anti neurexin 1α extracellular atto 488 antibody  (Alomone Labs)


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    Name:
    Anti Neurexin 1alpha extracellular ATTO Fluor 488 Antibody
    Description:
    Anti Neurexin 1α extracellular Antibody ANR 031 is a highly specific antibody directed against an extracellular epitope of the rat protein The antibody can be used in western blot and live cell imaging applications It has been designed to recognize Nrxn1α from rat mouse and human samples nAnti Neurexin 1α extracellular ATTO 488 Antibody ANR 031 AG is directly labeled with an ATTO 488 fluorescent dye ATTO dyes are characterized by strong absorption high extinction coefficient high fluorescence quantum yield and high photo stability The ATTO 488 label is analogous to the well known dye fluorescein isothiocyanate FITC and can be used with filters typically used to detect FITC Anti Neurexin 1α extracellular ATTO 488 Antibody has been tested in immunohistochemistry applications and is especially suited for experiments requiring simultaneous labeling of different markers
    Catalog Number:
    ANR-031-AG
    Price:
    686.0
    Category:
    Primary Antibody
    Applications:
    Immunofluorescence, Immunohistochemistry
    Purity:
    Affinity purified on immobilized antigen.
    Immunogen:
    Synthetic peptide
    Size:
    50 mcl
    Antibody Type:
    Polyclonal ATTO 488 (Green) Conjugated Primary Antibody
    Format:
    Lyophilized Powder
    Host:
    Rabbit
    Isotype:
    Rabbit IgG
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    Structured Review

    Alomone Labs anti neurexin 1α extracellular atto 488 antibody
    Anti Neurexin 1alpha extracellular ATTO Fluor 488 Antibody
    Anti Neurexin 1α extracellular Antibody ANR 031 is a highly specific antibody directed against an extracellular epitope of the rat protein The antibody can be used in western blot and live cell imaging applications It has been designed to recognize Nrxn1α from rat mouse and human samples nAnti Neurexin 1α extracellular ATTO 488 Antibody ANR 031 AG is directly labeled with an ATTO 488 fluorescent dye ATTO dyes are characterized by strong absorption high extinction coefficient high fluorescence quantum yield and high photo stability The ATTO 488 label is analogous to the well known dye fluorescein isothiocyanate FITC and can be used with filters typically used to detect FITC Anti Neurexin 1α extracellular ATTO 488 Antibody has been tested in immunohistochemistry applications and is especially suited for experiments requiring simultaneous labeling of different markers
    https://www.bioz.com/result/anti neurexin 1α extracellular atto 488 antibody/product/Alomone Labs
    Average 90 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti neurexin 1α extracellular atto 488 antibody - by Bioz Stars, 2021-09
    90/100 stars

    Images

    1) Product Images from "Mimicking Neuroligin-2 Functions in β-cells by Functionalized Nanoparticles as a Novel Approach for Antidiabetic Therapy"

    Article Title: Mimicking Neuroligin-2 Functions in β-cells by Functionalized Nanoparticles as a Novel Approach for Antidiabetic Therapy

    Journal: ACS applied materials & interfaces

    doi: 10.1021/acsami.6b10568

    Effect of HSA-28P and HSA-28 on the binding affinity of anti-Neurexin 1α antibody INS-1E cells that were seeded in 12-well plates. The cells were incubated with HSA-28P, “naked” nanoparticles or HSA-28 peptide for 24 h. After the indicated incubation time, cells were exposed to ATTO 488-fluorescent labeled antibody against an extracellular epitope of Neurexin 1α according to the manufacturer`s protocol. After then, cells were taken to Gallios Fluorescence Activated Cell Sorter. Control cells (A), treated only by anti-Neurexin 1α antibody ( B ), treated by HSA-28P and anti-Neurexin 1α antibody ( C ), treated by “naked” nanoparticles and anti-Neurexin 1α antibody ( D ) and finally cells treated by HSA-28 and anti-Neurexin 1α antibody ( E ). The summary of the spectra of the fluorescent signals (F). The summary of cell counts and percentage of the inhibition. n=3.
    Figure Legend Snippet: Effect of HSA-28P and HSA-28 on the binding affinity of anti-Neurexin 1α antibody INS-1E cells that were seeded in 12-well plates. The cells were incubated with HSA-28P, “naked” nanoparticles or HSA-28 peptide for 24 h. After the indicated incubation time, cells were exposed to ATTO 488-fluorescent labeled antibody against an extracellular epitope of Neurexin 1α according to the manufacturer`s protocol. After then, cells were taken to Gallios Fluorescence Activated Cell Sorter. Control cells (A), treated only by anti-Neurexin 1α antibody ( B ), treated by HSA-28P and anti-Neurexin 1α antibody ( C ), treated by “naked” nanoparticles and anti-Neurexin 1α antibody ( D ) and finally cells treated by HSA-28 and anti-Neurexin 1α antibody ( E ). The summary of the spectra of the fluorescent signals (F). The summary of cell counts and percentage of the inhibition. n=3.

    Techniques Used: Binding Assay, Incubation, Labeling, Fluorescence, Inhibition

    2) Product Images from "Mimicking Neuroligin-2 Functions in β-cells by Functionalized Nanoparticles as a Novel Approach for Antidiabetic Therapy"

    Article Title: Mimicking Neuroligin-2 Functions in β-cells by Functionalized Nanoparticles as a Novel Approach for Antidiabetic Therapy

    Journal: ACS applied materials & interfaces

    doi: 10.1021/acsami.6b10568

    Effect of HSA-28P and HSA-28 on the binding affinity of anti-Neurexin 1α antibody INS-1E cells that were seeded in 12-well plates. The cells were incubated with HSA-28P, “naked” nanoparticles or HSA-28 peptide for 24 h. After the indicated incubation time, cells were exposed to ATTO 488-fluorescent labeled antibody against an extracellular epitope of Neurexin 1α according to the manufacturer`s protocol. After then, cells were taken to Gallios Fluorescence Activated Cell Sorter. Control cells (A), treated only by anti-Neurexin 1α antibody ( B ), treated by HSA-28P and anti-Neurexin 1α antibody ( C ), treated by “naked” nanoparticles and anti-Neurexin 1α antibody ( D ) and finally cells treated by HSA-28 and anti-Neurexin 1α antibody ( E ). The summary of the spectra of the fluorescent signals (F). The summary of cell counts and percentage of the inhibition. n=3.
    Figure Legend Snippet: Effect of HSA-28P and HSA-28 on the binding affinity of anti-Neurexin 1α antibody INS-1E cells that were seeded in 12-well plates. The cells were incubated with HSA-28P, “naked” nanoparticles or HSA-28 peptide for 24 h. After the indicated incubation time, cells were exposed to ATTO 488-fluorescent labeled antibody against an extracellular epitope of Neurexin 1α according to the manufacturer`s protocol. After then, cells were taken to Gallios Fluorescence Activated Cell Sorter. Control cells (A), treated only by anti-Neurexin 1α antibody ( B ), treated by HSA-28P and anti-Neurexin 1α antibody ( C ), treated by “naked” nanoparticles and anti-Neurexin 1α antibody ( D ) and finally cells treated by HSA-28 and anti-Neurexin 1α antibody ( E ). The summary of the spectra of the fluorescent signals (F). The summary of cell counts and percentage of the inhibition. n=3.

    Techniques Used: Binding Assay, Incubation, Labeling, Fluorescence, Inhibition

    Related Articles

    other:

    Article Title: Mimicking Neuroligin-2 Functions in β-cells by Functionalized Nanoparticles as a Novel Approach for Antidiabetic Therapy
    Article Snippet: Anti-Neurexin 1α (extracellular)-ATTO-488 antibody was purchased from (Alomone Labs, Jerusalem, Israel) .

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  • 90
    Alomone Labs anti neurexin 1α extracellular atto 488 antibody
    Effect of HSA-28P and HSA-28 on the binding affinity of <t>anti-Neurexin</t> <t>1α</t> antibody INS-1E cells that were seeded in 12-well plates. The cells were incubated with HSA-28P, “naked” nanoparticles or HSA-28 peptide for 24 h. After the indicated incubation time, cells were exposed to ATTO 488-fluorescent labeled antibody against an extracellular epitope of Neurexin 1α according to the manufacturer`s protocol. After then, cells were taken to Gallios Fluorescence Activated Cell Sorter. Control cells (A), treated only by anti-Neurexin 1α antibody ( B ), treated by HSA-28P and anti-Neurexin 1α antibody ( C ), treated by “naked” nanoparticles and anti-Neurexin 1α antibody ( D ) and finally cells treated by HSA-28 and anti-Neurexin 1α antibody ( E ). The summary of the spectra of the fluorescent signals (F). The summary of cell counts and percentage of the inhibition. n=3.
    Anti Neurexin 1α Extracellular Atto 488 Antibody, supplied by Alomone Labs, 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/anti neurexin 1α extracellular atto 488 antibody/product/Alomone Labs
    Average 90 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti neurexin 1α extracellular atto 488 antibody - by Bioz Stars, 2021-09
    90/100 stars
      Buy from Supplier

    Image Search Results


    Effect of HSA-28P and HSA-28 on the binding affinity of anti-Neurexin 1α antibody INS-1E cells that were seeded in 12-well plates. The cells were incubated with HSA-28P, “naked” nanoparticles or HSA-28 peptide for 24 h. After the indicated incubation time, cells were exposed to ATTO 488-fluorescent labeled antibody against an extracellular epitope of Neurexin 1α according to the manufacturer`s protocol. After then, cells were taken to Gallios Fluorescence Activated Cell Sorter. Control cells (A), treated only by anti-Neurexin 1α antibody ( B ), treated by HSA-28P and anti-Neurexin 1α antibody ( C ), treated by “naked” nanoparticles and anti-Neurexin 1α antibody ( D ) and finally cells treated by HSA-28 and anti-Neurexin 1α antibody ( E ). The summary of the spectra of the fluorescent signals (F). The summary of cell counts and percentage of the inhibition. n=3.

    Journal: ACS applied materials & interfaces

    Article Title: Mimicking Neuroligin-2 Functions in β-cells by Functionalized Nanoparticles as a Novel Approach for Antidiabetic Therapy

    doi: 10.1021/acsami.6b10568

    Figure Lengend Snippet: Effect of HSA-28P and HSA-28 on the binding affinity of anti-Neurexin 1α antibody INS-1E cells that were seeded in 12-well plates. The cells were incubated with HSA-28P, “naked” nanoparticles or HSA-28 peptide for 24 h. After the indicated incubation time, cells were exposed to ATTO 488-fluorescent labeled antibody against an extracellular epitope of Neurexin 1α according to the manufacturer`s protocol. After then, cells were taken to Gallios Fluorescence Activated Cell Sorter. Control cells (A), treated only by anti-Neurexin 1α antibody ( B ), treated by HSA-28P and anti-Neurexin 1α antibody ( C ), treated by “naked” nanoparticles and anti-Neurexin 1α antibody ( D ) and finally cells treated by HSA-28 and anti-Neurexin 1α antibody ( E ). The summary of the spectra of the fluorescent signals (F). The summary of cell counts and percentage of the inhibition. n=3.

    Article Snippet: Anti-Neurexin 1α (extracellular)-ATTO-488 antibody was purchased from (Alomone Labs, Jerusalem, Israel) .

    Techniques: Binding Assay, Incubation, Labeling, Fluorescence, Inhibition