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FANCI Antibody

  • 货号：
    CSB-PA008420GA01HU
  • 规格：
    ￥3,900
  • 其他：

产品详情

  • Uniprot No.：
    Q9NVI1
  • 基因名：
    FANCI
  • 别名：
    FANCI antibody; FANCI gene antibody; FANCI_HUMAN antibody; Fanconi anemia group I protein antibody; Fanconi anemia; complementation group I antibody; FLJ10719 antibody; FLJ14658 antibody; KIAA1794 antibody; Protein FACI antibody; Protein FANCI antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human
  • 免疫原：
    Human FANCI
  • 免疫原种属：
    Homo sapiens (Human)
  • 抗体亚型：
    IgG
  • 纯化方式：
    Antigen Affinity purified
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
  • 产品提供形式：
    Liquid
  • 应用范围：
    ELISA,WB,IF
  • Protocols：
  • 储存条件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 货期：
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

产品评价

靶点详情

  • 功能：
    Plays an essential role in the repair of DNA double-strand breaks by homologous recombination and in the repair of interstrand DNA cross-links (ICLs) by promoting FANCD2 monoubiquitination by FANCL and participating in recruitment to DNA repair sites. Required for maintenance of chromosomal stability. Specifically binds branched DNA: binds both single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA). Participates in S phase and G2 phase checkpoint activation upon DNA damage.
  • 基因功能参考文献：
    1. BRMS1FANCI interaction is necessary for the regulatory role of BRMS1 in the FA pathway. PMID: 30365131
    2. Study reports the first structural insight into the human FANCD2-FANCI complex by obtaining the cryo-EM structure. The complex contains an inner cavity, large enough to accommodate a double-stranded DNA helix, as well as a protruding Tower domain. Disease-causing mutations in the Tower domain are observed in several Fanconi anemia patients. PMID: 27405460
    3. FANCI phosphorylation activates the FANCI/D2 complex. PMID: 28636932
    4. Data suggest that FANCI and FANCD2 have partially non-overlapping and possibly even opposing roles during the replication stress response. PMID: 29059323
    5. Fanconi anemia FANCD2 and FANCI proteins regulate the nuclear dynamics of splicing factors, such as SF3B1. PMID: 29030393
    6. FANCB dimer coordinates FANCD2:FANCI monoubiquitination by two FANCL RING-ligases. Deubiquitination of FANCD2:FANCI by USP1:UAF1 occurs only when DNA is removed. PMID: 27986371
    7. depletion of FANCI, but not FANCD2 or USP1, results in increased phosphorylation and activation of Akt. PMID: 27097374
    8. FANCI mutations are associated with Fanconi anemia in VACTERL association. PMID: 26590883
    9. FANCJ protein is important for the stability of FANCD2/FANCI proteins and protects them from proteasome and caspase-3 dependent degradation. PMID: 26336824
    10. These findings indicate that FANCI functions upstream of FA core complex recruitment independently of FANCD2, and alter the current view of the FA-BRCA pathway. PMID: 26430909
    11. these purification methods for human FANCI and FANCD2 provide novel procedures to facilitate structural and biochemical studies of human FANCI and FANCD2. PMID: 25168188
    12. Results show that ATR-mediated phosphorylation of FANCI, controls dormant origin firing in response to DNA replication stress. PMID: 25843623
    13. Our studies reveal a previously unknown mechanism for the coordinate nuclear import of a subset of FANCD2 and FANCI, a key early step in the cellular ICL response. PMID: 24278431
    14. Mutations in FANCI that impair its DNA binding activity compromise DNA-stimulated FANCD2 monoubiquitination. PMID: 24623813
    15. A CUE ubiquitin-binding domain in the FANCD2 protein is required for interaction with FANCI, retention of monoubiquitinated FANCD2, and FANCI in chromatin, and for efficient DNA interstrand crosslinks repair. PMID: 22855611
    16. These data suggest a key role for the E3 ligase activity of RAD18 in the recruitment of FANCD2 and FANCI to chromatin and the events leading to their ubiquitylation during S phase. PMID: 21355096
    17. although proper nuclear localization of FANCI is crucial for robust FANCD2 monoubiquitination, the putative FANCI EDGE motif is important for DNA crosslink repair PMID: 20971953
    18. study characterizes FANI which promotes DNA interstrand cross-linking repair in a manner strictly dependent on its ability to accumulate at or near sites of DNA damage and that relies on mono-ubiquitylation of the FANCI-FANCD2 complex PMID: 20671156
    19. description of the Fanconi anemia protein FANCI, identified as an ATM/ATR kinase substrate required for resistance to mitomycin C; it associates with FANCD2 and, together, as the FANCI-FANCD2 (ID) complex, localizes to chromatin in response to DNA damage PMID: 17412408
    20. These data add up to two conclusions. First, KIAA1794 is a Fanconi anemia gene. Second, this gene is identical to FANCI, since the patient cell lines found mutated in this study included the reference cell line for group I, EUFA592. PMID: 17452773
    21. FANCI, a member of the Fanconi anemia pathway, is monoubiquitinated in a site-specific and DNA damage dependent manner. PMID: 17460694
    22. Results suggest that the multiple phosphorylation of FANCI serves as a molecular switch in activation of the Fanconi anemia pathway. PMID: 18931676
    23. This work therefore establishes a system that provides mechanistic insight into the functions of FANCL and FANCI in the catalysis of FANCD2 monoubiquitination. PMID: 19111657
    24. Data show that FANCD2 and FANCI specifically associate with common fragile site loci irrespective of whether the chromosome is broken, and that these loci are frequently interlinked through BLM-associated ultra-fine DNA bridges through mitosis. PMID: 19465922
    25. the FANCI-FANCD2 complex may participate in repair of damaged replication forks through its preferential recognition of branched structures. PMID: 19561358
    26. results rule out a major role of FANCI in familial breast cancer susceptibility PMID: 19737859

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  • 相关疾病：
    Fanconi anemia complementation group I (FANCI)
  • 亚细胞定位：
    Nucleus. Cytoplasm. Note=Observed in spots localized in pairs on the sister chromatids of mitotic chromosome arms and not centromeres, one on each chromatids. These foci coincide with common fragile sites. They are frequently interlinked through BLM-associated ultra-fine DNA bridges.
  • 数据库链接：

    HGNC: 25568

    OMIM: 609053

    KEGG: hsa:55215

    STRING: 9606.ENSP00000310842

    UniGene: Hs.513126