<legend id="oozfl"></legend>
    <strike id="oozfl"></strike>
    掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
      
    客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯系我們
    產品中心-北京博奧森生物技術有限公司
    首頁 > 產品中心 > 一抗 > 產品信息
    GOLPH3 Rabbit pAb (bs-13488R)  
    訂購熱線:400-901-9800
    訂購郵箱:sales@bioss.com.cn
    訂購QQ:  400-901-9800
    技術支持:techsupport@bioss.com.cn
    50ul/1180.00元
    100ul/1980.00元
    200ul/2800.00元
    大包裝/詢價

    產品編號 bs-13488R
    英文名稱 GOLPH3 Rabbit pAb
    中文名稱 高爾基體磷蛋白3抗體
    別    名 Coat protein GPP34; FLJ90675; Golgi peripheral membrane protein 1, 34 kDa; Golgi phosphoprotein 3(coat protein); Golgi phosphoprotein 3; GOLP3_HUMAN; Golph3; GPP34; MIDAS; Mitochondrial DNA absence factor.  
    研究領域 腫瘤  細胞生物  信號轉導  細胞類型標志物  細胞膜蛋白  
    抗體來源 Rabbit
    克隆類型 Polyclonal
    克 隆 號
    交叉反應 Human (predicted: Mouse,Rat,Cow,Chicken,Dog,Horse)
    產品應用 WB=1:500-2000
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    理論分子量 34 kDa
    檢測分子量
    細胞定位 細胞漿 細胞膜 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human GOLPH3: 51-150/298 
    亞    型 IgG
    純化方法 affinity purified by Protein A
    緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    PubMed PubMed
    產品介紹 The Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. GOLPH3L (golgi phosphoprotein 3-like), also known as GPP34R, is a 285 amino acid cytoplasmic protein that localizes to the Golgi apparatus. Belonging to the GOLPH3/VPS74 family, GOLPH3L may have a regulatory role in Golgi trafficking. GOLPH3L is encoded by a gene located on human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

    Function:
    Involved in modulation of mTOR signaling. Involved in the regulation of mitochondrial lipids, leading to increase of mitochondrial mass. Potential oncogene.

    Subunit:
    Homodimer. Interacts with VPS35.

    Subcellular Location:
    Cell membrane. Endosome. Cytoplasm. Golgi apparatus > Golgi stack membrane. Mitochondrion intermembrane space.

    Tissue Specificity:
    Detected in muscle fibers of patients with mitochondrial diseases; not detected in normal muscle fibers.

    Post-translational modifications:
    Phosphorylated.

    Similarity:
    Belongs to the GOLPH3/VPS74 family.

    SWISS:
    Q9H4A6

    Gene ID:
    64083

    Database links:

    Entrez Gene: 64083 Human

    Entrez Gene: 531359 Cow

    Entrez Gene: 66629 Mouse

    Entrez Gene: 78961 Rat

    Omim: 612207 Human

    SwissProt: Q9H4A6 Human

    SwissProt: Q9CRA5 Mouse

    SwissProt: Q9ERE4 Rat

    Unigene: 408909 Human

    Unigene: 250936 Mouse

    Unigene: 64519 Rat



    產品圖片
    Sample: Hela(Human) Cell Lysate at 30 ug Primary: Anti- GOLPH3 (bs-13488R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 34 kD Observed band size: 33 kD
    版權所有 2004-2026 www.radiasunchina.com 北京博奧森生物技術有限公司
    通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
    通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
    京ICP備05066980號-1         京公網安備110107000727號
    国产剧情演绎系列丝袜高跟|一级毛片av性爱黄色网站|欧美三级午夜理伦三级|国产av巨作情欲放纵|亚洲 欧美 中文 日韩aⅴ

    <legend id="oozfl"></legend>
    <strike id="oozfl"></strike>