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Nacalai serum albumin bsa
Characteristics of large-diameter carbon nanotubes (Ld-CNTs) and small-diameter carbon nanotubes (Sd-CNTs). Transmission electron microscopy (TEM) images of Ld-CNTs (a), Sd-CNTs (b), and dispersions of Ld-CNTs (c) and Sd-CNTs (d) in <t>BSA.</t>
Serum Albumin Bsa, supplied by Nacalai, used in various techniques. Bioz Stars score: 92/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/serum albumin bsa/product/Nacalai
Average 92 stars, based on 4 article reviews
Price from $9.99 to $1999.99
serum albumin bsa - by Bioz Stars, 2022-10
92/100 stars

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1) Product Images from "Clearance of single-wall carbon nanotubes from the mouse lung: a quantitative evaluation †"

Article Title: Clearance of single-wall carbon nanotubes from the mouse lung: a quantitative evaluation †

Journal: Nanoscale Advances

doi: 10.1039/d0na00040j

Characteristics of large-diameter carbon nanotubes (Ld-CNTs) and small-diameter carbon nanotubes (Sd-CNTs). Transmission electron microscopy (TEM) images of Ld-CNTs (a), Sd-CNTs (b), and dispersions of Ld-CNTs (c) and Sd-CNTs (d) in BSA.
Figure Legend Snippet: Characteristics of large-diameter carbon nanotubes (Ld-CNTs) and small-diameter carbon nanotubes (Sd-CNTs). Transmission electron microscopy (TEM) images of Ld-CNTs (a), Sd-CNTs (b), and dispersions of Ld-CNTs (c) and Sd-CNTs (d) in BSA.

Techniques Used: Transmission Assay, Electron Microscopy, Transmission Electron Microscopy

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  • bsa  (Nacalai)
    88
    Nacalai bsa
    Virucidal activities of <t>MGDG</t> and sodium hypochlorite (NaClO) against FCV in the presence of bovine serum albumin <t>(BSA).</t> FCV (2 × 10 5 PFU/mL) was mixed with an equal volume of 0 and 100 μg/mL MGDG or NaClO in the presence of 0%, 2%, and 5% BSA and incubated for the indicated time at 37 °C. Results are expressed as the percentages of residual infectivity of MGDG-treated virus compared to the residual infectivity of the mock-treated virus control. Data are the means from independent duplicate assays.
    Bsa, supplied by Nacalai, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/bsa/product/Nacalai
    Average 88 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    bsa - by Bioz Stars, 2022-10
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    90
    Nacalai fitc labeled bovine serum albumin
    M protein, N protein, and RNA interactions. a Differential interference contrast (DIC) and fluorescence images of liquid-liquid phase separation (LLPS) of N protein <t>(TAMRA-labeled)</t> with or without M protein <t>(FITC-labeled).</t> The experiment was repeated three times with similar results. b FLAG tag pull-down assay using recombinant M protein (FLAG-tagged) and N protein (no tag) in the absence or presence of poly(I:C). The experiment was repeated twice with similar results. Source data are provided as a Source Data file. c StrepII tag pull-down assay using recombinant N protein (StrepII-tagged) and M protein (FLAG-tagged) in the absence or presence of RNAs of different sizes. RNA-H and RNA-L indicate yeast RNA with molecular weights > 30 kDa and 3–30 kDa, respectively. The experiment was repeated twice with similar results. d Electrostatic surface potentials of the intravirion side of the M protein dimer (long form). Positively charged residues to which the mutations were introduced in e are shown using stick representations and labeled. e Co-immunoprecipitation assay of wild-type (WT) or mutant M proteins with N protein in HEK293T cells. The experiment was repeated three times with similar results. Source data are provided as a Source Data file. f Model of M protein-triggered SARS-CoV-2 assembly M protein in the endoplasmic reticulum–Golgi intermediate compartment (ERGIC) forms dimers in two different conformations that assemble into higher-order oligomers to induce membrane curvature. M protein recruits N and genomic RNA in a cooperative manner. S and E proteins are also recruited to the budding site via an unknown mechanism. Source data are provided as a Source Data file.
    Fitc Labeled Bovine Serum Albumin, supplied by Nacalai, 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/result/fitc labeled bovine serum albumin/product/Nacalai
    Average 90 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    fitc labeled bovine serum albumin - by Bioz Stars, 2022-10
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    92
    Nacalai serum albumin bsa
    Characteristics of large-diameter carbon nanotubes (Ld-CNTs) and small-diameter carbon nanotubes (Sd-CNTs). Transmission electron microscopy (TEM) images of Ld-CNTs (a), Sd-CNTs (b), and dispersions of Ld-CNTs (c) and Sd-CNTs (d) in <t>BSA.</t>
    Serum Albumin Bsa, supplied by Nacalai, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/serum albumin bsa/product/Nacalai
    Average 92 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    serum albumin bsa - by Bioz Stars, 2022-10
    92/100 stars
      Buy from Supplier

    Image Search Results


    Virucidal activities of MGDG and sodium hypochlorite (NaClO) against FCV in the presence of bovine serum albumin (BSA). FCV (2 × 10 5 PFU/mL) was mixed with an equal volume of 0 and 100 μg/mL MGDG or NaClO in the presence of 0%, 2%, and 5% BSA and incubated for the indicated time at 37 °C. Results are expressed as the percentages of residual infectivity of MGDG-treated virus compared to the residual infectivity of the mock-treated virus control. Data are the means from independent duplicate assays.

    Journal: Marine Drugs

    Article Title: Virucidal and Immunostimulating Activities of Monogalactosyl Diacylglyceride from Coccomyxa sp. KJ, a Green Microalga, against Murine Norovirus and Feline Calicivirus

    doi: 10.3390/md20020131

    Figure Lengend Snippet: Virucidal activities of MGDG and sodium hypochlorite (NaClO) against FCV in the presence of bovine serum albumin (BSA). FCV (2 × 10 5 PFU/mL) was mixed with an equal volume of 0 and 100 μg/mL MGDG or NaClO in the presence of 0%, 2%, and 5% BSA and incubated for the indicated time at 37 °C. Results are expressed as the percentages of residual infectivity of MGDG-treated virus compared to the residual infectivity of the mock-treated virus control. Data are the means from independent duplicate assays.

    Article Snippet: The virucidal effects of MGDG on FCV were examined in the presence of an organic substance, BSA (Nacalai Tesque), and compared with those of NaClO, which is frequently used as a disinfectant.

    Techniques: Incubation, Infection

    Higher cell adhesion ability in AML cell lines with EVI1 high expression. A . The expression of four integrin genes (ITGB1, ITGB4, ITGA4 and ITGA6), EVI1 and b-actin as a control was determined by semiquantitative RT-PCR in three different EVI1 low and EVI1 high AML cell lines and two primary AML cells lines with high EVI1 expression (PT9 and PT11). B . Six AML cell lines with low or high EVI1expression, as indicated in the figure, were incubated in culture medium on BSA, collagen, fibronectin, laminin or matrigel-coated plates; the percentage of the total number of incubated cells that adhered to the plates was designated as the binding activity (%). Each experiment was performed in triplicate, and the experiments were independently repeated at least three times. The data are given the as the mean ± standard error (S.E). The statistical analysis was performed using the Student's t-test (* p

    Journal: PLoS ONE

    Article Title: The Increased Expression of Integrin ?6 (ITGA6) Enhances Drug Resistance in EVI1high Leukemia

    doi: 10.1371/journal.pone.0030706

    Figure Lengend Snippet: Higher cell adhesion ability in AML cell lines with EVI1 high expression. A . The expression of four integrin genes (ITGB1, ITGB4, ITGA4 and ITGA6), EVI1 and b-actin as a control was determined by semiquantitative RT-PCR in three different EVI1 low and EVI1 high AML cell lines and two primary AML cells lines with high EVI1 expression (PT9 and PT11). B . Six AML cell lines with low or high EVI1expression, as indicated in the figure, were incubated in culture medium on BSA, collagen, fibronectin, laminin or matrigel-coated plates; the percentage of the total number of incubated cells that adhered to the plates was designated as the binding activity (%). Each experiment was performed in triplicate, and the experiments were independently repeated at least three times. The data are given the as the mean ± standard error (S.E). The statistical analysis was performed using the Student's t-test (* p

    Article Snippet: A culture plate was coated overnight with a 1/40 dilution of Growth Factor Reduced-Matrigel (BD Falcon), 5 mg/cm2 of fibronectin (BD Falcon), 5 mg/cm2 of laminin (BD Falcon), 0.3 mg/ml of collagen (Nitta Gelatin) or 5% w/v BSA (Nacalai Tesque).

    Techniques: Expressing, Reverse Transcription Polymerase Chain Reaction, Incubation, Binding Assay, Activity Assay

    M protein, N protein, and RNA interactions. a Differential interference contrast (DIC) and fluorescence images of liquid-liquid phase separation (LLPS) of N protein (TAMRA-labeled) with or without M protein (FITC-labeled). The experiment was repeated three times with similar results. b FLAG tag pull-down assay using recombinant M protein (FLAG-tagged) and N protein (no tag) in the absence or presence of poly(I:C). The experiment was repeated twice with similar results. Source data are provided as a Source Data file. c StrepII tag pull-down assay using recombinant N protein (StrepII-tagged) and M protein (FLAG-tagged) in the absence or presence of RNAs of different sizes. RNA-H and RNA-L indicate yeast RNA with molecular weights > 30 kDa and 3–30 kDa, respectively. The experiment was repeated twice with similar results. d Electrostatic surface potentials of the intravirion side of the M protein dimer (long form). Positively charged residues to which the mutations were introduced in e are shown using stick representations and labeled. e Co-immunoprecipitation assay of wild-type (WT) or mutant M proteins with N protein in HEK293T cells. The experiment was repeated three times with similar results. Source data are provided as a Source Data file. f Model of M protein-triggered SARS-CoV-2 assembly M protein in the endoplasmic reticulum–Golgi intermediate compartment (ERGIC) forms dimers in two different conformations that assemble into higher-order oligomers to induce membrane curvature. M protein recruits N and genomic RNA in a cooperative manner. S and E proteins are also recruited to the budding site via an unknown mechanism. Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: Structure of SARS-CoV-2 membrane protein essential for virus assembly

    doi: 10.1038/s41467-022-32019-3

    Figure Lengend Snippet: M protein, N protein, and RNA interactions. a Differential interference contrast (DIC) and fluorescence images of liquid-liquid phase separation (LLPS) of N protein (TAMRA-labeled) with or without M protein (FITC-labeled). The experiment was repeated three times with similar results. b FLAG tag pull-down assay using recombinant M protein (FLAG-tagged) and N protein (no tag) in the absence or presence of poly(I:C). The experiment was repeated twice with similar results. Source data are provided as a Source Data file. c StrepII tag pull-down assay using recombinant N protein (StrepII-tagged) and M protein (FLAG-tagged) in the absence or presence of RNAs of different sizes. RNA-H and RNA-L indicate yeast RNA with molecular weights > 30 kDa and 3–30 kDa, respectively. The experiment was repeated twice with similar results. d Electrostatic surface potentials of the intravirion side of the M protein dimer (long form). Positively charged residues to which the mutations were introduced in e are shown using stick representations and labeled. e Co-immunoprecipitation assay of wild-type (WT) or mutant M proteins with N protein in HEK293T cells. The experiment was repeated three times with similar results. Source data are provided as a Source Data file. f Model of M protein-triggered SARS-CoV-2 assembly M protein in the endoplasmic reticulum–Golgi intermediate compartment (ERGIC) forms dimers in two different conformations that assemble into higher-order oligomers to induce membrane curvature. M protein recruits N and genomic RNA in a cooperative manner. S and E proteins are also recruited to the budding site via an unknown mechanism. Source data are provided as a Source Data file.

    Article Snippet: FITC-labeled bovine serum albumin (BSA, Nacalai tesque) was prepared similarly to FITC-labeled M protein.

    Techniques: Fluorescence, Labeling, FLAG-tag, Pull Down Assay, Recombinant, Co-Immunoprecipitation Assay, Mutagenesis

    Characteristics of large-diameter carbon nanotubes (Ld-CNTs) and small-diameter carbon nanotubes (Sd-CNTs). Transmission electron microscopy (TEM) images of Ld-CNTs (a), Sd-CNTs (b), and dispersions of Ld-CNTs (c) and Sd-CNTs (d) in BSA.

    Journal: Nanoscale Advances

    Article Title: Clearance of single-wall carbon nanotubes from the mouse lung: a quantitative evaluation †

    doi: 10.1039/d0na00040j

    Figure Lengend Snippet: Characteristics of large-diameter carbon nanotubes (Ld-CNTs) and small-diameter carbon nanotubes (Sd-CNTs). Transmission electron microscopy (TEM) images of Ld-CNTs (a), Sd-CNTs (b), and dispersions of Ld-CNTs (c) and Sd-CNTs (d) in BSA.

    Article Snippet: Ld-CNTs or Sd-CNTs were dispersed in aqueous solutions of bovine serum albumin (BSA) (Nacalai Tesque, Kyoto, Japan).

    Techniques: Transmission Assay, Electron Microscopy, Transmission Electron Microscopy