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AIF Antibody抗体,orb1239191,bior

byt
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  • ¥3770
  • biorbyt已认证
  • orb1239191
  • 英国
  • 2025年12月08日
  • ELISA, IF, WB
  • Human
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体名

      AIF Antibody抗体

    • 抗体英文名

      AIF Antibody

    • 靶点

      AIFM1

    • 浓度

      1 mg/ml

    • 应用范围

      ELISA, IF, WB

    • 适应物种

      Human

    • 保质期

      6-12个月

    • 抗原来源

      详询

    • 目录编号

      orb1239191

    • 级别

      科研级

    • 库存

      88

    • 供应商

      biorbyt

    • 标记物

      Unconjugated

    • 克隆性

      Polyclonal

    • 形态

      Liquid

    • 亚型

      IgG

    • 免疫原

      Anti-AIF antibody (orb1239191) was raised against a peptide corresponding to 14 amino acids near the amino terminus of mature human AIF. The immunogen is located within amino acids 90-140 of AIF.

    • 规格

      0.02 mg

    产品描述:AIF Antibody

    别名:AIF Antibody: Apoptosis-inducing factor 1, Programmed cell death protein 8, AIF, PDCD8

    免疫原:Anti-AIF antibody (orb1239191) was raised against a peptide corresponding to 14 amino acids near the amino terminus of mature human AIF. The 免疫原 is located within amino acids 90-140 of AIF.

    预测反应性:Mouse, Rat

    分子量:Predicted: 67 kDa Observed: 68 kDa

    防腐剂:AIF Antibody is supplied in PBS containing 0.02% sodium azide.

    纯化:AIF Antibody is Ion exchange chromatography purified.

    保存说明:Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.

    NCBI:O95381

    UniProt ID:O95381

    Note:For research use only.

    产品细节图片1
    Western Blot Validation in Human Cell Lines. Loading: 15 µg of lysates per lane. Antibodies: AIF orb1239191, (1 µg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.

    产品细节图片2
    Independent Antibody Validation (IAV) via Protein Expression Profile in Cell Lines. Loading: 15 µg of lysates per lane. Antibodies: AIF orb1239169, (1 µg/mL), AIF orb1239191, (1 µg/mL), AIF orb1239168, (2 µg/mL), and beta-actin (1 µg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.

    产品细节图片3
    Immunofluorescence Validation of AIF in K562 Cells. Immunofluorescent analysis of 4% Fixative-fixed K562 Cells labeling AIF with orb1239191 at 20 µg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green).

    产品细节图片4
    KD and Induced Validation of AIF in H1299 Cells (Stambolsky et al., 2006). Western blot analysis of AIF knockdown with anti-AIF antibodies in H1299 cells. AIF expression was disrupted in AIF knockdown cells (siRNA1 and siRNA4). An increased expression of AIF was induced by ZnCl2 treatment, which was not observed in AIF knockdown cells.

    产品细节图片5
    KD Validation of AIF in AIF Silenced Stable Cells (Apostolova et al., 2006). AIF silencing is sustained in stable cell lines. Western blot analysis ofstable lines AIF-1-10, AIF-2-4 and pU6-2 using anti-AIF antibodies. AIF protein was disrupted after AIF silencing with AIF siRNA (AIF-1-10 and AIF-2-4) as compared to control (Hep3B and pU6-2).

    产品细节图片6
    Immunofluorescence Validation of AIF in Rat Hippocampal Neurons (Hofer et al., 2011). (G-L) After exposure to bacterial components, AIF colocalized in mature neurons (MAP2; I, L), immature neurons (DcX; H, K), and stem/progenitor cells (Nestin; G, J). AIF expression was detected by anti-AIF antibodies.

    产品细节图片7
    Subcellular Localization Validation of AIF in mononuclear cells (Gupta et al., 2003). A shows mononuclear cells (MNCs) alone, B shows MNCs transfected with control plasmid, C shows MNCs transfected with Bcl-2 expression plasmid. Overlay is of Mitotracker (red) and AIF (green). Hoechst 33258 dye is used to examine chromatin fragmentation. The release of AIF form mitochondria is detected by anti-AIF antibodies.

    产品细节图片8
    Induced Expression Validation of AIF in U937 Cells (Ikai et al., 2006). Release of AIF at 48 h after the treatment with 30 uM magnolol examined by Western blotAnalysis with anti-AIF antibodies. AIF release was markedly increased 48h after magnolol treatment.

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    图标文献和实验
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      zj000718 想请问各位大虾 如果损伤致凋亡模型中,经典凋亡途径(caspase-3为代表)表达很好,还会有AIF等非caspase依赖性通路存在吗?(怎么验证他们之间是否存在交互效应呢) 如果想从体内抑制caspase通路 什么方法比较可靠呢?基因敲除、局部注射siRNA、局部注射广谱caspase通路抑制剂???是否有比较确切的方法呢???请做过这方面研究的大神们指教,谢谢!!! freecell http

    • 【求助】请教一下核蛋白的提取

      宝贝儿妮妮 请教各位大虾,我做的是AIF(凋亡诱导因子),激活后从胞浆释放到胞核,与DNA结合,引起DNA的片段化 那我是不是必须得提取核蛋白,来证实发生了核转位?要怎么来提取效果好一点?时间紧急啊,非常感谢 lily628 买抽提核蛋白的试剂盒,国内的或国外的都行. xhjggl 上海生工有 021-37772436 细胞核蛋白质提取试剂盒

    • 线粒体和凋亡

      和执行中非常重要的分子,但某些蛋白质从线粒体内膜腔释放而诱导的凋亡可以不通过caspase产生,称为caspase非依赖性通路。成熟型的丝氨酸蛋白激酶Omi(iV-名HtrA2),在凋亡发生时和Smac一起从线粒体释放到细胞质,一方面灭活1AP,释放caspase,对凋亡复合体起辅助作用,促进凋亡的发生(caspase依赖性通路);另一方面通过其丝氨酸酶活性来激活凋亡,称为caspase非依赖性通路。此外,凋亡诱导因子(apoptosis inducing factor,AIF)位于线粒体的内膜腔内

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