MKL2 Rabbit pAb, BF488 conjugated(bs-18948R-BF488)-100ul

MKL2 Rabbit pAb, BF488 conjuga

ted(bs-18948R-BF488)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-18948R-BF488
  • 2025年09月30日
  • 产品信息以Bioss网站为准
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      100ul

    产品编号bs-18948R-BF488
    英文名称MKL2 Rabbit pAb, BF488 conjugated
    中文名称BF488标记的巨核细胞白血病2抗体
    英文别名FLJ31823; Megakaryoblastic leukemia 2; megakaryoblastic leukemia 2 protein; MKL/myocardin-like 2; MKL/myocardin-like protein 2; Mkl2; MKL2_HUMAN; MRTF-B; Myocardin-related transcription factor B; NPD001.MKS.
    产品应用ICC/IF=1:50-200, IF=1:100-500

    Not yet tested in other applications.
    Optimal working dilutions must be determined by the end user.

    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from human MKKS
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    浓度1mg/ml
    储存液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    研究领域

    Cardiovascular > Heart > Cardiogenesis > Transcription factors/regulators

    Epigenetics and Nuclear Signaling > Transcription > Co-factors

    Epigenetics and Nuclear Signaling > Transcription > Other factors

    Epigenetics and Nuclear Signaling > Transcription > Transcription Factors

    Stem Cells > Mesenchymal Stem Cells > Myogenesis

    亚基Interacts with MKL1 and SRF.
    亚细胞定位Nucleus.
    组织特异性Widely expressed in adult and fetal tissues.
    相似性Belongs to the TCP-1 chaperonin family.
    功能Acts as a transcriptional coactivator of serum response factor (SRF). Required for skeletal myogenic differentiation.
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料This gene encodes a protein which shares sequence similarity with other members of the type II chaperonin family. The encoded protein is a centrosome-shuttling protein and plays an important role in cytokinesis. This protein also interacts with other type II chaperonin members to form a complex known as the BBSome, which involves ciliary membrane biogenesis. This protein is encoded by a downstream open reading frame (dORF). Several upstream open reading frames (uORFs) have been identified, which repress the translation of the dORF, and two of which can encode small mitochondrial membrane proteins. Mutations in this gene have been observed in patients with Bardet-Biedl syndrome type 6, also known as McKusick-Kaufman syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]

     

    应用推荐稀释比例
    {ICC/IF}{1:50-200}
    {IF}{1:100-500}

     

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