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ASC凋亡相关斑点样蛋白ASC抗体

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  • ¥780 - 2200
  • LMAI Bio
  • LM-6741R
  • 进口/国产
  • 2025年12月23日
  • WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 Flow-Cyt=1ug/test IF=1:100-500 (石蜡切片需做抗原修复)
  • Rabbit
  • Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit,
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 供应商

      上海联迈生物工程有限公司

    • 库存

      大量

    • 目录编号

      LM-6741R

    • 克隆性

      多克隆

    • 抗原来源

      Rabbit

    • 保质期

      1年

    • 抗体英文名

      ASC

    • 抗体名

      凋亡相关斑点样蛋白ASC抗体

    • 宿主

      Rabbit

    • 适应物种

      Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit,

    • 免疫原

      KLH conjugated synthetic peptide derived from human TMS1/ASC:31-130/195

    • 亚型

      IgG

    • 形态

      Lyophilized or Liquid

    • 应用范围

      WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 Flow-Cyt=1ug/test IF=1:100-500 (石蜡切片需做抗原修复)

    • 浓度

      1mg/ml

    • 保存条件

      Store at -20 °C

    • 规格

      50ul  100ul  200ul

    ASC凋亡相关斑点样蛋白ASC抗体
    英文名称 ASC
    中文名称 凋亡相关斑点样蛋白ASC抗体
    别    名 TMS1; Apoptosis associated speck like protein containing a CARD; Apoptosis-associated speck-like protein containing a CARD; ASC_HUMAN; CARD 5; CARD5; Caspase recruitment domain containing protein 5; Caspase recruitment domain protein 5; Caspase recruitment domain-containing protein 5; hASC; MGC10332; PYCARD; TMS-1; PYD and CARD domain containing; PYD and CARD domain containing protein; PYD and CARD domain-containing protein; Target of methylation induced silencing 1; Target of methylation-induced silencing 1; TMS 1.  
    产品细节图片1 Specific References  (1)     |     bs-6741R has been referenced in 1 publications.
    [IF=3.06] Zhang, Bo, et al. "Cortistatin inhibits NLRP3 inflammasome activation of cardiac fibroblasts during sepsis." Journal of Cardiac Failure (2015).  WB ;  Rat.  
    PubMed:25639691
    规格价格 50ul/780元 购买    100ul/1380元 购买    200ul/2200元 购买    大包装/询价
    说 明 书 50ul  100ul  200ul
    研究领域 肿瘤  细胞生物  免疫学  信号转导  细胞凋亡  转录调节因子  肿瘤细胞生物标志物  
    抗体来源 Rabbit
    克隆类型 Polyclonal
    交叉反应 Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, 
    产品应用 WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 Flow-Cyt=1ug/test IF=1:100-500 (石蜡切片需做抗原修复) 
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量 22kDa
    细胞定位 细胞核 细胞浆 
    性    状 Lyophilized or Liquid
    浓    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human TMS1/ASC:31-130/195 
    亚    型 IgG
    纯化方法 affinity purified by Protein A
    储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
    PubMed PubMed
    产品介绍 background:
    Promotes caspase-mediated apoptosis. This proapoptotic activity is mediated predominantly through the activation of caspase-9. May be a component of the inflammasome, a protein complex which also includes NALP2, CARD8 and CASP1 and whose function would be the activation of proinflammatory caspases. Tissue specificity: Widely expressed at low levels. Detected in peripheral blood leukocytes, lung, small intestine, spleen, thymus, colon and at lower levels in placenta, liver and kidney. Very low expression in skeletal muscle, heart and brain. Detected in the leukemia cell lines HL-60 and U937, but not in Jurkat T-cell lymphoma and Daudi Burkitt's lymphoma.

    Function:
    Promotes caspase-mediated apoptosis. This proapoptotic activity is mediated predominantly through the activation of caspase-9. May be a component of the inflammasome, a protein complex which also includes NALP2, CARD8 and CASP1 and whose function would be the activation of proinflammatory caspases.

    Subunit:
    Forms complexes with other DAPIN domain-containing proteins. Interacts with CIAS1/PYPAF1 and PYDC1.

    Subcellular Location:
    Cytoplasm. Note=Upstream of caspase activation, a redistribution from the cytoplasm to the aggregates occurs. These appear as hollow, perinuclear spherical, ball-like structures.

    Tissue Specificity:
    Widely expressed at low levels. Detected in peripheral blood leukocytes, lung, small intestine, spleen, thymus, colon and at lower levels in placenta, liver and kidney. Very low expression in skeletal muscle, heart and brain. Detected in the leukemia cell lines HL-60 and U937, but not in Jurkat T-cell lymphoma and Daudi Burkitt's lymphoma. Detected in the melanoma cell line WM35, but not in WM793. Not detected in HeLa cervical carcinoma cells and Molt 4 lymphocytic leukemia cells.

    Post-translational modifications:
    Phosphorylated.

    Similarity:
    Contains 1 CARD domain.
    Contains 1 DAPIN domain. 

    SWISS:
    Q9ULZ3

    Gene ID:
    29108

    Database links:

    Entrez Gene: 29108 Human

    Omim: 606838 Human

    SwissProt: Q9ULZ3 Human

    Unigene: 499094 Human



    Important Note:
    This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 
     
    产品图片 产品细节图片2
    Sample:Spinal cord (Rat)Lysate at 40 ug
    Primary: Anti-ASC(bs-6741R)at 1/300 dilution
    Secondary: IRDye800CW Goat Anti-RabbitIgG at 1/20000 dilution
    Predicted band size: 22kD
    Observed band size: 18kD

    产品细节图片3
    Sample:Cerebrum (Rat)Lysate at 40 ug
    Primary: Anti-ASC(bs-6741R)at 1/300 dilution
    Secondary: IRDye800CW Goat Anti-RabbitIgG at 1/20000 dilution
    Predicted band size: 22kD
    Observed band size: 18kD

    产品细节图片4
    Paraformaldehyde-fixed, paraffin embedded (human gastric carcinoma); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (ASC) Polyclonal Antibody, Unconjugated (bs-6741R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
    产品细节图片5
    Paraformaldehyde-fixed, paraffin embedded (mouse brain tissue); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (ASC) Polyclonal Antibody, Unconjugated (bs-6741R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
    产品细节图片6
    Tissue/cell: Mouse spleen tissue; 4% Paraformaldehyde-fixed and paraffin-embedded; 
    Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min; 
    Incubation: Anti-ASC Polyclonal Antibody, Unconjugated(bs-6741R) 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining

    产品细节图片7
    Blank control:A549. 
    Primary Antibody (green line): Rabbit Anti-ASC antibody (bs-6741R) 
    Dilution: 1μg /10^6 cells; 
    Isotype Control Antibody (orange line): Rabbit IgG .
    Secondary Antibody : Goat anti-rabbit IgG-PE
    Dilution: 1μg /test. 
    Protocol
    The cells were fixed with 4% PFA (10min at room temperature)and then permeabilized with 20% PBST for 20 min at-20℃. The cells were then incubated in 5%BSA to block non-specific protein-protein interactions for 30 min at at room temperature .Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.

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    图标文献和实验
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      ,Tau22 小鼠促炎因子相关基因(Jun,Fas 和 Toll 样受体)和染色质重构相关基因(Hdac2)存在相互作用,提示在 Tau 蛋白病早期,神经胶质细胞存在炎症表型和表观遗传层面的调控。同时,Tau22 小鼠胶质细胞存在明显形态学异常。图片来源:nature为进一步验证 NLRP3 炎症小体参与 tau 蛋白病的机制,研究人员分别构建了人细胞凋亡相关斑点样蛋白 Pycard 敲除(Tau22 /Asc−/−)和 Cias1 敲除(Tau22 /Nlrp3−/−)小鼠。实验结果表明 Tau22

    • 肿瘤、感染、神经炎症…为啥都开始关注细胞焦亡?

      通路,诱导多种 NOD 样受体(例如 NLRP3)蛋白以及 pro-IL-1β/pro-IL-18 的表达;次级信号为活化信号,细胞内的 NOD 样受体在迅速识别危险相关分子模式或病原体相关分子模式(例如线粒体 DNA)后,与接头蛋白 ASC 组装,从而招募 pro-Caspase-1[4]。当 pro-Caspase-1 的局部浓度升高时,发生自体剪切,生成的片段 p20 和 p10 组成四聚体结构的具有生物活性的 Caspase-1(即活化的 Caspase-1)[5]。炎症小体通过调控

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