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Met (L6E7) Mouse mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年12月18日
  • IF-IC, F
  • H
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Met (L6E7) Mouse mAb

    • 抗原

      mammalian cells expressing an amino terminal fragment of c-Met protein

    • 应用范围

      IF-IC, F

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 保质期

      详见说明书

    • 适应物种

      H

    • 供应商

      CST

    • 是否单克隆

      1

    • 保存条件

      -20°c

    • 规格

      100 ul (200 tests)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (200 tests)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:  IF-IC=Immunofluorescence (Immunocytochemistry)  F=Flow Cytometry
    Reactivity Key:  H=Human
    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
    IF-IC F H Endogenous 145 Mouse IgG3
    Protocols

    * Product-specific protocol.

    Specificity / Sensitivity

    Met (L6E7) Mouse mAb recognizes endogenous levels of total Met protein.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with mammalian cells expressing an amino terminal fragment of c-Met protein.

    Flow Cytometry

    Flow Cytometry

    Flow cytometric analysis of unpermeabilized Ramos (red), T-47D (blue), HCT 116 (orange), and MKN-45 (green) cells using Met (L6E7) Mouse mAb.

    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of HCT 116 (left) and T-47D (right) cells using MET (L6E7) Mouse mAb (green). Actin filaments were labeled with DY-554 phalloidin (red). Blue pseudocolor = DRAQ5® #4084 (fluorescent DNA dye).

    Background

    Met, a high affinity tyrosine kinase receptor for hepatocyte growth factor (HGF, also known as scatter factor) is a disulfide-linked heterodimer made of 45 kDa α- and 145 kDa β-subunits (1,2). The α-subunit and the amino-terminal region of the β-subunit form the extracellular domain. The remainder of the β-chain spans the plasma membrane and contains a cytoplasmic region with tyrosine kinase activity. Interaction of Met with HGF results in autophosphorylation at multiple tyrosines, which recruit several downstream signaling components, including Gab1, c-Cbl, and PI3 kinase (3). These fundamental events are important for all of the biological functions involving Met kinase activity. The addition of a phosphate at cytoplasmic Tyr1003 is essential for Met protein ubiquitination and degradation (4). Phosphorylation at Tyr1234/1235 in the Met kinase domain is critical for kinase activation. Phosphorylation at Tyr1349 in the Met cytoplasmic domain provides a direct binding site for Gab1 (5). Research studies have shown that altered Met levels and/or tyrosine kinase activities are found in several types of tumors, including renal, colon, and breast. Thus, investigators have concluded that Met is an attractive potential cancer therapeutic and diagnostic target (6,7).

    1. Cooper, C.S. et al. (1984) Nature 311, 29-33.
    2. Bottaro, D.P. et al. (1991) Science 251, 802-4.
    3. Bardelli, A. et al. (1997) Oncogene 15, 3103-11.
    4. Taher, T.E. et al. (2002) J Immunol 169, 3793-800.
    5. Schaeper, U. et al. (2000) J Cell Biol 149, 1419-32.
    6. Eder, J.P. et al. (2009) Clin Cancer Res 15, 2207-14.
    7. Sattler, M. and Salgia, R. (2009) Update Cancer Ther 3, 109-118.
    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
    • Purification of mAb (IgG)

      (adjust pH to 7.8 with Binding buffer; red color) to the Protein A column.Mouse antibodies of the IgG1 subclass do not have a high affinity for protein A. Purification on protein A beads using standard conditions will yield approximately 1/10

    • Purification of mAb (IgG)

        Purification of mAb (IgG) by Chang-Duk Jun, 03/14/2000 Purpose Materials Antibody 7E3 , 2L sup grown in flasks, frozen and thawed overnight. BioRad Affi-Gel Protein A MAPS II Buffers

    • T-Cell Activation Using mAb to CD3

      One of the most common ways to assess T cell activation is to measure T cell proliferation upon in vitro stimulation of T cells via antigen or agonistic antibodies to TCR. This protocol is written as a starting point for examining in vitro proliferation of mouse

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