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mouse monoclonal anti rh1  (Developmental Studies Hybridoma Bank)


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    Developmental Studies Hybridoma Bank mouse monoclonal anti rh1
    Mouse Monoclonal Anti Rh1, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 94/100, based on 21 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+monoclonal+anti+rh1/anti-rhodopsin+1/pmc09681215-407-57-61
    Average 94 stars, based on 21 article reviews
    mouse monoclonal anti rh1 - by Bioz Stars, 2026-08
    94/100 stars

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    Electroretinogram recordings from 1-day old (A) and 7-day-old (B) wild-type controls w 1118 , left column in both panels and w, PIP82 1bpΔ mutants, right column in both panels. Two stimulus paradigms were used to evaluate the light response of the animals. In the top row of both panels (A, B) flies were stimulated with increasing intensities of light (from -5.0 log attenuation to -1.0 log attenuation) at 470 nm. In the second row of both panels, flies were stimulated with full intensity light at the wavelengths indicated. In both control and mutant animals, a prolonged-depolarizing afterpotential (PDA) is induced. Full intensity (unattenuated) light was 1.6 mW/cm 2 at 470 nm and 2.0 mW/cm 2 at 570 nm. C. Western analysis of <t>Rh1</t> levels as compared to Actin in w , PIP82 1bpΔ mutants and w 1118 controls.
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    Electroretinogram recordings from 1-day old (A) and 7-day-old (B) wild-type controls w 1118 , left column in both panels and w, PIP82 1bpΔ mutants, right column in both panels. Two stimulus paradigms were used to evaluate the light response of the animals. In the top row of both panels (A, B) flies were stimulated with increasing intensities of light (from -5.0 log attenuation to -1.0 log attenuation) at 470 nm. In the second row of both panels, flies were stimulated with full intensity light at the wavelengths indicated. In both control and mutant animals, a prolonged-depolarizing afterpotential (PDA) is induced. Full intensity (unattenuated) light was 1.6 mW/cm 2 at 470 nm and 2.0 mW/cm 2 at 570 nm. C. Western analysis of <t>Rh1</t> levels as compared to Actin in w , PIP82 1bpΔ mutants and w 1118 controls.
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    Electroretinogram recordings from 1-day old (A) and 7-day-old (B) wild-type controls w 1118 , left column in both panels and w, PIP82 1bpΔ mutants, right column in both panels. Two stimulus paradigms were used to evaluate the light response of the animals. In the top row of both panels (A, B) flies were stimulated with increasing intensities of light (from -5.0 log attenuation to -1.0 log attenuation) at 470 nm. In the second row of both panels, flies were stimulated with full intensity light at the wavelengths indicated. In both control and mutant animals, a prolonged-depolarizing afterpotential (PDA) is induced. Full intensity (unattenuated) light was 1.6 mW/cm 2 at 470 nm and 2.0 mW/cm 2 at 570 nm. C. Western analysis of Rh1 levels as compared to Actin in w , PIP82 1bpΔ mutants and w 1118 controls.

    Journal: PLoS Genetics

    Article Title: The brachyceran de novo gene PIP82, a phosphorylation target of aPKC, is essential for proper formation and maintenance of the rhabdomeric photoreceptor apical domain in Drosophila

    doi: 10.1371/journal.pgen.1008890

    Figure Lengend Snippet: Electroretinogram recordings from 1-day old (A) and 7-day-old (B) wild-type controls w 1118 , left column in both panels and w, PIP82 1bpΔ mutants, right column in both panels. Two stimulus paradigms were used to evaluate the light response of the animals. In the top row of both panels (A, B) flies were stimulated with increasing intensities of light (from -5.0 log attenuation to -1.0 log attenuation) at 470 nm. In the second row of both panels, flies were stimulated with full intensity light at the wavelengths indicated. In both control and mutant animals, a prolonged-depolarizing afterpotential (PDA) is induced. Full intensity (unattenuated) light was 1.6 mW/cm 2 at 470 nm and 2.0 mW/cm 2 at 570 nm. C. Western analysis of Rh1 levels as compared to Actin in w , PIP82 1bpΔ mutants and w 1118 controls.

    Article Snippet: The immuno-blot PVDF membrane (Bio-Rad) was incubated simultaneously with mouse monoclonal anti-Rh1 antibody (4C5, Developmental Studies Hybridoma Bank) and rabbit polyclonal anti-actin (Abcam ab1801) overnight at room temperature.

    Techniques: Control, Mutagenesis, Western Blot

    A-D. wild type, w 1118 , and E-H. w , PIP82 1bpΔ mutant photoreceptors stained for Rh1 (magenta) and MyoV (green) and F-Actin. The arrows highlight the distribution of Rh1 on the basal-lateral membrane. Each image is a single confocal section. All retinas are 1-day old and light exposed. Scale bar is 10uM.

    Journal: PLoS Genetics

    Article Title: The brachyceran de novo gene PIP82, a phosphorylation target of aPKC, is essential for proper formation and maintenance of the rhabdomeric photoreceptor apical domain in Drosophila

    doi: 10.1371/journal.pgen.1008890

    Figure Lengend Snippet: A-D. wild type, w 1118 , and E-H. w , PIP82 1bpΔ mutant photoreceptors stained for Rh1 (magenta) and MyoV (green) and F-Actin. The arrows highlight the distribution of Rh1 on the basal-lateral membrane. Each image is a single confocal section. All retinas are 1-day old and light exposed. Scale bar is 10uM.

    Article Snippet: The immuno-blot PVDF membrane (Bio-Rad) was incubated simultaneously with mouse monoclonal anti-Rh1 antibody (4C5, Developmental Studies Hybridoma Bank) and rabbit polyclonal anti-actin (Abcam ab1801) overnight at room temperature.

    Techniques: Mutagenesis, Staining, Membrane