CD171/L1CAM Recombinant Rabbit mAb, Cy3 conjugated(bsm-52926R-Cy3)-100ul

CD171/L1CAM Recombinant Rabbit

mAb, Cy3 conjugated(bsm-52926R-Cy3)-100ul
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  • ¥2980
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  • bsm-52926R-Cy3
  • 2025年12月01日
  • 产品信息以Bioss网站为准
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      100ul

    产品编号bsm-52926R-Cy3
    英文名称CD171/L1CAM Recombinant Rabbit mAb, Cy3 conjugated
    中文名称Cy3标记的神经细胞粘附分子配体1重组兔单抗
    英文别名L1CAM_HUMAN; Neural cell adhesion molecule L1; CAML1; MIC5; N-CAM-L1; NCAM-L1; CD171; L1 cell adhesion molecule; S10; HSAS; MASA; SPG1; HSAS1; N-CAM-L1;
    产品应用IF=1:200-800

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

    抗体来源Rabbit
    免疫原A synthesized peptide derived from human NCAM L1
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Recombinant
    浓度1mg/ml
    储存液1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.02% Proclin300.
    研究领域

    Neuroscience > Neurology process > Growth and Development > Axonal Guidance Proteins

    Neuroscience > Neurology process > Neurogenesis

    Signal Transduction > Cytoskeleton / ECM > Cell Adhesion > Cell Adhesion Molecules > Liver

    亚细胞定位Cell membrane; Single-pass type I membrane protein.
    相似性Belongs to the immunoglobulin superfamily. L1/neurofascin/NgCAM family.
    Contains 5 fibronectin type-III domains.
    Contains 6 Ig-like C2-type (immunoglobulin-like) domains.
    功能Cell adhesion molecule with an important role in the development of the nervous system. Involved in neuron-neuron adhesion, neurite fasciculation, outgrowth of neurites, etc. Binds to axonin on neurons.
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料L1cam (L1 cell adhesion molecule isoform 1 precursor) is an axonal glycoprotein belonging to the immunoglobulin supergene family. The ectodomain, consisting of several immunoglobulin-like domains and fibronectin-like repeats (type III), is linked via a single transmembrane sequence to a conserved cytoplasmic domain. This cell adhesion molecule plays an important role in nervous system development, including neuronal migration and differentiation. Mutations in the gene cause three X-linked neurological syndromes known by the acronym CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus). Alternative splicing of a neuron-specific exon is thought to be functionally relevant. [provided by RefSeq].

     

    应用推荐稀释比例
    {IF}{1:200-800}

     

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