown as fraction 0. Enzyme activity was measured as absorbance at 405 nm. Goat serum was used as a negative control (squares). (b) Macrophages were incubated in the absence (open circles) or presence of 200 μg/ml CII for 30 minutes and chased for 1 (open diamonds), 3 (closed diamonds), 5 (squares) and 24 h (closed circles) followed by subcellular fractionation and CII-specific ELISA. (c-d) Macrophages were pulse-chased with CII as above: (c) in the absence (closed squares) or presence of cytochalasin D (closed circles), amiloride (open squares) and 5-(N,N-dimethyl)amiloride (DMA; open circles); (d) in the presence of monodansylcadaverine (MDC; open diamonds) and filipin (closed diamonds) in the doses shown in the legend to Figure 1 or in the absence of CII and inhibitors (triangles). Cells were subjected to subcellular fractionation followed by CII-specific ELISA. Absorbance was measured at 405 nm. One of two experiments showing essentially the same results is shown. Error bars denote standard deviation.

    Journal: Arthritis Research & Therapy

    Article Title: Inhibition of macropinocytosis blocks antigen presentation of type II collagen in vitro and in vivo in HLA-DR1 transgenic mice

    doi: 10.1186/ar1964

    Figure Lengend Snippet: Subcellular distribution of type II collagen (CII) in macrophages. (a) Macrophages were subjected to subcellular fractionation and Percoll fractions were analyzed for the expression of the plasma membrane-associated enzyme alkaline phosphodiesterase I (open diamonds), the lysosomal enzyme β-hexosaminidase (closed diamonds) and markers of late endosomes Rab7 (closed circles) and Rab9 (open circles); 27% Percoll alone is shown as fraction 0. Enzyme activity was measured as absorbance at 405 nm. Goat serum was used as a negative control (squares). (b) Macrophages were incubated in the absence (open circles) or presence of 200 μg/ml CII for 30 minutes and chased for 1 (open diamonds), 3 (closed diamonds), 5 (squares) and 24 h (closed circles) followed by subcellular fractionation and CII-specific ELISA. (c-d) Macrophages were pulse-chased with CII as above: (c) in the absence (closed squares) or presence of cytochalasin D (closed circles), amiloride (open squares) and 5-(N,N-dimethyl)amiloride (DMA; open circles); (d) in the presence of monodansylcadaverine (MDC; open diamonds) and filipin (closed diamonds) in the doses shown in the legend to Figure 1 or in the absence of CII and inhibitors (triangles). Cells were subjected to subcellular fractionation followed by CII-specific ELISA. Absorbance was measured at 405 nm. One of two experiments showing essentially the same results is shown. Error bars denote standard deviation.

    Article Snippet: Plates were washed and incubated for 1 hour with goat anti-CII polyclonal antibody, goat anti-Rab7 and Rab9 polyclonal antibody (1: 200; Santa Cruz Biotechnology, Inc., Heidelberg, Germany).

    Techniques: Fractionation, Expressing, Clinical Proteomics, Membrane, Activity Assay, Negative Control, Incubation, Enzyme-linked Immunosorbent Assay, Standard Deviation