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rabbit anti human rab7  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc rabbit anti human rab7
    Rabbit Anti Human Rab7, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 311 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit anti human rab7/product/Cell Signaling Technology Inc
    Average 96 stars, based on 311 article reviews
    rabbit anti human rab7 - by Bioz Stars, 2026-06
    96/100 stars

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    Santa Cruz Biotechnology rabbit anti human rab7
    CRISPR LNPs Cell Trafficking. Rhodamine conjugated DHPE (1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine) phosphoglycerol tracked the locale of CRISPR LNPs in human MDMs. Confocal microscopy was employed 12 h after LNPs injection in the MDM cultures. Alexa-Fluor 488 (green) secondary antibody detected Rab 5, <t>Rab7,</t> or Lamp1 subcellular compartments. Phalloidin-iFluor 647 marked cell boundaries. The MDM nucleus was stained with DAPI (blue). Rhodamine DHPE phospholipid containing CRISPR-LNPs (red) colocalized with Rab5 (a) and Rab7 (green) (b). (c) No colocalization was found between Lamp1 (green) and the nanoparticles (red). (d) TM-Rhodamine labeled px333DE was used for CRISPR LNPs to examine nuclear localization of the CRISPR payload present in the nucleus 12h after treatment. Z-stack affirmed that the CRISPR reached the nucleus.
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    Cell Signaling Technology Inc anti human rab7
    Huh7-NTCP cells were grown on glass cover slides and fixed 48 hr after seeding. ( A ) Endogenous ERp57 with Rab5, <t>Rab7,</t> Rab11, or Lamp1 were immune-stained, and the colocalization of ERp57 (red channels) with Rab5, Rab7, Rab11, or Lamp1 (green channels) was analyzed by confocal microscopy. Scale bars of panels and zooms from squared area represent 10 µm and 2 µm, respectively. ( B ) The degree of colocalization between ERp57 and the different cell markers was assessed by determining the Pearson’s correlation coefficients with the JACoP plugin of ImageJ. Results are expressed as the mean of six individual cells. Error bars correspond to standard deviations.
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    Image Search Results


    CRISPR LNPs Cell Trafficking. Rhodamine conjugated DHPE (1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine) phosphoglycerol tracked the locale of CRISPR LNPs in human MDMs. Confocal microscopy was employed 12 h after LNPs injection in the MDM cultures. Alexa-Fluor 488 (green) secondary antibody detected Rab 5, Rab7, or Lamp1 subcellular compartments. Phalloidin-iFluor 647 marked cell boundaries. The MDM nucleus was stained with DAPI (blue). Rhodamine DHPE phospholipid containing CRISPR-LNPs (red) colocalized with Rab5 (a) and Rab7 (green) (b). (c) No colocalization was found between Lamp1 (green) and the nanoparticles (red). (d) TM-Rhodamine labeled px333DE was used for CRISPR LNPs to examine nuclear localization of the CRISPR payload present in the nucleus 12h after treatment. Z-stack affirmed that the CRISPR reached the nucleus.

    Journal: EBioMedicine

    Article Title: CRISPR-Cas9 Mediated Exonic Disruption for HIV-1 Elimination

    doi: 10.1016/j.ebiom.2021.103678

    Figure Lengend Snippet: CRISPR LNPs Cell Trafficking. Rhodamine conjugated DHPE (1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine) phosphoglycerol tracked the locale of CRISPR LNPs in human MDMs. Confocal microscopy was employed 12 h after LNPs injection in the MDM cultures. Alexa-Fluor 488 (green) secondary antibody detected Rab 5, Rab7, or Lamp1 subcellular compartments. Phalloidin-iFluor 647 marked cell boundaries. The MDM nucleus was stained with DAPI (blue). Rhodamine DHPE phospholipid containing CRISPR-LNPs (red) colocalized with Rab5 (a) and Rab7 (green) (b). (c) No colocalization was found between Lamp1 (green) and the nanoparticles (red). (d) TM-Rhodamine labeled px333DE was used for CRISPR LNPs to examine nuclear localization of the CRISPR payload present in the nucleus 12h after treatment. Z-stack affirmed that the CRISPR reached the nucleus.

    Article Snippet: The following primary antibodies were used to label different endosomal compartments: Rabbit anti-human Rab5, (Abcam #ab18211), early endosomal marker, rabbit anti-human Rab7 (Santacruz biotechnology #sc10767), a late endosome marker, and rabbit anti-human Lamp-1 (lysosomal-associated membrane protein-1) (Abcam #ab24170) for lysosomes.

    Techniques: CRISPR, Confocal Microscopy, Injection, Staining, Labeling

    Huh7-NTCP cells were grown on glass cover slides and fixed 48 hr after seeding. ( A ) Endogenous ERp57 with Rab5, Rab7, Rab11, or Lamp1 were immune-stained, and the colocalization of ERp57 (red channels) with Rab5, Rab7, Rab11, or Lamp1 (green channels) was analyzed by confocal microscopy. Scale bars of panels and zooms from squared area represent 10 µm and 2 µm, respectively. ( B ) The degree of colocalization between ERp57 and the different cell markers was assessed by determining the Pearson’s correlation coefficients with the JACoP plugin of ImageJ. Results are expressed as the mean of six individual cells. Error bars correspond to standard deviations.

    Journal: eLife

    Article Title: A fusion peptide in preS1 and the human protein disulfide isomerase ERp57 are involved in hepatitis B virus membrane fusion process

    doi: 10.7554/eLife.64507

    Figure Lengend Snippet: Huh7-NTCP cells were grown on glass cover slides and fixed 48 hr after seeding. ( A ) Endogenous ERp57 with Rab5, Rab7, Rab11, or Lamp1 were immune-stained, and the colocalization of ERp57 (red channels) with Rab5, Rab7, Rab11, or Lamp1 (green channels) was analyzed by confocal microscopy. Scale bars of panels and zooms from squared area represent 10 µm and 2 µm, respectively. ( B ) The degree of colocalization between ERp57 and the different cell markers was assessed by determining the Pearson’s correlation coefficients with the JACoP plugin of ImageJ. Results are expressed as the mean of six individual cells. Error bars correspond to standard deviations.

    Article Snippet: Antibody , Anti-human Rab7 (rabbit monoclonal) , Cell Signaling Technology , (D95F2):9367 , IF (1:100).

    Techniques: Staining, Confocal Microscopy

    Journal: eLife

    Article Title: A fusion peptide in preS1 and the human protein disulfide isomerase ERp57 are involved in hepatitis B virus membrane fusion process

    doi: 10.7554/eLife.64507

    Figure Lengend Snippet:

    Article Snippet: Antibody , Anti-human Rab7 (rabbit monoclonal) , Cell Signaling Technology , (D95F2):9367 , IF (1:100).

    Techniques: Virus, Produced, Variant Assay, Construct, Generated, Transduction, Retroviral, Plasmid Preparation, Selection, shRNA, Transfection, Expressing, Clone Assay, Luciferase, Isolation, Sequencing, Mutagenesis, Reporter Assay, Activity Assay, cDNA Synthesis, SYBR Green Assay, Membrane, Integrity Assay, Cytotoxicity Assay, Software, Staining, RNA Extraction