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Mono-Methyl Arginine (Me-R4-10

0) Rabbit mAb
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  • 询价
  • Cell Signaling Technology已认证
  • 8015
  • USA
  • 2025年10月10日
  • W, IP, E-P
  • All
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Mono-Methyl Arginine (Me-R4-100) Rabbit mAb

    • 抗原

      synthetic peptide library containing mono-methyl arginine surrounded by degenerate amino acids

    • 应用范围

      W, IP, E-P

    • 级别

      详见MSDS文件

    • 供应商

      CST

    • 适应物种

      All

    • 保质期

      详见说明书

    • 库存

      大量

    • 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  E-P=ELISA (Peptide)
    Reactivity Key: All=All species expected
    Species cross-reactivity is determined by western blot.

    Applications Reactivity Sensitivity Isotype
    W IP E-P All Endogenous Rabbit IgG
    Protocols
    Specificity / Sensitivity

    Mono-Methyl Arginine (Me-R4 -100) Rabbit mAb recognizes endogenous levels of mono-methyl arginine protein. This is a general mono-methyl arginine motif antibody without sequence preferences. It does not cross-react with di-methyl arginine or unmethylated arginine.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide library containing mono-methyl arginine surrounded by degenerate amino acids. The antibody is formulated from four rabbit monoclones in order to cover a broad range of reactivity.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various mouse tissues using Mono-Methyl Arginine (Me-R4 -100) Rabbit mAb.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HCT 116 cells using Mono-Methyl Arginine (Me-R4 -100) Rabbit mAb. Specific signals are blocked by mono-methyl arginine antigen peptide, but not by non-methyl arginine control peptide.

    IP

    IP

    Immunoprecipitation of HCT 116 cell lysate using Mono-Methyl Arginine (Me-R4 -100) Rabbit mAb or Rabbit (DA1E) mAb IgG XP® Isotype Control #3900. Western blot detection was performed with Mono-Methyl Arginine (Me-R4 -100) Rabbit mAb. 10% input is shown in lane 1.


    Background

    Arginine methylation is a prevalent post-translational modification found on both nuclear and cytoplasmic proteins. Arginine methylated proteins are involved in many different cellular processes, including transcriptional regulation, signal transduction, RNA metabolism, and DNA damage repair (1-3). Arginine methylation is carried out by the arginine N-methyltransferase (PRMT) family of enzymes that catalyze the transfer of a methyl group from S-adenosylmethionine (AdoMet) to a guanidine nitrogen of arginine (4). There are three different types of arginine methylation: asymmetric dimethylarginine (aDMA, omega-NG,NG-dimethylarginine), where two methyl groups are placed on one of the terminal nitrogen atoms of the guanidine group of arginine; symmetric dimethylarginine (sDMA, omega-NG,N’G-dimethylarginine), where one methyl group is placed on each of the two terminal guanidine nitrogens of arginine; and monomethylarginine (MMA, omega-NG-dimethylarginine), where a single methyl group is placed on one of the terminal nitrogen atoms of arginine. Each of these modifications has potentially different functional consequences. Though all PRMT proteins catalyze the formation of MMA, Type I PRMTs (PRMT1, 3, 4, and 6) add an additional methyl group to produce aDMA, while Type II PRMTs (PRMT5 and 7) produce sDMA. Methylated arginine residues often reside in glycine-arginine rich (GAR) protein domains, such as RGG, RG, and RXR repeats (5). However, PRMT4/CARM1 and PRMT5 methylate arginine residues within proline-glycine-methionine rich (PGM) motifs (6).

    1. Bedford, M.T. and Richard, S. (2005) Mol Cell 18, 263-72.
    2. Pahlich, S. et al. (2006) Biochim Biophys Acta 1764, 1890-903.
    3. Bedford, M.T. and Clarke, S.G. (2009) Mol Cell 33, 1-13.
    4. McBride, A.E. and Silver, P.A. (2001) Cell 106, 5-8.
    5. Gary, J.D. and Clarke, S. (1998) Prog Nucleic Acid Res Mol Biol 61, 65-131.
    6. Cheng, D. et al. (2007) Mol Cell 25, 71-83.
    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
    • Protein arginine methylation

      Typical modification sites: RGG box or RXR sequence motifs R-arginine, G-glycine, X-any aminoacid. Enzymes catalysing protein arginine methylation: PRMT1 from rat and the human homologue HRMT1L2, human PRMT2 (HRMT1L1), rat and human PRMT

    • Technovit® 9100 Methyl Methacrylate

      in this leaflet. They are analogous to those used with methyl methacrylate (MMA) thin sections. Routine Staining Counterstaining of Sections for Immuno- and Enzyme-lmmunohistochemistry   Haematoxylin according to Mayer

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      :使用 Anti-phospho-Akt (Ser473) Rabbit mAb 对石蜡包埋的人乳腺癌组织进行免疫组织化学分析。(图 A)使用免疫组化试剂盒M&R HRP/DAB Detection IHC Kit,抗体 1:100 稀释;(图 B) 采用普通免疫组化试剂盒,抗体 1:25 稀释。 图 6 免疫组化实验检测 Erk1/2 表达 注:使用 Anti-Erk1/2 Mouse mAb与p44/42 MAPK (Erk1/2)Rabbit mAb 对正常小鼠心脏组织进行免疫

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