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Cox1 (D2G6) Rabbit mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年07月14日
  • W, IP
  • H,M
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Cox1 (D2G6) Rabbit mAb

    • 抗原

      synthetic peptide corresponding to residues surrounding Ile123 of human Cox1 protein

    • 应用范围

      W, IP

    • 供应商

      CST

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 适应物种

      H,M

    • 保质期

      详见说明书

    • 是否单克隆

      1

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting  IP=Immunoprecipitation
    Reactivity Key:  H=Human  M=Mouse
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Isotype
    W IP H M Endogenous 70 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    Cox1 (D2G6) Rabbit mAb recognizes endogenous levels of glycosylated Cox1 protein; it also weakly recognizes unglycosylated Cox1 protein.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ile123 of human Cox1 protein.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from C2C12 and HeLa cells using Cox1 (D2G6) Rabbit mAb.

    Background

    Cyclooxygenase1 (Cox1) and cyclooxygenase2 (Cox2), family members with 60% homology in humans, catalyze prostaglandin production from arachidonic acid (1,2). While Cox1 expression is constitutive in most tissues, Cox2 expression is induced by lipopolysaccharide (LPS) and peptidoglycan (PGN) (3). PGN activates Ras, leading to phosphorylation of Raf at Ser338 and Erk1/2 at Tyr204. The activation of MAP kinase signaling results in subsequent activation of IKKα/β, phosphorylation of IκBα at Ser32/36, and NF-κB activation. Finally, activation of the transcription factor NF-κB is responsible for the induction of Cox2 expression (4). LPS and PGN induce the clinical manifestations of arthritis and bacterial infections, such as inflammation, fever, and septic shock (5), making Cox2 a useful target for therapeutic anti-inflammatory drugs (3). Cox1 and Cox2 also play a role in the neuropathology of Alzheimer's disease by potentiating γ-secretase activity and β-amyloid generation (6).

    1. Xie, W.L. et al. (1991) Proc Natl Acad Sci USA 88, 2692-6.
    2. Vane, J.R. et al. (1998) Annu Rev Pharmacol Toxicol 38, 97-120.
    3. O'Neill, G.P. et al. (1994) Mol Pharmacol 45, 245-54.
    4. Chen, B.C. et al. (2004) J Biol Chem 279, 20889-97.
    5. Wang, Q. et al. (2001) Infect Immun 69, 2270-6.
    6. Qin, W. et al. (2003) J Biol Chem 278, 50970-7.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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    图标文献和实验
    相关实验
    • Methods for the Detection of D-Amino-Acid Oxidase

      then twice for 5 min. It was incubated for 1 hr in TBS-T containing rabbit anti-hog D-amino-acid oxidase IgG (1/3,000 dilution) and quickly rinsed twice with TBS-T and further washed in TBS-T once for 15 min then twice for 5 min. The membrane was incubated

    • 组化染色背景高?没信号?一篇文章带你快速掌握免疫组化!

      组织化学分析。(图 C)使用Anti-Erk1/2 Mouse mAb 鼠单抗进行目的蛋白检测;(图 D) 使用p44/42 MAPK (Erk1/2)Rabbit mAb 兔单抗进行目的蛋白检测。 图 7 免疫组化实验检测Akt表达 注:使用 Anti-Akt (pan) Rabbit mAb 对正常小鼠肝组织进行免疫组织化学分析。(图 E)使用免疫组化试剂盒 M&R HRP/DAB Detection IHC Kit,抗体1:100 稀释;(图F)使用另一种试剂盒,抗体 1:100 稀释。

    • Methods for the Detection of D-Amino-Acid Oxidase

      min then twice for 5 min. It was incubated for 1 hr in TBS-T containing rabbit anti-hog D-amino-acid oxidase IgG (1/3,000 dilution) and quickly rinsed twice with TBS-T and further washed in TBS-T once for 15 min then twice for 5 min. The membrane

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