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Anti-nNOS (neuronal) antibody

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100ug
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产品详情
  • 产品名称

    Anti-nNOS (neuronal)抗体
    参阅全部 nNOS (neuronal) 一抗

  • 描述

    兔多克隆抗体to nNOS (neuronal)

  • 宿主

    Rabbit

  • 经测试应用

    适用于: ICC/IFWBIHC-Pmore details

  • 种属反应性

    与反应: Mouse, Rat, Human
    预测可用于: Rabbit, Xenopus laevis, Zebrafish

  • 免疫原

    Synthetic peptide corresponding to Human nNOS (neuronal) aa 1411-1425.
    Sequence:

    NRLRSESIAFIEESK


    (Peptide available as ab5891)

    Run BLAST with BLAST the sequence with ExPASyRun BLAST with BLAST the sequence with NCBI

  • 常规说明


    The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.

    If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As

  • 形式

    Liquid

  • 存放说明

    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.

  • 存储溶液

    Preservative: 0.05% Sodium azide
    Constituents: 0.1% BSA, 99% PBS

  • 纯度

    Immunogen affinity purified

  • 克隆

    多克隆

  • 同种型

    IgG

The Abpromise guarantee

Abpromise™承诺保证使用ab5586于以下的经测试应用

“应用说明”部分 下显示的仅为推荐的起始稀释度;实际最佳的稀释度/浓度应由使用者检定。

应用Ab评论说明
ICC/IF

1/50 - 1/500.

WB

1/100 - 1/1000. Predicted molecular weight: 160 kDa.

IHC-P(1)

1/20 - 1/200.

数据库链接

别名

  • 2310005C01Rik antibody

  • BNOS antibody

  • Constitutive NOS antibody

  • EC 1.14.13.39 antibody

  • IHPS 1 antibody

  • IHPS1 antibody

  • N-NOS antibody

  • NC-NOS antibody

  • neuronal Nitric Oxide Synthase antibody

  • Neuronal NOS antibody

  • Nitric oxide synthase , neuronal, included antibody

  • Nitric oxide synthase 1 (neuronal) antibody

  • Nitric oxide synthase 1 antibody

  • Nitric oxide synthase, brain antibody

  • Nitric oxide synthase, penile neuronal, included antibody

  • NNOS antibody

  • NO antibody

  • NOS 1 antibody

  • NOS antibody

  • NOS type I antibody

  • NOS-I antibody

  • NOS1 antibody

  • NOS1_HUMAN antibody

  • Peptidyl-cysteine S-nitrosylase NOS1 antibody

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-nNOS (neuronal) antibody (ab5586)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-nNOS (neuronal) antibody (ab5586)

    ab5586 labelling nNOS (neuronal) in the cytoplasm of Mouse heart tissue (right) compared with a negative control (left) by Immunohistochemistry (formalin/PFA-fixed paraffin-embedded sections). To expose target proteins, antigen retrieval method was performed using 10mM sodium citrate (pH 6.0) microwaved for 8-15 min. Following antigen retrieval, tissues were blocked in 3% H2O2-methanol for 15 min at room temperature. Tissue sections were incubated with the primary antibody (1:20 in 3% BSA-PBS) overnight at 4°C. A HRP-conjugated anti-rabbit IgG was used as the secondary antibody, followed by colorimetric detection using a DAB kit. Tissues were counterstained with hematoxylin and dehydrated with ethanol and xylene to prep for mounting.

  • Immunocytochemistry/ Immunofluorescence - Anti-nNOS (neuronal) antibody (ab5586)

    Immunocytochemistry/ Immunofluorescence - Anti-nNOS (neuronal) antibody (ab5586)

    Immunocytochemistry/Immunofluorescence analysis of nNOS (neuronal) (green) showing staining in the cytoplasm and membrane of U251 cells (right) compared to a negative control without primary antibody (left). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with ab5586 in 3% BSA-PBS at a dilution of 1:100 and incubated overnight at 4ºC in a humidified chamber. Cells were washed with PBST and incubated with a DyLight-conjugated secondary antibody in PBS at room temperature in the dark. F-actin (red) was stained with a fluorescent red phalloidin and nuclei (blue) were stained with Hoechst or DAPI. Images were taken at a magnification of 60x.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-nNOS (neuronal) antibody (ab5586)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-nNOS (neuronal) antibody (ab5586)

    ab5586 labelling nNOS (neuronal) in the cytoplasm of Human testis tissue (right) compared with a negative control (left) by Immunohistochemistry (formalin/PFA-fixed paraffin-embedded sections). To expose target proteins, antigen retrieval method was performed using 10mM sodium citrate (pH 6.0) microwaved for 8-15 min. Following antigen retrieval, tissues were blocked in 3% H2O2-methanol for 15 min at room temperature. Tissue sections were incubated with the primary antibody (1:200 in 3% BSA-PBS) overnight at 4°C. A HRP-conjugated anti-rabbit IgG was used as the secondary antibody, followed by colorimetric detection using a DAB kit. Tissues were counterstained with hematoxylin and dehydrated with ethanol and xylene to prep for mounting.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-nNOS (neuronal) antibody (ab5586)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-nNOS (neuronal) antibody (ab5586)

    ab5586 labelling nNOS (neuronal) in the cytoplasm of Human skeletal muscle (right) compared with a negative control (left) by Immunohistochemistry (formalin/PFA-fixed paraffin-embedded sections). To expose target proteins, antigen retrieval method was performed using 10mM sodium citrate (pH 6.0) microwaved for 8-15 min. Following antigen retrieval, tissues were blocked in 3% H2O2-methanol for 15 min at room temperature. Tissue sections were incubated with the primary antibody (1:200 in 3% BSA-PBS) overnight at 4°C. A HRP-conjugated anti-rabbit IgG was used as the secondary antibody, followed by colorimetric detection using a DAB kit. Tissues were counterstained with hematoxylin and dehydrated with ethanol and xylene to prep for mounting.

  • Western blot - Anti-nNOS (neuronal) antibody (ab5586)

    Western blot - Anti-nNOS (neuronal) antibody (ab5586)

    Anti-nNOS (neuronal) antibody (ab5586) at 1/500 dilution + Mouse brain cell lysate at 25 µg

    Predicted band size: 160 kDa
    Observed band size: 160 kDa

  • Western blot - Anti-nNOS (neuronal) antibody (ab5586)

    Western blot - Anti-nNOS (neuronal) antibody (ab5586)

    Anti-nNOS (neuronal) antibody (ab5586) at 1/200 dilution + Rat brain cell lysate at 25 µg

    Predicted band size: 160 kDa
    Observed band size: 160 kDa