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Rabbit Anti-Myc tag agarose beads

价格 2,824.00 供应商现货 : 3-5个工作日
货号 S0B1642
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产品规格
  • 宿主来源

    Rabbit
  • 免疫原

    Recombinant Protein
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 纯化方式

    Protein A
  • 标记

    Agarose beads
  • 性状

    Liquid
  • 缓冲体系

    50% slurry in PBS pH7.4, 0.05% Proclin 300. Ensure thorough mixing before each use. Wide-mouth pipette tips are recommended. In case of difficulty in aspiration due to improper operation, additional Storage Buffer can be added at your discretion.
  • 储存条件

    12 months from date of receipt / reconstitution, 2 to 8 °C as supplied

  • 应用

背景介绍
  • The c-Myc is a polypeptide protein tag derived from the c-myc gene product, which can be added to the protein by recombinant DNA technology. It contains 10 amino acids (EQKLISEEDL) with a molecular weight of 1.2 KDa and can be fused to the N-terminus or C-terminus of the target protein for purification and detection. The Myc tag is widely used in various expression systems, including bacteria, yeast, insects and mammalian cells, to detect the expression of fusion proteins. It can be used for affinity chromatography and purified by coupling the Myc-tagged antibody to divinylsulfone-activated agarose.

  • 电泳

    • Rabbit Anti-Myc tag agarose Beads were used to immunoprecipitate 2 x Myc tag-mouse IgE-His tag from Expi293F system.
      During elution with Pepide elution buffer, the enriched Myc fusion protein are released from the agarose beads.
      SDS-PAGE analysis was performed.
      Lane 1: Input
      Lane 2: Flow-through
      Lane 3: 2 x Myc tag-mouse IgE-His tag protein.

    • Rabbit Anti-Myc tag agarose Beads were used to immunoprecipitate 2 x Myc tag-mouse IgE-His tag from Expi293F system.
      During elution with Pepide elution buffer, the enriched Myc fusion protein are released from the agarose beads.
      SDS-PAGE analysis was performed.
      Lane 1: Input
      Lane 2: Flow-through
      Lane 3: 2xMyc tag-mouse IgE-His tag protein.

  • ChIP

    • Chromatin immunoprecipitation (ChIP) was performed on 293F cells were either untransfected (left panel) or transfected with an MYC-tagged human H3 construct (right panel) cross - linked with 1% formaldehyde for 10 min, then chromatin was fragmented by sonication. Parallel reactions used Rabbit Anti-Myc tag agarose beads, H3 beads and Rabbit lgG lsotype Control agarose beads for immunoprecipitation.
      Post-immunoprecipitation, both samples were washed, eluted, and cross - links reversed. Purified DNA was analyzed by qPCR.
      qPCR (%input: immunoprecipitated DNA/input DNA) showed the enrichment of RPL30, MYOD1 and SAT-α in Rabbit Anti-Myc tag agarose beads-immunoprecipitated sample.

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