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FUNDC1 Rabbit pAb(bs-13227R)-5

0ul/100ul
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  • ¥1180 - 1980
  • Bioss已认证
  • bs-13227R
  • 2025年10月16日
  • 产品信息以Bioss网站为准
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      50ul/100ul

    规格:50ul产品价格:¥1180.0
    规格:100ul产品价格:¥1980.0
    产品编号bs-13227R
    英文名称FUNDC1 Rabbit pAb
    中文名称X三体综合症相关蛋白FUNDC1抗体
    英文别名FUN14 domain containing protein 1; FUN14 domain-containing protein 1; FUND1_HUMAN.
    产品应用WB=1:300-800

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

    交叉反应Human, Mouse, Rat
    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from mouse FUNDC1
    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17 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

    Cell Biology > Other Antibodies > Other Antibodies

    亚基Interacts (via YXXL motif) with MAP1 LC3 family proteins MAP1LC3A, MAP1LC3B and GABARAP.
    亚细胞定位Mitochondrion outer membrane; Multi-pass membrane protein.
    组织特异性Widely expressed.
    翻译后修饰Phosphorylation at Tyr-18 by SRC inhibits activation of mitophagy. Following hypoxia, dephosphorylated at Tyr-18, leading to interaction with MAP1 LC3 family proteins and triggering mitophagy.
    相似性Belongs to the FUN14 family.
    功能Acts as an activator of hypoxia-induced mitophagy, an important mechanism for mitochondrial quality control.
    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FUNDC1 is a 155 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC1 maps to human chromosome Xp11.3 and mouse chromosome X A1.2. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

     

    应用推荐稀释比例
    {WB}{1:300-800}

     

    产品细节图片1
    Sample:
    Lane 1: Mouse Cerebellum tissue lysates
    Lane 2: Mouse Heart tissue lysates
    Lane 3: Human 293T cell lysates
    Lane 4: Human MCF-7 cell lysates
    Lane 5: Human A549 cell lysates
    Primary: Anti-FUNDC1 (bs-13227R) at 1/800 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 17 kDa
    Observed band size: 17 kDa

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    图标文献和实验
    该产品被引用文献

    [IF={{ 9.8 }}] {Jian Li. et al. FUNDC1-mediated mitophagy triggered by mitochondrial ROS is partially involved in 1-nitropyrene-evoked placental progesterone synthesis inhibition and intrauterine growth retardation in mice. SCI TOTAL ENVIRON. 2024 Jan;908:168383} {WB} {Human}

    [IF={{ 8.2 }}] {Sen Zeng. et al. Role of OGDH in Atophagy-IRF3-IFN-β pathway during classical swine fever virus infection. INT J BIOL MACROMOL. 2023 Sep;249:126443} {WB} {Pig}

    [IF={{ 7.2 }}] {Lan Gao. et al. c-FLIP Protects Cardiac Microcirculation in Sepsis-Induced Myocardial Dysfunction Via FUNDC1-Mediated Regulation of Mitochondrial Autophagy. JACC-BASIC TRANSL SC. 2025 May;:} {IF} {Rat}

    [IF={{ 4.011 }}] {Xu G et al. Fundc1 is necessary for proper body axis formation during embryogenesis in zebrafish. Sci Rep. 2019 Dec 11;9(1):18910.} {WB} {grass carp&Human}

    [IF={{ 3.3 }}] {Tang Lihua. et al. FUNDC1 predicts Poor Prognosis and promotes Progression and Chemoresistance in Endometrial Carcinoma. J CANCER. 2024 Oct;15(20):6490-6504} {IHC} {Human}

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    文献支持
    FUNDC1 Rabbit pAb(bs-13227R)-50ul/100ul
    ¥1180 - 1980