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MORN4/C10orf83 Rabbit pAb(bs-1

7721R)-50ul/100ul/200ul
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  • ¥1180 - 2800
  • Bioss已认证
  • bs-17721R
  • 2025年10月24日
  • 产品信息以Bioss网站为准
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    • 规格

      50ul/100ul/200ul

    规格:50ul产品价格:¥1180.0
    规格:100ul产品价格:¥1980.0
    规格:200ul产品价格:¥2800.0
    产品编号bs-17721R
    英文名称MORN4/C10orf83 Rabbit pAb
    中文名称10号染色体开放阅读框83抗体
    英文别名44050 protein; C10orf83; Chromosome 10 open reading frame 83; MORN repeat containing 4; MORN repeat-containing protein 4; Morn4; MORN4_HUMAN; Protein 44050; Retinophilin.
    产品应用IHC-P=1:100-500, IHC-F=1:100-500, IF=1:100-500

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

    交叉反应Mouse (Human, Rat, Dog, Cow, Horse)
    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from human MORN4/C10orf83
    亚型IgG
    性状Liquid
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    理论分子量16 kDa
    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

    Signal Transduction > Cytoskeleton / ECM > Cytoskeleton > Microtubules > MT Associated Proteins > MARK

    Signal Transduction > Protein Phosphorylation > Ser / Thr Kinases > Other Kinases

    相似性Contains 4 MORN repeats.
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料MORN4 is a 146 amino acid protein that contains four MORN repeats and exists as two alternatively spliced isoforms. The gene encoding MORN4 maps to human chromosome 10, which contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious.

     

    应用推荐稀释比例
    {IHC-P}{1:100-500}
    {IHC-F}{1:100-500}
    {IF}{1:100-500}

     

    产品细节图片1
    P‌‌araformaldehyde-fixed, paraffin embedded (Mouse brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (MORN4) Polyclonal Antibody, Unconjugated (bs-17721R) at 1:500 overnight at 4°C, followed by a conjugated secondary (sp-0023) for 20 minutes and DAB staining.

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    图标文献和实验
    相关实验
    • Immunity:北大蒋争凡课题组发现 STING 后高尔基体囊泡转运的重要性及机制

      )及维持 STING 激活所需要的脂膜环境(lipid environment),从而帮助 STING 更加稳定高效的激活。 本工作首先通过 CRISPR-Cas9 介导的全基因组筛选在 HeLa 细胞系中鉴定到一个未知功能的新基因 C10ORF76  (又名 ARMH3)  对 STING 的激活十分重要。ARMH3 是一个鲜少被研究的蛋白,为数不多的几篇文章暗示了它对于 PI4KB 发挥激酶活性来磷酸化磷脂酰肌醇(phosphatidylinositol,PI)生成 PI4P 十分重要。免疫

    • Immunochemical Detection of a Fluorophore Derived from the Lipid Peroxidation Product 4-Hydroxy-2-Nonenal and Lysine

      = NAL), appears to form upon oxidative cyclization of the nonfluorescent 2:1 lysine-HNE Michael adduct-Schiff base cross-link (Scheme 1). Polyclonal antibody (PAb) to the NAL-HNE fluorophore was raised in rabbit and found to be highly specific

    • 【求助】蛋白激酶C的信号通路

      3BPAkNHeZbAxoknWOPsDS0sDPy3eI6wn0x9tcLz64SWbSH3bJmGW0SOuqItUeSEJZOqnryFHRC9Y3/s83LSUtca28w5545HEtWDLcZh12uP36kSXWs6PLnn76acsWWu2mW+6yb3zrm3bs0ZNt7ty59g9/93UR87Sdfs659vyLL9tQ5bthwxpbsWql1WQi8m+33G4/vOon9o6zTlff6rX7H1gsrx0t9r2rf2JXX3+jffETH7efXX+tXfKej9t1133fvvf9q/x+XPjzm60

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