FLIP凋亡调节基因之一抗体产品图

FLIP凋亡调节基因之一抗体

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  • ¥1380
  • 美国santa
  • 美国
  • YS-1120R
  • 2026年05月21日
  • WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 IF=1:100-500
  • Rabbit
  • 详情请来电索取说明书
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 免疫原

      KLH conjugated

    • 亚型

      IgG

    • 形态

      冻干粉

    • 保存条件

      负20°保存

    • 克隆性

      多克隆

    • 标记物

      详情请来电索取说明书

    • 适应物种

      详情请来电索取说明书

    • 宿主

      Rabbit

    • 应用范围

      WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 IF=1:100-500

    • 浓度

      1mg/ml

    • 靶点

      详情请来电索取说明书

    • 抗体英文名

      FLIP

    • 抗体名

      凋亡调节基因之一抗体

    • 规格

      100ul

    英文名称FLIP
    中文名称凋亡调节基因之一抗体
    别    名CASP8 and FADD-like apoptosis regulator subunit p43; CASP8 and FADD-like apoptosis regulator subunit p43; Flice-like Inhibitory protein; c FLIP; c FLIPL; c FLIPR; c FLIPS; c-FLIP; CASH; CASP8 and FADD like apoptosis regulator; CASP8 and FADD like apoptosis regulator precursor; CASP8AP1; Caspase Eight Related Protein; Caspase homolog; Caspase Homologue; Caspase Like Apoptosis Regulatory Protein; Caspase related inducer of apoptosis; CASPER; Cellular FLICE like inhibitory protein; CFLA; CFLAR; CLARP; FADD like anti apoptotic molecule; FADD Like Anti-apoptotic Molecule 1; FADD-like antiapoptotic molecule 1; FADD like antiapoptotic molecule 1; FADD Like Apoptosis Regulator; FLAME 1; FLAME; FLAME1; FLAME-1; FLICE Inhibitor Protein; FLIP; FLIPs; I FLICE; I-FLICE; Inhibitor of FLICE; Inhibitor of FLICE; MACH Related Inducer of Toxicity; MACH-related inducer of toxicity; mFLIP; MRIT; USURPIN; Usurpin beta; FLICE-like inhibitory protein short form; FLICE-like inhibitory protein long form; CFLAR_HUMAN; Cellular FLICE-like inhibitory protein.  
    规格价格50ul  100ul  200ul
    研究领域肿瘤  细胞生物  信号转导  细胞凋亡  
    抗体来源Rabbit
    克隆类型Polyclonal
    交叉反应 Human, Mouse, Rat, Dog, Pig, Cow, 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=3ug/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43/52kDa
    细胞定位细胞浆 
    性    状Lyophilized or Liquid
    浓    度1mg/ml
    免 疫 原KLH conjugated synthetic peptide derived from human CASP8 and FADD-like apoptosis regulator subunit p43:7-100/480 
    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.
    PubMedPubMed
    产品介绍background:
    The protein encoded by this gene is a regulator of apoptosis and is structurally similar to caspase-8. However, the encoded protein lacks caspase activity and appears to be itself cleaved into two peptides by caspase-8. Several transcript variants encoding different isoforms have been found for this gene, and partial evidence for several more variants exists. [provided by RefSeq, Feb 2011]

    Function:
    Apoptosis regulator protein which may function as a crucial link between cell survival and cell death pathways in mammalian cells. Acts as an inhibitor of TNFRSF6 mediated apoptosis. A proteolytic fragment (p43) is likely retained in the death-inducing signaling complex (DISC) thereby blocking further recruitment and processing of caspase-8 at the complex. Full length and shorter isoforms have been shown either to induce apoptosis or to reduce TNFRSF-triggered apoptosis. Lacks enzymatic (caspase) activity.

    Subunit:
    TNFRSF6 stimulation triggers recruitment to the death-inducing signaling complex (DISC) formed by TNFRSF6, FADD and caspase-8. A proteolytic fragment (p43) stays associated with the DISC. Also interacts with caspase-10, caspase-3, TRAF1, TRAF2 and Bcl-X(L) (in vitro). Interacts with HBV protein X.

    Tissue Specificity:
    Widely expressed. Higher expression in skeletal muscle, pancreas, heart, kidney, placenta, and peripheral blood leukocytes. Also detected in diverse cell lines. Isoform 8 is predominantly expressed in testis and skeletal muscle.

    Post-translational modifications:
    Proteolytically processed; probably by caspase-8. Processing likely occurs at the DISC and generates subunit p43 and p12.

    Similarity:
    Belongs to the peptidase C14A family. 
    Contains 2 DED (death effector) domains.

    SWISS:
    O15519

    Gene ID:
    8837

    Database links:
    Entrez Gene: 8837 Human
    Entrez Gene: 12633 Mouse
    Entrez Gene: 117279 Rat
    Omim: 603599 Human
    SwissProt: O15519 Human
    SwissProt: O35732 Mouse
    Unigene: 390736 Human
    Unigene: 336848 Mouse


    Important Note:
    This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 

    FLIP参与凋亡的调节。此抗体在长型和短型的FLIP异构体中均表达。短型FLIP包含2个死亡效应基因结构区,同源于FAS相关蛋白死亡效应基因结构区。长型FLIP包含1个附加的Caspase 样结构区,但是他缺少一个催化部位和在大多数Caspase 蛋白中形成底物结合束的残基。
    产品图片 产品细节图片1
    Sample: 
    Hela(Human) Cell Lysate at 30 ug
    Primary: Anti-FLIP (bs-0119R) at 1/500 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 43/52 kD
    Observed band size: 52 kD

    产品细节图片2
    Sample: 
    Pancreas (Mouse) Lysate at 40 ug
    Primary: Anti-FLIP (bs-0119R) at 1/500 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 43/52 kD
    Observed band size: 43/52 kD

    产品细节图片3
    Sample: 
    Muscle(Mouse) Lysate at 40 ug
    Primary:Anti-FLIP (bs-0119R) at 1/2000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 43/52 kD
    Observed band size: 43 kD

    产品细节图片4
    Sample: 
    Muscle(Mouse) Lysate at 40 ug
    Primary: Anti-FLIP (bs-0119R) at 1/500 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 43/52 kD
    Observed band size: 43 kD

    产品细节图片5
    Paraformaldehyde-fixed, paraffin embedded (rat liver 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 (FLIP) Polyclonal Antibody, Unconjugated (bs-0199R) at 1:400 overnight at 4°C, followed by a conjugated secondary (sp-0023) for 20 minutes and DAB staining.

    Tissue/cell: rat brain 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-FLIP/c FLIP Polyclonal Antibody, Unconjugated(bs-0119R) 1:300, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining

    产品细节图片6
    Blank control (Black line): HUVEC (Black). 
    Primary Antibody (green line): Rabbit Anti-FLIP antibody (bs-0119R) 
    Dilution: 1μg /10^6 cells; 
    Isotype Control Antibody (orange line): Rabbit IgG .
    Secondary Antibody (white blue line): Goat anti-rabbit IgG-AF647
    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 room temperature. The cells were then incubated in 5%BSA to block non-specific protein-protein interactions for 30 min 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
    相关实验
    • 【求助】请问western blot做凋亡检测时,识别caspase-3酶原和激活的caspase-3的抗体是相同的吗?

      lsdcfhyj 以及检测PARP的裂解前后蛋白水平用的抗体是否都是一样的? edwardellen 有两者都识别的,也有专门识别剪切体不识别酶原的,用过cell signal的,两种都很好用。 PARP也有可以同时识别全长和剪切体的抗体。 magichunter 检测caspase-3和激活型的caspase-3分别需要两种不同的抗体,一般CST公司卖的分别包括:cleaved

    • 嵌合抗CD20Fab’抗体片段诱导Raji 细胞的凋亡机制

      【摘要】目的探讨嵌合抗CD20抗体Fab’片段的抗肿瘤机制。方法应用MTT法检测Fab’片段对Raji细胞生长的抑制作用,用Annexin V-FITC和PI测定Fab’片段对Raji细胞凋亡的诱导作用,用RT-PCR和Western blot检测Raji细胞中bcl-2表达的变化。结果嵌合抗CD20Fab’片段对Raji细胞具有明显的抑制作用IC50值为24.2 µg/ml,并呈剂量依赖性;嵌合抗CD20Fab’片段能诱导Raji细胞的凋亡,并降低Raji细胞中bcl-2基因及其蛋白的表达

    • 单链抗体可变区基因片段五聚体作用于凋亡诱导配体受体-2来增强其对癌症的治疗作用

      一种有效的途径来延长它在血中的半衰期。这里有好几种方法可以用来生成多聚的scFvs。例如,两个或更多的scFvs已经通过改变重链可变区和轻链可变区的连接肽的长度被组合成二聚体或三聚体,并且多个scFv分子已经通过化学交联被结合在了一起,例如聚乙二醇化。此外,scFvs的多聚体已经通过与多聚的结构域相结合而被合成,这些结构域包括Fc、亮氨酸拉链结构等。最近的一篇论文指出scFv-Fc-scFv双特异性分子可以导致半衰期约460h的抗体样清除。作为一个参与细胞凋亡的关键分子,肿瘤坏死因子相关凋亡

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