jbscreen classic  (Jena Bioscience)


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    Jena Bioscience jbscreen classic
    Jbscreen Classic, supplied by Jena Bioscience, used in various techniques. Bioz Stars score: 85/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 85 stars, based on 7 article reviews
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    jbscreen classic - by Bioz Stars, 2022-09
    85/100 stars

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    Jena Bioscience cy3
    Incorporation on the BCN non-canonical amino acid into membrane proteins and labeling with a tetrazine-linked <t>Cy3</t> fluorophore derivative for the details on the purification of PglC and PglA variants in SMALP. (B) Quantitative evaluation of the efficiency of labeling in PglC. Data are represented as mean ± SEM, n = 3; replicates were performed on distinct CEF aliquots. .
    Cy3, supplied by Jena Bioscience, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    88
    Jena Bioscience fluorochrome atto647
    FISH mapping of clone 395 ( yellow ) to F. pratensis and L. perenne chromosomes. a Diploid (2n = 14) F. pratensis . b Tetraploid (2n = 28) F. pratensis . c Diploid (2n = 14) L. perenne . d Tetraploid (2n = 28) L. perenne . The clone was labeled with <t>Atto647</t> fluorochrome; chromosomes were counterstained with DAPI ( blue )
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    90
    Jena Bioscience mouse monoclonal anti octopamine antibody
    Sucrose feeding-evoked reporter protein expression in the DUM neurons of the IEG reporter line. A , Dorsal view of the subesophageal ganglion of the Hokudai WT strain stained with anti- Gryllus Tdc2 antibody. The outline of the ganglion is surrounded by the white dotted line. The depth of the cells is color coded as indicated in the inset. Rostrocaudal (R-C) axis was indicated. Scale bar represents 200 µm. See Fig. 7-1 for the <t>octopamine</t> biosynthesis pathway and the structures of the Tdc proteins in insects. See Fig. 7-2 for the frontal view of the supraesophageal ganglion and the ventral view of the subesophageal ganglion stained with anti- Gryllus Tdc2 antibody. B , Schematic drawing of the positions and numbers of the cell bodies of three DUM clusters (DUM1, DUM2, DUM3) on the dorsal side of the subesophageal ganglion. C , Double fluorescent immunostaining confirmed that the DUM neurons contain octopamine. The DUM neurons were stained with the anti- Gryllus Tdc2 antibody (green) and anti-octopamine antibody (magenta). Scale bar represents 50 µm. D , Distribution of the reporter protein (EYFPnls:PEST) in the DUM neurons of the IEG reporter line before and 6 h after feeding of sucrose solution ( n = 4 each). The DUM neurons were stained with the anti- Gryllus Tdc2 antibody (green) and anti-GFP antibody (magenta). The cell bodies of Gryllus Tdc2 immunoreactive DUM neurons are surrounded by the white dotted line. The DUM neurons with nuclear EYFP immunoreactivity are indicated by white arrowheads. Scale bar represents 50 µm.
    Mouse Monoclonal Anti Octopamine Antibody, supplied by Jena Bioscience, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    88
    Jena Bioscience l tarentolae
    Aminoglycoside effects on Leishmania and the leishmanial translation machinery. a Chemical structures of AGs used in the study. Ring numbers are indicated in red; the common 2-deoxystreptamine ring (ring II) is highlighted in yellow and the substitution patterns in derivatized compounds are given as R 1 and R 2 . b In vitro inhibition of cytosolic ribosome translation in L. <t>tarentolae</t> lysates. Each value represents the mean ± standard error of at least three independent experiments performed in duplicates. Hygromycin B (HYG, orange), Geneticin (G418, blue), Paromomycin (PAR, green), Gentamicin (GEN, pink), Neomycin (NEO, yellow), and Apramycin (APR, purple). c Inhibition of L. donovani promastigote growth by AGs. Values indicate drug concentrations inducing 50% inhibition of parasite growth (LC 50 ). Each value represents the mean ± standard error of at least three independent experiments performed in triplicates
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    Incorporation on the BCN non-canonical amino acid into membrane proteins and labeling with a tetrazine-linked Cy3 fluorophore derivative for the details on the purification of PglC and PglA variants in SMALP. (B) Quantitative evaluation of the efficiency of labeling in PglC. Data are represented as mean ± SEM, n = 3; replicates were performed on distinct CEF aliquots. .

    Journal: Cell chemical biology

    Article Title: A Strategic Approach for Fluorescence Imaging of Membrane Proteins in a Native-Like Environment

    doi: 10.1016/j.chembiol.2019.11.008

    Figure Lengend Snippet: Incorporation on the BCN non-canonical amino acid into membrane proteins and labeling with a tetrazine-linked Cy3 fluorophore derivative for the details on the purification of PglC and PglA variants in SMALP. (B) Quantitative evaluation of the efficiency of labeling in PglC. Data are represented as mean ± SEM, n = 3; replicates were performed on distinct CEF aliquots. .

    Article Snippet: Labeling membrane proteins in SMALP 100 μL of the eluted volume was mixed together with Cy3- or Cy5-tetrazine (1-10 μM, Jena Bioscience).

    Techniques: Labeling, Purification

    FISH mapping of clone 395 ( yellow ) to F. pratensis and L. perenne chromosomes. a Diploid (2n = 14) F. pratensis . b Tetraploid (2n = 28) F. pratensis . c Diploid (2n = 14) L. perenne . d Tetraploid (2n = 28) L. perenne . The clone was labeled with Atto647 fluorochrome; chromosomes were counterstained with DAPI ( blue )

    Journal: Protoplasma

    Article Title: Karyotype reshufflings of Festuca pratensis × Lolium perenne hybrids

    doi: 10.1007/s00709-017-1161-5

    Figure Lengend Snippet: FISH mapping of clone 395 ( yellow ) to F. pratensis and L. perenne chromosomes. a Diploid (2n = 14) F. pratensis . b Tetraploid (2n = 28) F. pratensis . c Diploid (2n = 14) L. perenne . d Tetraploid (2n = 28) L. perenne . The clone was labeled with Atto647 fluorochrome; chromosomes were counterstained with DAPI ( blue )

    Article Snippet: Probes Clone 395, derived from the library representing the most frequently present sequences in the F. pratensis genome, was labeled by nick translation with fluorochrome Atto647 (Jena BioScience) (Majka et al. ).

    Techniques: Fluorescence In Situ Hybridization, Labeling

    Sucrose feeding-evoked reporter protein expression in the DUM neurons of the IEG reporter line. A , Dorsal view of the subesophageal ganglion of the Hokudai WT strain stained with anti- Gryllus Tdc2 antibody. The outline of the ganglion is surrounded by the white dotted line. The depth of the cells is color coded as indicated in the inset. Rostrocaudal (R-C) axis was indicated. Scale bar represents 200 µm. See Fig. 7-1 for the octopamine biosynthesis pathway and the structures of the Tdc proteins in insects. See Fig. 7-2 for the frontal view of the supraesophageal ganglion and the ventral view of the subesophageal ganglion stained with anti- Gryllus Tdc2 antibody. B , Schematic drawing of the positions and numbers of the cell bodies of three DUM clusters (DUM1, DUM2, DUM3) on the dorsal side of the subesophageal ganglion. C , Double fluorescent immunostaining confirmed that the DUM neurons contain octopamine. The DUM neurons were stained with the anti- Gryllus Tdc2 antibody (green) and anti-octopamine antibody (magenta). Scale bar represents 50 µm. D , Distribution of the reporter protein (EYFPnls:PEST) in the DUM neurons of the IEG reporter line before and 6 h after feeding of sucrose solution ( n = 4 each). The DUM neurons were stained with the anti- Gryllus Tdc2 antibody (green) and anti-GFP antibody (magenta). The cell bodies of Gryllus Tdc2 immunoreactive DUM neurons are surrounded by the white dotted line. The DUM neurons with nuclear EYFP immunoreactivity are indicated by white arrowheads. Scale bar represents 50 µm.

    Journal: eNeuro

    Article Title: Immediate-Early Promoter-Driven Transgenic Reporter System for Neuroethological Research in a Hemimetabolous Insect

    doi: 10.1523/ENEURO.0061-18.2018

    Figure Lengend Snippet: Sucrose feeding-evoked reporter protein expression in the DUM neurons of the IEG reporter line. A , Dorsal view of the subesophageal ganglion of the Hokudai WT strain stained with anti- Gryllus Tdc2 antibody. The outline of the ganglion is surrounded by the white dotted line. The depth of the cells is color coded as indicated in the inset. Rostrocaudal (R-C) axis was indicated. Scale bar represents 200 µm. See Fig. 7-1 for the octopamine biosynthesis pathway and the structures of the Tdc proteins in insects. See Fig. 7-2 for the frontal view of the supraesophageal ganglion and the ventral view of the subesophageal ganglion stained with anti- Gryllus Tdc2 antibody. B , Schematic drawing of the positions and numbers of the cell bodies of three DUM clusters (DUM1, DUM2, DUM3) on the dorsal side of the subesophageal ganglion. C , Double fluorescent immunostaining confirmed that the DUM neurons contain octopamine. The DUM neurons were stained with the anti- Gryllus Tdc2 antibody (green) and anti-octopamine antibody (magenta). Scale bar represents 50 µm. D , Distribution of the reporter protein (EYFPnls:PEST) in the DUM neurons of the IEG reporter line before and 6 h after feeding of sucrose solution ( n = 4 each). The DUM neurons were stained with the anti- Gryllus Tdc2 antibody (green) and anti-GFP antibody (magenta). The cell bodies of Gryllus Tdc2 immunoreactive DUM neurons are surrounded by the white dotted line. The DUM neurons with nuclear EYFP immunoreactivity are indicated by white arrowheads. Scale bar represents 50 µm.

    Article Snippet: The DUM neurons were labeled with the guinea pig anti-Gryllus Tdc2 antibody (1:1000) and/or the mouse monoclonal anti-octopamine antibody (1:1000; Jena Bioscience, Cat# ABD-029, RRID: AB_2315000 ).

    Techniques: Expressing, Staining, Immunostaining

    Aminoglycoside effects on Leishmania and the leishmanial translation machinery. a Chemical structures of AGs used in the study. Ring numbers are indicated in red; the common 2-deoxystreptamine ring (ring II) is highlighted in yellow and the substitution patterns in derivatized compounds are given as R 1 and R 2 . b In vitro inhibition of cytosolic ribosome translation in L. tarentolae lysates. Each value represents the mean ± standard error of at least three independent experiments performed in duplicates. Hygromycin B (HYG, orange), Geneticin (G418, blue), Paromomycin (PAR, green), Gentamicin (GEN, pink), Neomycin (NEO, yellow), and Apramycin (APR, purple). c Inhibition of L. donovani promastigote growth by AGs. Values indicate drug concentrations inducing 50% inhibition of parasite growth (LC 50 ). Each value represents the mean ± standard error of at least three independent experiments performed in triplicates

    Journal: Nature Communications

    Article Title: Atomic resolution snapshot of Leishmania ribosome inhibition by the aminoglycoside paromomycin

    doi: 10.1038/s41467-017-01664-4

    Figure Lengend Snippet: Aminoglycoside effects on Leishmania and the leishmanial translation machinery. a Chemical structures of AGs used in the study. Ring numbers are indicated in red; the common 2-deoxystreptamine ring (ring II) is highlighted in yellow and the substitution patterns in derivatized compounds are given as R 1 and R 2 . b In vitro inhibition of cytosolic ribosome translation in L. tarentolae lysates. Each value represents the mean ± standard error of at least three independent experiments performed in duplicates. Hygromycin B (HYG, orange), Geneticin (G418, blue), Paromomycin (PAR, green), Gentamicin (GEN, pink), Neomycin (NEO, yellow), and Apramycin (APR, purple). c Inhibition of L. donovani promastigote growth by AGs. Values indicate drug concentrations inducing 50% inhibition of parasite growth (LC 50 ). Each value represents the mean ± standard error of at least three independent experiments performed in triplicates

    Article Snippet: L. tarentolae is a non-pathogenic Leishmania strain that does not cause disease in human.

    Techniques: In Vitro, Inhibition