CRLF3 Rabbit pAb, BF700 conjugated(bs-14062R-BF700)-100ul

CRLF3 Rabbit pAb, BF700 conjug

ated(bs-14062R-BF700)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-14062R-BF700
  • 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-14062R-BF700
    英文名称CRLF3 Rabbit pAb, BF700 conjugated
    中文名称BF700标记的细胞因子受体样因子3抗体
    英文别名CREME 9; CREME9; CRLF 3; CRLM9; Cytokine receptor like factor 3; Cytokine receptor like molecule 9; Cytokine receptor related protein 4; CYTOR4; FRWS; MGC20661; P48; p48.2; Type I cytokine receptor like factor; Type I cytokine receptor like factor p48; CRLF3_HUMAN.
    产品应用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 CRLF3
    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

    Immunology > Innate Immunity > Cytokines

    亚细胞定位Cytoplasmic
    组织特异性Expressed in several embryonic and adult tissues, including adult and fetal brain, liver, spleen and pancreas. Expressed in adult, but not fetal kidney. Expressed in skin and squamous cell carcinoma (SCC) and in several other cancer types. Also detected in lesion actinic keratosis (AK).
    相似性Belongs to the cytokine receptor-like factor 3 family.
    Contains 1 fibronectin type-III domain._x000D_
    功能CRLF3 (Cytokine receptor-like factor 3) contains one fibronectin type-III domain. It is expressed in skin and squamous cell carcinoma (SCC) and in lesion actinic keratosis (AK).
    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 cytokine receptor-like factor that may negatively regulate cell cycle progression at the G0/G1 phase. Studies of the related rat protein suggest that it may regulate neuronal morphology and synaptic vesicle biogenesis. This gene is one of several genes located in the neurofibromatosis type I tumor suppressor region on the q arm of chromosome 17, a region that is subject to microdeletions, duplications, chromosomal breaks and rearrangements. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 2 and 5. [provided by RefSeq, Aug 2012]

     

    应用推荐稀释比例
    {IF}{1:100-500}

     

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