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nanoparticle tracker particle metrix pmx 120 zetaview mono 488 laser  (Particle Metrix)

 
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    Particle Metrix nanoparticle tracker particle metrix pmx 120 zetaview mono 488 laser
    40,000 × g is sufficient to pellet the majority of plant EVs. Immunoblots, <t>nanoparticle</t> tracking analysis (NTA), and representative transmission electron microscopy (TEM) images of the indicated extracellular fractions from Arabidopsis rosettes processed by differential ultracentrifugation, as indicated in the diagram. For immunoblots, samples are apoplastic wash fluid (AWF) and the indicated pellets collected from 5 mL of AWF. Numbers on the left sides of immunoblots indicate sizes in kiloDaltons. The TET8 antibody strongly cross‐reacts with a <25 kDa protein abundant in EV pellets. The arrowhead indicates the TET8‐specific band that corresponds to the predicted molecular weight of the protein and is verified by probing a tet8 null mutant (Figure ). The prominent band in Ponceau S at 55 kDa is likely RBCL. For TEM, EV, extracellular vesicle; nf, nanofilament; sip, small irregular particle <50 nm in diameter. Arabidopsis expressing RFP‐PEN1, TET8‐GFP and GFP‐REMORIN1.3 (REM1.3) were used where indicated. P10 = pellet from 10,000 × g centrifugation of AWF; P40 = pellet from 40,000 × g centrifugation of P10 supernatant; P100‐40 = pellet from 100,000 × g centrifugation of P40 supernatant; P100 = pellet from 100,000 × g centrifugation from P10 supernatant (no 40,000 × g step); P400 = pellet from 400,000 × g centrifugation of P100 supernatant; S100 = supernatant after 100,000 × g centrifugation.
    Nanoparticle Tracker Particle Metrix Pmx 120 Zetaview Mono 488 Laser, supplied by Particle Metrix, 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/zetaview+particle+tracker/pmc12104214-107-1-3?v=Particle+Metrix
    Average 90 stars, based on 1 article reviews
    nanoparticle tracker particle metrix pmx 120 zetaview mono 488 laser - by Bioz Stars, 2026-07
    90/100 stars

    Images

    1) Product Images from "Arabidopsis Produces Distinct Subpopulations of Extracellular Vesicles That Respond Differentially to Biotic Stress, Altering Growth and Infectivity of a Fungal Pathogen"

    Article Title: Arabidopsis Produces Distinct Subpopulations of Extracellular Vesicles That Respond Differentially to Biotic Stress, Altering Growth and Infectivity of a Fungal Pathogen

    Journal: Journal of Extracellular Vesicles

    doi: 10.1002/jev2.70090

    40,000 × g is sufficient to pellet the majority of plant EVs. Immunoblots, nanoparticle tracking analysis (NTA), and representative transmission electron microscopy (TEM) images of the indicated extracellular fractions from Arabidopsis rosettes processed by differential ultracentrifugation, as indicated in the diagram. For immunoblots, samples are apoplastic wash fluid (AWF) and the indicated pellets collected from 5 mL of AWF. Numbers on the left sides of immunoblots indicate sizes in kiloDaltons. The TET8 antibody strongly cross‐reacts with a <25 kDa protein abundant in EV pellets. The arrowhead indicates the TET8‐specific band that corresponds to the predicted molecular weight of the protein and is verified by probing a tet8 null mutant (Figure ). The prominent band in Ponceau S at 55 kDa is likely RBCL. For TEM, EV, extracellular vesicle; nf, nanofilament; sip, small irregular particle <50 nm in diameter. Arabidopsis expressing RFP‐PEN1, TET8‐GFP and GFP‐REMORIN1.3 (REM1.3) were used where indicated. P10 = pellet from 10,000 × g centrifugation of AWF; P40 = pellet from 40,000 × g centrifugation of P10 supernatant; P100‐40 = pellet from 100,000 × g centrifugation of P40 supernatant; P100 = pellet from 100,000 × g centrifugation from P10 supernatant (no 40,000 × g step); P400 = pellet from 400,000 × g centrifugation of P100 supernatant; S100 = supernatant after 100,000 × g centrifugation.
    Figure Legend Snippet: 40,000 × g is sufficient to pellet the majority of plant EVs. Immunoblots, nanoparticle tracking analysis (NTA), and representative transmission electron microscopy (TEM) images of the indicated extracellular fractions from Arabidopsis rosettes processed by differential ultracentrifugation, as indicated in the diagram. For immunoblots, samples are apoplastic wash fluid (AWF) and the indicated pellets collected from 5 mL of AWF. Numbers on the left sides of immunoblots indicate sizes in kiloDaltons. The TET8 antibody strongly cross‐reacts with a <25 kDa protein abundant in EV pellets. The arrowhead indicates the TET8‐specific band that corresponds to the predicted molecular weight of the protein and is verified by probing a tet8 null mutant (Figure ). The prominent band in Ponceau S at 55 kDa is likely RBCL. For TEM, EV, extracellular vesicle; nf, nanofilament; sip, small irregular particle <50 nm in diameter. Arabidopsis expressing RFP‐PEN1, TET8‐GFP and GFP‐REMORIN1.3 (REM1.3) were used where indicated. P10 = pellet from 10,000 × g centrifugation of AWF; P40 = pellet from 40,000 × g centrifugation of P10 supernatant; P100‐40 = pellet from 100,000 × g centrifugation of P40 supernatant; P100 = pellet from 100,000 × g centrifugation from P10 supernatant (no 40,000 × g step); P400 = pellet from 400,000 × g centrifugation of P100 supernatant; S100 = supernatant after 100,000 × g centrifugation.

    Techniques Used: Western Blot, Transmission Assay, Electron Microscopy, Molecular Weight, Mutagenesis, Expressing, Centrifugation



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    40,000 × g is sufficient to pellet the majority of plant EVs. Immunoblots, <t>nanoparticle</t> tracking analysis (NTA), and representative transmission electron microscopy (TEM) images of the indicated extracellular fractions from Arabidopsis rosettes processed by differential ultracentrifugation, as indicated in the diagram. For immunoblots, samples are apoplastic wash fluid (AWF) and the indicated pellets collected from 5 mL of AWF. Numbers on the left sides of immunoblots indicate sizes in kiloDaltons. The TET8 antibody strongly cross‐reacts with a <25 kDa protein abundant in EV pellets. The arrowhead indicates the TET8‐specific band that corresponds to the predicted molecular weight of the protein and is verified by probing a tet8 null mutant (Figure ). The prominent band in Ponceau S at 55 kDa is likely RBCL. For TEM, EV, extracellular vesicle; nf, nanofilament; sip, small irregular particle <50 nm in diameter. Arabidopsis expressing RFP‐PEN1, TET8‐GFP and GFP‐REMORIN1.3 (REM1.3) were used where indicated. P10 = pellet from 10,000 × g centrifugation of AWF; P40 = pellet from 40,000 × g centrifugation of P10 supernatant; P100‐40 = pellet from 100,000 × g centrifugation of P40 supernatant; P100 = pellet from 100,000 × g centrifugation from P10 supernatant (no 40,000 × g step); P400 = pellet from 400,000 × g centrifugation of P100 supernatant; S100 = supernatant after 100,000 × g centrifugation.
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    Image Search Results


    40,000 × g is sufficient to pellet the majority of plant EVs. Immunoblots, nanoparticle tracking analysis (NTA), and representative transmission electron microscopy (TEM) images of the indicated extracellular fractions from Arabidopsis rosettes processed by differential ultracentrifugation, as indicated in the diagram. For immunoblots, samples are apoplastic wash fluid (AWF) and the indicated pellets collected from 5 mL of AWF. Numbers on the left sides of immunoblots indicate sizes in kiloDaltons. The TET8 antibody strongly cross‐reacts with a <25 kDa protein abundant in EV pellets. The arrowhead indicates the TET8‐specific band that corresponds to the predicted molecular weight of the protein and is verified by probing a tet8 null mutant (Figure ). The prominent band in Ponceau S at 55 kDa is likely RBCL. For TEM, EV, extracellular vesicle; nf, nanofilament; sip, small irregular particle <50 nm in diameter. Arabidopsis expressing RFP‐PEN1, TET8‐GFP and GFP‐REMORIN1.3 (REM1.3) were used where indicated. P10 = pellet from 10,000 × g centrifugation of AWF; P40 = pellet from 40,000 × g centrifugation of P10 supernatant; P100‐40 = pellet from 100,000 × g centrifugation of P40 supernatant; P100 = pellet from 100,000 × g centrifugation from P10 supernatant (no 40,000 × g step); P400 = pellet from 400,000 × g centrifugation of P100 supernatant; S100 = supernatant after 100,000 × g centrifugation.

    Journal: Journal of Extracellular Vesicles

    Article Title: Arabidopsis Produces Distinct Subpopulations of Extracellular Vesicles That Respond Differentially to Biotic Stress, Altering Growth and Infectivity of a Fungal Pathogen

    doi: 10.1002/jev2.70090

    Figure Lengend Snippet: 40,000 × g is sufficient to pellet the majority of plant EVs. Immunoblots, nanoparticle tracking analysis (NTA), and representative transmission electron microscopy (TEM) images of the indicated extracellular fractions from Arabidopsis rosettes processed by differential ultracentrifugation, as indicated in the diagram. For immunoblots, samples are apoplastic wash fluid (AWF) and the indicated pellets collected from 5 mL of AWF. Numbers on the left sides of immunoblots indicate sizes in kiloDaltons. The TET8 antibody strongly cross‐reacts with a <25 kDa protein abundant in EV pellets. The arrowhead indicates the TET8‐specific band that corresponds to the predicted molecular weight of the protein and is verified by probing a tet8 null mutant (Figure ). The prominent band in Ponceau S at 55 kDa is likely RBCL. For TEM, EV, extracellular vesicle; nf, nanofilament; sip, small irregular particle <50 nm in diameter. Arabidopsis expressing RFP‐PEN1, TET8‐GFP and GFP‐REMORIN1.3 (REM1.3) were used where indicated. P10 = pellet from 10,000 × g centrifugation of AWF; P40 = pellet from 40,000 × g centrifugation of P10 supernatant; P100‐40 = pellet from 100,000 × g centrifugation of P40 supernatant; P100 = pellet from 100,000 × g centrifugation from P10 supernatant (no 40,000 × g step); P400 = pellet from 400,000 × g centrifugation of P100 supernatant; S100 = supernatant after 100,000 × g centrifugation.

    Article Snippet: The nanoparticle tracker (Particle Metrix PMX 120 Zetaview Mono 488 Laser running Zetaview software version 8.05.16 SP3) was calibrated with 100 nm beads (nanoComposix silica nanospheres #SISN100).

    Techniques: Western Blot, Transmission Assay, Electron Microscopy, Molecular Weight, Mutagenesis, Expressing, Centrifugation