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MNDA (3C1) Rat mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2026年01月06日
  • W, 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

      MNDA (3C1) Rat mAb

    • 抗原

      nuclear extract from human granulocytes

    • 应用范围

      W, IF-IC, F

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 适应物种

      H

    • 供应商

      CST

    • 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  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
    W IF-IC F H Endogenous 50 Rat IgG1
    Protocols
    Specificity / Sensitivity

    MNDA (3C1) Rat mAb detects endogenous levels of total MNDA protein.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with nuclear extract from human granulocytes.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HL-60 and THP-1 cells using MNDA (3C1) Rat mAb.

    Flow Cytometry

    Flow Cytometry

    Flow cytometric analysis of Jurkat cells (red) and THP-1 cells (blue) using MNDA (3C1) Rat mAb.

    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of THP-1 cells (left) and Jurkat cells (right) using MNDA (3C1) Rat mAb (green). Actin filaments were labeled with DY-554 phalloidin (red).


    Background

    MNDA (myeloid cell nuclear differentiation antigen) is a transcription factor constitutively expressed in peripheral blood granulocytes and monocytes; low expression is also found in a subset of B cells (1,2). MNDA is a member of the interferon (IFN)-regulated 200 family of genes, which contain one or more copies of a partially conserved domain of 200 amino acid residues thought to mediate protein-protein interaction (3). MNDA may play a role in apoptosis and its expression is reduced in myelodysplastic syndromes (MDS) (4). MNDA has been proposed to be a marker for nodal marginal zone lymphoma (5).

    1. Briggs, R.C. et al. (1994) J Cell Biochem 56, 559-67.
    2. Miranda, R.N. et al. (1999) Hum Pathol 30, 1040-9.
    3. Landolfo, S. et al. (1998) Biochimie 80, 721-8.
    4. Briggs, R.C. et al. (2006) Cancer Res 66, 4645-51.
    5. Kanellis, G. et al. (2009) Leukemia 23, 1847-57.
    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
    • Immunofluorescent Staining of Mouse and Rat Leukocytes

      mAb. It is important to verify that no secondary reagent will bind the BD Fc Block™. Please see description in "The Uses of BD Fc Block™ in Immunophenotyping of Mouse and Rat Leukocytes". For very low-density cell surface markers (e.g.,cytokine

    • Notes on Making Rat x Y3 Monoclonal Antibody Producing Hybridomas

      Although Y3/Ag1.2.3 has its own myeloma light chain, their are numerous characteristics that make this a better parent line for making hybridomas than the 'Y0' chain loss variants or using NS0 to make rat x mouse hybrids. These are: a) Hybridomas

    • Dual- and Triple-Color Fluorospot

      in the analysis, e.g., IL-10, rat mAb 9D7 is used for coating and tag (different from FITC and biotin)-labeled rat mAb 12G8 is used for detection. All mAbs from Mabtech, Nacka Strand, Sweden. 4. Secondary reagents for amplification: Mouse anti-FITC mAb

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