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rpe 65  (Novus Biologicals)


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    Structured Review

    Novus Biologicals rpe 65
    Rpe 65, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 95/100, based on 45 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rpe+65/RPE65+Antibody+(401%2E8B11%2E3D9)+-+BSA+Free/pm39384746-140-37-41
    Average 95 stars, based on 45 article reviews
    rpe 65 - by Bioz Stars, 2026-10
    95/100 stars

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    Related Articles

    Incubation:

    Article Title: Equivalence of conventionally-derived and parthenote-derived human embryonic stem cells.
    Article Snippet: .. Following permeabilization with 0.1% Triton-X100/PBS for 40 min, the cells were rinsed with PBS and incubated overnight at 4uC in a humidified chamber with the primary antibody: ZO1 (1:50, Invitrogen), RPE-65 (1:250, Novus Biologicals), Bestrophin (1:25, Novus Biologicals), Occludin (1:50, Santa Cruz Biotechnology, Inc.) and CRALBP (1:50, Santa Cruz Biotechnology, Inc.). .. The cells were rinsed three times with PBS for 15 min and incubated at PLoS ONE | www.plosone.org 3 January 2011 | Volume 6 | Issue 1 | e14499 room temperature for 1 h with the secondary antibody: Alexa Fluor 546 donkey anti-mouse, Alexa Fluor 488 donkey antimouse, Alexa Fluor 546 donkey anti-rabbit or Alexa Fluor 488 donkey anti-goat (1:1000, Invitrogen).

    Article Title: Equivalence of Conventionally-Derived and Parthenote-Derived Human Embryonic Stem Cells
    Article Snippet: After electrophoresis, proteins were transferred to a Hybond-P polyvinylidene difluoride (PVDF) membrane (GE Healthcare Biosciences). .. Membranes were blocked for 2 hours in 5% nonfat milk in PBS-0.05% Tween-20 and incubated 2 hours in 5% nonfat milk containing primary antibodies: RPE-65 (1∶5000, Novus Biologicals), Bestrophin (1∶1000, Novus Biologicals) or NCAM1 (1∶2000, Santa Cruz Biotechnology, Inc.). .. Membranes were washed in PBS-0.05% Tween-20, then incubated for 1 hour at room temperature with secondary HRP-conjugated antibody goat anti-mouse (1∶1000, Millipore).

    Article Title: Regulation of T-lymphocyte CCL3 and CCL4 production by retinal pigment epithelial cells.
    Article Snippet: RESULTS.. Coculture of RPE cells with activated lymphocytes resulted in a reduction in CCL3 and CCL4 production by lymphocytes, primarily by soluble mediators.. Soluble CD54 was markedly increased on coculture of lymphocytes with RPE cells.

    Article Title: Equivalence of conventionally-derived and parthenote-derived human embryonic stem cells.
    Article Snippet: After electrophoresis, proteins were transferred to a Hybond-P polyvinylidene difluoride (PVDF) membrane (GE Healthcare Biosciences). .. Membranes were blocked for 2 hours in 5% nonfat milk in PBS-0.05% Tween-20 and incubated 2 hours in 5% nonfat milk containing primary antibodies: RPE-65 (1:5000, Novus Biologicals), Bestrophin (1:1000, Novus Biologicals) or NCAM1 (1:2000, Santa Cruz Biotechnology, Inc.). .. Membranes were washed in PBS-0.05% Tween-20, then incubated for 1 hour at room temperature with secondary HRP-conjugated antibody goat anti-mouse (1:1000, Millipore).

    Article Title: Equivalence of Conventionally-Derived and Parthenote-Derived Human Embryonic Stem Cells
    Article Snippet: .. Following permeabilization with 0.1% Triton-X100/PBS for 40 min, the cells were rinsed with PBS and incubated overnight at 4°C in a humidified chamber with the primary antibody: ZO1 (1∶50, Invitrogen), RPE-65 (1∶250, Novus Biologicals), Bestrophin (1∶25, Novus Biologicals), Occludin (1∶50, Santa Cruz Biotechnology, Inc.) and CRALBP (1∶50, Santa Cruz Biotechnology, Inc.). .. The cells were rinsed three times with PBS for 15 min and incubated at room temperature for 1 h with the secondary antibody: Alexa Fluor 546 donkey anti-mouse, Alexa Fluor 488 donkey anti-mouse, Alexa Fluor 546 donkey anti-rabbit or Alexa Fluor 488 donkey anti-goat (1∶1000, Invitrogen).

    Saline:

    Article Title: Regulation of T-lymphocyte CCL3 and CCL4 production by retinal pigment epithelial cells.
    Article Snippet: RESULTS.. Coculture of RPE cells with activated lymphocytes resulted in a reduction in CCL3 and CCL4 production by lymphocytes, primarily by soluble mediators.. Soluble CD54 was markedly increased on coculture of lymphocytes with RPE cells.

    Staining:

    Article Title: Regulation of T-lymphocyte CCL3 and CCL4 production by retinal pigment epithelial cells.
    Article Snippet: RESULTS.. Coculture of RPE cells with activated lymphocytes resulted in a reduction in CCL3 and CCL4 production by lymphocytes, primarily by soluble mediators.. Soluble CD54 was markedly increased on coculture of lymphocytes with RPE cells.

    Article Title: Annexin A2 promotes proliferative vitreoretinopathy in response to a macrophage inflammatory signal in mice.
    Article Snippet: .. In the Anxa2-/- eye, SMA is expressed in blood vessels; CD68-positive cells are rare. g, h Staining for SMA (red, rabbit anti-SMA, Cell Signaling 19245 T; 1:300 with donkey anti-rabbit Cy3, Jackson ImmunoResearch Laboratories 711-165-152; 1:300) and RPE-65 (green, mouse anti-RPE-65, Novus NB100-355; 1:150 with donkey anti-mouse Alexa 647, InvitrogenA31571; 1:100) inAnxa2+/+ (g) andAnxa2-/- (h) dispase-injected eyes. ..

    other:




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    Millipore anti-rpe-65 against rabbit rpe65 mab5428
    Histological and immunohistochemical analysis. ( a ) H&E staining image of control group without laser treatment showing the normal morphology of retinal cells and the architecture of retinal structure. All retinal tissues were clearly observed including ILM, GCL, IPL, INL, ONL, OPL, PL, RPE, choroid, and sclera. A single continuous RPE monolayer was detected. ( b ) H&E images without stem cells injection. RPE layers were significantly changed with discontinuities and regions of RPE loss were found in the RPE layer (yellow arrow). ( c ) H&E images of the tissues treated with laser followed by stem cell transplantation. Yellow arrows indicate the evidence of the transplanted hiPSC-RPE cells grafted in the subretinal space with high pigmentation (black color). ( d–o ) Immunofluorescent images of the tissues stained with two different antibodies: <t>RPE65</t> and NuMa. RPE65-positive indicate the signal from RPE cells. Red fluorescent color shows NuMa positive hiPSC-RPE cells. Blue fluorescent color demonstrates the cell’s nuclei stained by DAPI. No NuMa-positive signal was detected on the control group and laser treatment group. RPE loss was detected on treated group (yellow arrows). The hiPSC-RPE cells replaced RPE death were observed on the stem cell transplantation groups (Figure o ). Red arrows show the growing of hiPSC-RPE cells at the RPE damaged areas.
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    Image Search Results


    Histological and immunohistochemical analysis. ( a ) H&E staining image of control group without laser treatment showing the normal morphology of retinal cells and the architecture of retinal structure. All retinal tissues were clearly observed including ILM, GCL, IPL, INL, ONL, OPL, PL, RPE, choroid, and sclera. A single continuous RPE monolayer was detected. ( b ) H&E images without stem cells injection. RPE layers were significantly changed with discontinuities and regions of RPE loss were found in the RPE layer (yellow arrow). ( c ) H&E images of the tissues treated with laser followed by stem cell transplantation. Yellow arrows indicate the evidence of the transplanted hiPSC-RPE cells grafted in the subretinal space with high pigmentation (black color). ( d–o ) Immunofluorescent images of the tissues stained with two different antibodies: RPE65 and NuMa. RPE65-positive indicate the signal from RPE cells. Red fluorescent color shows NuMa positive hiPSC-RPE cells. Blue fluorescent color demonstrates the cell’s nuclei stained by DAPI. No NuMa-positive signal was detected on the control group and laser treatment group. RPE loss was detected on treated group (yellow arrows). The hiPSC-RPE cells replaced RPE death were observed on the stem cell transplantation groups (Figure o ). Red arrows show the growing of hiPSC-RPE cells at the RPE damaged areas.

    Journal: Scientific Reports

    Article Title: Selective nanosecond laser removal of retinal pigment epithelium for cell therapy

    doi: 10.1038/s41598-024-69917-z

    Figure Lengend Snippet: Histological and immunohistochemical analysis. ( a ) H&E staining image of control group without laser treatment showing the normal morphology of retinal cells and the architecture of retinal structure. All retinal tissues were clearly observed including ILM, GCL, IPL, INL, ONL, OPL, PL, RPE, choroid, and sclera. A single continuous RPE monolayer was detected. ( b ) H&E images without stem cells injection. RPE layers were significantly changed with discontinuities and regions of RPE loss were found in the RPE layer (yellow arrow). ( c ) H&E images of the tissues treated with laser followed by stem cell transplantation. Yellow arrows indicate the evidence of the transplanted hiPSC-RPE cells grafted in the subretinal space with high pigmentation (black color). ( d–o ) Immunofluorescent images of the tissues stained with two different antibodies: RPE65 and NuMa. RPE65-positive indicate the signal from RPE cells. Red fluorescent color shows NuMa positive hiPSC-RPE cells. Blue fluorescent color demonstrates the cell’s nuclei stained by DAPI. No NuMa-positive signal was detected on the control group and laser treatment group. RPE loss was detected on treated group (yellow arrows). The hiPSC-RPE cells replaced RPE death were observed on the stem cell transplantation groups (Figure o ). Red arrows show the growing of hiPSC-RPE cells at the RPE damaged areas.

    Article Snippet: To visualize the grafted hiPSC-RPE cells, IHC was performed using anti-RPE-65 against rabbit RPE65 (MAB5428, MilliporeSigma, MA, USA) and anti-NuMA antibodies against human NuMA (ab84680, Abcam, MA, USA).

    Techniques: Immunohistochemical staining, Staining, Control, Injection, Transplantation Assay