Msx1 (G116) Antibody

Msx1 (G116) Antibody

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  • Cell Signaling Technology已认证
  • USA
  • 2025年11月06日
  • W
  • Rabbit
  • H
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    • 详细信息
    • 技术资料
    • 抗体英文名

      Msx1 (G116) Antibody

    • 抗原

      synthetic peptide corresponding to amino acid sequence surrounding Gly116 of human Msx1 protein

    • 应用范围

      W

    • 宿主

      Rabbit

    • 适应物种

      H

    • 库存

      大量

    • 保质期

      详见说明书

    • 供应商

      CST

    • 级别

      详见MSDS文件

    • 是否单克隆

      2

    • 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
    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) Source
    W H Endogenous 32 Rabbit
    Protocols
    Specificity / Sensitivity

    Msx1 (G116) Antibody detects endogenous levels of total Msx1 protein.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to amino acid sequence surrounding Gly116 of human Msx1 protein. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HCT 116 and SW480 cells using Msx1 (G116) Antibody.

    Background

    Msh homeobox 1 (Msx1) is a Muscle Segment Homeobox (Msh) gene family member that acts as a transcriptional repressor during embryonic development, playing an important role in limb pattern formation, craniofacial development, and tooth development (1-3). Msx1 is expressed in the mesenchyme of the developing nail bed (2) and in fetal hair follicles, epidermis and fibroblasts; reduced expression is seen in adult epithelial-derived tissues (4). Msx1 acts in concert with the Wnt1 network to establish the midbrain dopaminergic progenator domain, a region that gives rise to neurons that are critical for normal brain function and are the cells affected in Parkinson disease (5). Mutation in the corresponding Msx1 gene correlates with abnormal tooth development in patients diagnosed with Wolf-Hirschhorn syndrome (6). Other genetic changes in the Msx1 gene result in Witkop Syndrome ("tooth and nail syndrome") and cases of abnormal tooth development associated with non-syndromic orofacial clefting (2,7).

    1. Jezewski, P.A. et al. (2003) J Med Genet 40, 399-407.
    2. Jumlongras, D. et al. (2001) Am J Hum Genet 69, 67-74.
    3. Lidral, A.C. and Reising, B.C. (2002) J Dent Res 81, 274-8.
    4. Stelnicki, E.J. et al. (1997) Differentiation 62, 33-41.
    5. Andersson, E. et al. (2006) Cell 124, 393-405.
    6. Nieminen, P. et al. (2003) J Dent Res 82, 1013-7.
    7. van den Boogaard, M.J. et al. (2000) Nat Genet 24, 342-3.
    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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