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rab8 protein  (Tsang MD Inc)

 
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    Tsang MD Inc rab8 protein
    Rab8 Protein, supplied by Tsang MD 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/rab8+protein/rab8+protein/10__7554_slash_elife__81016-191-6-12
    Average 90 stars, based on 1 article reviews
    rab8 protein - by Bioz Stars, 2026-09
    90/100 stars

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    other:

    Article Title: GJA1 depletion causes ciliary defects by affecting Rab11 trafficking to the ciliary base
    Article Snippet: Previous studies have also shown that Rab8 interacts with CP110 and BBS4 (Tsang et al., 2008; Tsang and Dynlacht, 2013; Nachury et al., 2007).



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    Detergent-solubilized bovine ROS (3.5 pmol of PDE6) were incubated with PrBP/δ-Sepharose (2 mg of PrBP/δ per milliliter of resin), and proteins bound to the resin (Bnd) were separated from unbound proteins (UB) by centrifugation. As a control for nonspecific binding to the resin (NS), identical samples were incubated with a large excess of PrBP/δ. Equivalent amounts of the starting sample (ROS) were also loaded. After SDS-PAGE and transfer to polyvinylidene difluoride, blots were probed with primary antibodies to GRK1, PDE6, <t>Rab8,</t> transducin β-subunit, and arrestin.
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    rab8 protein  (STARR Life Sciences)
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    STARR Life Sciences rab8 protein
    Detergent-solubilized bovine ROS (3.5 pmol of PDE6) were incubated with PrBP/δ-Sepharose (2 mg of PrBP/δ per milliliter of resin), and proteins bound to the resin (Bnd) were separated from unbound proteins (UB) by centrifugation. As a control for nonspecific binding to the resin (NS), identical samples were incubated with a large excess of PrBP/δ. Equivalent amounts of the starting sample (ROS) were also loaded. After SDS-PAGE and transfer to polyvinylidene difluoride, blots were probed with primary antibodies to GRK1, PDE6, <t>Rab8,</t> transducin β-subunit, and arrestin.
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    Detergent-solubilized bovine ROS (3.5 pmol of PDE6) were incubated with PrBP/δ-Sepharose (2 mg of PrBP/δ per milliliter of resin), and proteins bound to the resin (Bnd) were separated from unbound proteins (UB) by centrifugation. As a control for nonspecific binding to the resin (NS), identical samples were incubated with a large excess of PrBP/δ. Equivalent amounts of the starting sample (ROS) were also loaded. After SDS-PAGE and transfer to polyvinylidene difluoride, blots were probed with primary antibodies to GRK1, PDE6, Rab8, transducin β-subunit, and arrestin.

    Journal: The Journal of Biological Chemistry

    Article Title: Evaluation of the 17-kDa Prenyl-binding Protein as a Regulatory Protein for Phototransduction in Retinal Photoreceptors *

    doi: 10.1074/jbc.M410475200

    Figure Lengend Snippet: Detergent-solubilized bovine ROS (3.5 pmol of PDE6) were incubated with PrBP/δ-Sepharose (2 mg of PrBP/δ per milliliter of resin), and proteins bound to the resin (Bnd) were separated from unbound proteins (UB) by centrifugation. As a control for nonspecific binding to the resin (NS), identical samples were incubated with a large excess of PrBP/δ. Equivalent amounts of the starting sample (ROS) were also loaded. After SDS-PAGE and transfer to polyvinylidene difluoride, blots were probed with primary antibodies to GRK1, PDE6, Rab8, transducin β-subunit, and arrestin.

    Article Snippet: Commercial antibodies to other proteins included the following: rod transducin α-subunit (K-20, Santa Cruz Biotechnology), rhodopsin (1D4, Chemicon) ( 25 ), opsin kinase (G-8, Affinity Bioreagents) ( 26 ), and Rab8 protein (Rab8, BD Biosciences).

    Techniques: Incubation, Centrifugation, Binding Assay, SDS Page