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Lipocalin-2/NGAL Recombinant Rabbit mAb (S-2280-129)

Neutrophil gelatinase-associated lipocalin,Lipocalin-2,Oncogene 24p3 (24p3),SV-40-induced 24p3 protein,Siderocalin LCN2,p25,Lcn2

价格 600.00 供应商现货 : 3-5个工作日
货号 S0B6437
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产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    Lipocalin-2/NGAL
  • 分子别名

    Neutrophil gelatinase-associated lipocalin; Lipocalin-2; Oncogene 24p3 (24p3); SV-40-induced 24p3 protein; Siderocalin LCN2; p25; Lcn2
  • 免疫原

    Synthetic Peptide
  • 细胞定位

    Secreted
  • Accession

    P11672
  • 克隆号

    S-2280-129
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 反应种属 ?

    Ms, Rt
  • 阳性样本

    mouse spleen, mouse bone marrow, mouse lung, rat spleen ,rat liver
  • 纯化方式

    Protein A
  • 浓度

    0.5 mg/ml
  • 标记

    Unconjugated
  • 性状

    Liquid
  • 缓冲体系

    PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300

  • 储存条件

    12 months from date of receipt / reconstitution, -20 °C as supplied

  • 应用

    IHC-P ?

    WB

    IF ?

  • 稀释度

    应用 稀释度 推荐种属
    WB 1:1000 Ms, Rt
    IHC-P 1:2000 Ms, Rt
    IF 1:500 Ms, Rt
背景介绍
  • Lipocalin-2/NGAL is a 25-kDa secreted glycoprotein of the lipocalin superfamily that forms an 8-stranded β-barrel calyx able to bind and transport ferric siderophore complexes, thereby acting as a bacteriostatic innate immune factor that starves bacteria of iron while simultaneously delivering iron to mammalian cells via the megalin/24p3R receptor, and is rapidly induced by inflammatory, hypoxic or nephrotoxic stress in neutrophils, macrophages and epithelia, circulates as monomer, homodimer or MMP-9–linked heterodimer, functions as a sensitive biomarker of acute and chronic kidney injury, modulates cell survival, differentiation, epithelial-to-mesenchymal transition and oncogenesis, and is transcriptionally up-regulated through NF-κB, ERK and JAK-STAT pathways in metabolic disorders such as obesity and insulin resistance.

  • 免疫印迹

    • WB result of Lipocalin-2/NGAL Recombinant Rabbit mAb
      Primary antibody: Lipocalin-2/NGAL Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: mouse heart lysate 20 µg
      Lane 2: mouse brain lysate 20 µg
      Lane 3: mouse spleen lysate 20 µg
      Lane 4: mouse bone marrow lysate 20 µg
      Lane 5: mouse lung lysate 20 µg
      Negative control: mouse heart lysate; mouse brain lysate
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 23 kDa
      Observed MW: 28 kDa

    • WB result of Lipocalin-2/NGAL Recombinant Rabbit mAb
      Primary antibody: Lipocalin-2/NGAL Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: rat heart lysate 20 µg
      Lane 2: rat spleen lysate 20 µg
      Lane 3: rat lung lysate 20 µg
      Negative control: rat heart lysate
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 23 kDa
      Observed MW: 28 kDa

  • 免疫组化

    • IHC shows positive staining in paraffin-embedded mouse spleen. Anti-Lipocalin-2/NGAL antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded mouse lung. Anti-Lipocalin-2/NGAL antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded mouse liver. Anti-Lipocalin-2/NGAL antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • Negative control: IHC shows negative staining in paraffin-embedded mouse cerebral cortex. Anti-Lipocalin-2/NGAL antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded rat spleen. Anti-Lipocalin-2/NGAL antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded rat lung. Anti-Lipocalin-2/NGAL antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded rat liver. Anti-Lipocalin-2/NGAL antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • Negative control: IHC shows negative staining in paraffin-embedded rat cerebral cortex. Anti-Lipocalin-2/NGAL antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

  • 免疫荧光

    • IF shows positive staining in paraffin-embedded mouse spleen. Anti- Lipocalin-2/NGAL antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • IF shows positive staining in paraffin-embedded mouse lung. Anti- Lipocalin-2/NGAL antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • IF shows negative staining in paraffin-embedded mouse brain. Anti- Lipocalin-2/NGAL antibody was used at 1/500 dilution and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • IF shows positive staining in paraffin-embedded rat spleen. Anti- Lipocalin-2/NGAL antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • IF shows positive staining in paraffin-embedded rat lung. Anti- Lipocalin-2/NGAL antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • IF shows negative staining in paraffin-embedded rat brain. Anti- Lipocalin-2/NGAL antibody was used at 1/500 dilution and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

  • 组织表达图谱

    • Expression of Lipocaliln-2/NGAL in mouse & rat tissue.

FAQs

斯达特公司的抗体,可以回收利用几次?

我们一般不推荐客户回收利用抗体。 因为抗体使用之后缓冲体系已经发生改变,不同客户在回收抗体的保存条件上也会有差异,所以抗体回收使用效果无法保证。另外,我们对一批抗体回收验证测试,测试结果显示不同抗体可回收次数不同,一般效价越高的抗体,可重复使用的次数越多,客户可根据实验情况来确定

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