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stereomicroscope lumar v.12  (Lumar Ideal II)

 
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    Lumar Ideal II stereomicroscope lumar v.12
    Stereomicroscope Lumar V.12, supplied by Lumar Ideal II, 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/stereomicroscope+lumar+v%2E12/stereomicroscope+lumar+v12/pm36869348-194-6-5
    Average 90 stars, based on 1 article reviews
    stereomicroscope lumar v.12 - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Injection:

    Article Title: The link between glycemic control measures and eye microvascular complications in a clinical cohort of type 2 diabetes with microRNA-223-3p signature.
    Article Snippet: Representative Images were captured using Lumar V.12 stereomicroscope and Nikon camera at ×25 (See figure on next page.) abnormality in the control group at 5% glucose and 10%, 50%, and 60% abnormality in the miR-223-3p mimic group at 0%, 2%, and 5% glucose, respectively (p = 0.02, p < 0.0001, and p < 0.05, respectively) (Fig. 4).

    Article Title: The link between glycemic control measures and eye microvascular complications in a clinical cohort of type 2 diabetes with microRNA-223-3p signature
    Article Snippet: Representative Images were captured using Lumar V.12 stereomicroscope and Nikon camera at ×25

    Article Title: Microinjection quality control in zebrafish model for genetic manipulations
    Article Snippet: Images were captured using Lumar V.12 stereomicroscope and Nikon camera at 40x objective.

    Article Title: Vaccinia Virus GLV-1h153 Is Effective in Treating and Preventing Metastatic Triple-Negative Breast Cancer
    Article Snippet: Objective: This study aimed to investigate the therapeutic impact of a new oncolytic vaccinia virus in a triple-negative breast cancer (TNBC) murine model and its potential for treating distant metastatic disease.. Background: TNBCs are aggressive tumors associated with a high metastatic rate.. Their lack of targets for hormonal/biological therapy presents significant clinical challenges and a dire need for novel therapies.

    Article Title: Microinjection quality control in zebrafish model for genetic manipulations
    Article Snippet: • Lumar V.12 stereomicroscope was used to screen fluorescent embryos using two channels (excitation 650 nm and emission 669 nm for m-cherry and 488nm and 509nm for e-GFP, respectively) at a different developmental interval time ( and ).

    Article Title: Microinjection quality control in zebrafish model for genetic manipulations
    Article Snippet: Representative images were captured at 80x objective using Lumar V.12 stereomicroscope.



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    Image Search Results


    Qualitative evaluation of natterin-like gene expression by whole-mount in situ Hybridization (WISH). Larvae after 24 h post-fertilization (hpf) were fixed, dehydrated, permeabilized and hybridized with the DIG-labeled probe, complementing the natterin-like RNA sequence (Qiagen, #339500 LCD0168623-BKG). Probe hybridization was determined by binding the AP-labeled anti-DIG antibody (#11093274910, Roche Diagnostics) and revealed through chromogenic reaction by NBT/BCIP solution. The images were obtained in the stereomicroscope STEREO LUMAR-V-12 Carl Zeiss. The picture snippets indicate the area of the larva’s body where the blue-purple precipitate (indicating gene product) can be observed in the non-depleted wild-type (WT) larvae (left), indicative of the presence of the natterin-like transcripts; and in the depleted (KO) larvae by CRISPR/Cas9 system (crRNA natterin-like WD07479944, Sigma) (right). The embryos body changed the shape due to long-lasting high temperature incubation in conical-bottom microtubes, not representing developmental malformations

    Journal: BMC Genomics

    Article Title: Natterin-like depletion by CRISPR/Cas9 impairs zebrafish ( Danio rerio ) embryonic development

    doi: 10.1186/s12864-022-08369-z

    Figure Lengend Snippet: Qualitative evaluation of natterin-like gene expression by whole-mount in situ Hybridization (WISH). Larvae after 24 h post-fertilization (hpf) were fixed, dehydrated, permeabilized and hybridized with the DIG-labeled probe, complementing the natterin-like RNA sequence (Qiagen, #339500 LCD0168623-BKG). Probe hybridization was determined by binding the AP-labeled anti-DIG antibody (#11093274910, Roche Diagnostics) and revealed through chromogenic reaction by NBT/BCIP solution. The images were obtained in the stereomicroscope STEREO LUMAR-V-12 Carl Zeiss. The picture snippets indicate the area of the larva’s body where the blue-purple precipitate (indicating gene product) can be observed in the non-depleted wild-type (WT) larvae (left), indicative of the presence of the natterin-like transcripts; and in the depleted (KO) larvae by CRISPR/Cas9 system (crRNA natterin-like WD07479944, Sigma) (right). The embryos body changed the shape due to long-lasting high temperature incubation in conical-bottom microtubes, not representing developmental malformations

    Article Snippet: The images were obtained in the stereomicroscope STEREO LUMAR-V-12 Carl Zeiss.

    Techniques: Expressing, In Situ Hybridization, Labeling, Sequencing, Hybridization, Binding Assay, CRISPR, Incubation