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CUL4B Antibody

  • 货号：
    CSB-PA005106
  • 规格：
    ￥880
  • 图片：
    • Western Blot analysis of mouse liver mouse kidney mouse heart cells using CUL-4B Polyclonal Antibody
  • 其他：

产品详情

  • Uniprot No.：
    Q13620
  • 基因名：
  • 别名：
    CUL 4B antibody; CUL-4B antibody; CUL4B antibody; CUL4B_HUMAN antibody; Cullin-4B antibody; DKFZp686F1470 antibody; KIAA0695 antibody; MRXHF2 antibody; MRXSC antibody; SFM2 antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human,Mouse,Rat
  • 免疫原：
    Synthesized peptide derived from the Internal region of Human CUL-4B.
  • 免疫原种属：
    Homo sapiens (Human)
  • 标记方式：
    Non-conjugated
  • 抗体亚型：
    IgG
  • 纯化方式：
    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 产品提供形式：
    Liquid
  • 应用范围：
    WB, ELISA
  • 推荐稀释比：
    Application Recommended Dilution
    WB 1:500-1:2000
    ELISA 1:20000
  • 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：
    Core component of multiple cullin-RING-based E3 ubiquitin-protein ligase complexes which mediate the ubiquitination and subsequent proteasomal degradation of target proteins. The functional specificity of the E3 ubiquitin-protein ligase complex depends on the variable substrate recognition subunit. CUL4B may act within the complex as a scaffold protein, contributing to catalysis through positioning of the substrate and the ubiquitin-conjugating enzyme. Plays a role as part of the E3 ubiquitin-protein ligase complex in polyubiquitination of CDT1, histone H2A, histone H3 and histone H4 in response to radiation-induced DNA damage. Targeted to UV damaged chromatin by DDB2 and may be important for DNA repair and DNA replication. A number of DCX complexes (containing either TRPC4AP or DCAF12 as substrate-recognition component) are part of the DesCEND (destruction via C-end degrons) pathway, which recognizes a C-degron located at the extreme C terminus of target proteins, leading to their ubiquitination and degradation. The DCX(AMBRA1) complex is a master regulator of the transition from G1 to S cell phase by mediating ubiquitination of phosphorylated cyclin-D (CCND1, CCND2 and CCND3). The DCX(AMBRA1) complex also acts as a regulator of Cul5-RING (CRL5) E3 ubiquitin-protein ligase complexes by mediating ubiquitination and degradation of Elongin-C (ELOC) component of CRL5 complexes. Required for ubiquitination of cyclin E (CCNE1 or CCNE2), and consequently, normal G1 cell cycle progression. Regulates the mammalian target-of-rapamycin (mTOR) pathway involved in control of cell growth, size and metabolism. Specific CUL4B regulation of the mTORC1-mediated pathway is dependent upon 26S proteasome function and requires interaction between CUL4B and MLST8. With CUL4A, contributes to ribosome biogenesis.
  • 基因功能参考文献：
    1. Results show that CUL4B is highly expressed in pancreatic cancer cells and inversely correlated with miR-300 expression which activate the Wnt/beta-catenin signaling pathway and further stimulating EMT, thus promoting proliferation and migration but suppressing apoptosis of pancreatic cancer cells. PMID: 28685847
    2. The CUL4B interacts with WD-40 proteins through the adaptor protein DNA damage-binding protein 1 (DDB1) to target substrates for ubiquitylation. PMID: 28886238
    3. This study found that microRNA-194 (miR-194) and CUL4B protein were inversely correlated in cancer specimens and demonstrated that miR-194 could downregulate CUL4B by directly targeting its 3'-UTR. PMID: 28164432
    4. findings revealed that CUL4A and CUL4B are differentially associated with etiologic factors for pulmonary malignancies and are independent prognostic markers for the survival of distinct lung cancer subtypes PMID: 27974468
    5. CUL4B regulates protein turnover and homeostasis in response to dopamine stimulation. PMID: 28225217
    6. CUL4B protein levels in human subcutaneous adipose tissue is negatively correlated with body mass index. PMID: 27899484
    7. these results suggest that knockdown of CUL4B inhibited the proliferation and invasion through suppressing the Wnt/beta-catenin signaling pathway in NSCLC cells. Therefore, CUL4B may represent a novel therapeutic target for the treatment of NSCLC. PMID: 27656838
    8. these results showed that knockdown of CUL4B inhibit proliferation and promotes apoptosis of colorectal cancer cells through suppressing the Wnt/beta-catenin signaling pathway PMID: 26617747
    9. Our data are consistent with the idea that the CUL4A/B-DDB1-CRBN complex catalyses the polyubiquitination and thus controls the degradation of CLC-1 channels. PMID: 26021757
    10. FBXO44-mediated degradation of RGS2 protein uniquely depends on a Cul4B/DDB1 complex. PMID: 25970626
    11. results established a critical role of CUL4B in negatively regulating the p53-ROS positive feedback loop that drives cellular senescence PMID: 25464270
    12. Results demonstrated that CUL4B promotes cell proliferation and inhibits the apoptosis of osteosarcoma cells. PMID: 25189186
    13. Results show that CUL4A- and CUL4B-mediated polyubiquitination of gamma-tubulin for its degradation. PMID: 25542213
    14. Data show that CUL4B variants are associated with a wide range of cerebral malformations and suggest an important role in brain through its interaction with WDR62, a protein in which variants were identified in patients with cerebral malformations. PMID: 25385192
    15. Cullin4B-Ring E3 ligase complex (CRL4B) is physically associated with PRC2. CRL4B possesses an intrinsic transcription repressive activity by promoting H2AK119 monoubiquitination. CUL4B promotes cancer cell proliferation, invasion, and tumorigenesis in vitro and in vivo. PMID: 23238014
    16. CUL4B can up-regulate Wnt/beta-catenin signalling in human HCC through transcriptionally repressing Wnt antagonists and thus contributes to the malignancy of HCC. PMID: 25430888
    17. The intellectual disability phenotype is caused by aberrant splicing and removal of intron 7 from CUL4B gene primary transcript. PMID: 24898194
    18. CRL4B promotes tumorigenesis by coordinating with SUV39H1/HP1/DNMT3A in DNA methylation-based epigenetic silencing PMID: 24292684
    19. these observations establish an important negative regulatory role of CUL4B on p53 stability. PMID: 24452595
    20. HIV-1 Vpr can trigger G2 cell cycle arrest in the absence of either CUL4A or CUL4B. PMID: 24719410
    21. Investigated CUL4B expression pattern in patients with colon cancer; immunohistochemistry and PCR study showed that high CUL4B expression was significantly associated with colon cancer progression and pathogenesis. PMID: 23649548
    22. Studies indicate Jun activation domain-binding protein Jab1 as a substrate for CUL4B E3 ligase. PMID: 23357576
    23. Our results suggest that XLID CUL4B mutants are defective in promoting TSC2 degradation and positively regulating mTOR signaling in neocortical neurons PMID: 23348097
    24. the up-regulation of CDK2 by CUL4B is achieved via the repression of miR-372 and miR-373, which target CDK2. PMID: 23479742
    25. The data suggest that unneddylated Cul4B isoforms specifically inhibits beta-catenin degradation during mitosis. PMID: 22992378
    26. the unexpected association of defective CUL4B with syndromal X-linked mental retardation in humans PMID: 21352845
    27. Cullin 4B protein ubiquitin ligase targets peroxiredoxin III for degradation. PMID: 21795677
    28. CUL4B targets WDR5 for ubiquitylation and degradation in the nucleus. PMID: 21816345
    29. Increased PRMT5 activity mediates key events associated with cyclin D1-dependent neoplastic growth, including CUL4 repression, CDT1 overexpression, and DNA rereplication. PMID: 20951943
    30. This study identifies CRL4-Cdt2 ubiquitin ligase to promote the ubiquitin-dependent proteolysis of the histone H4 methyltransferase Set8 during S-phase of the cell cycle and after UV-irradiation in a reaction that is dependent on PCNA. PMID: 20932471
    31. the interplay between CUL4A and CUL4B in pathogenesis of CUL4B-deficiency in humans PMID: 20064923
    32. CUL4B is over-expressed in placenta in intra-uterine growth restriction. PMID: 20005570
    33. The CUL4B gene is associated with X-linked mental retardation syndrome. PMID: 20002452
    34. Data show that that RNA interference of CUL4B led to an inhibition of cell proliferation and a prolonged S phase, due to the overaccumulation of cyclin E. PMID: 19801544
    35. Studies indicate that CUL4 uses a large beta-propeller protein, DDB1, as a linker to interact with a subset of WD40 proteins. PMID: 19818632
    36. human CUL4B and cyclin E proteins interact with each other and the CUL4B complexes can polyubiquitinate the CUL4B-associated cyclin E PMID: 16322693
    37. Cul4B, PCNA, and DDB1 are involved in the degradation of Cdt1 after ultraviolet radiation PMID: 16407252
    38. The relatively high frequency of CUL4B mutations in this series indicates that it is one of the most commonly mutated genes underlying XLMR and suggests that its introduction into clinical diagnostics should be a high priority. PMID: 17236139
    39. Mutation in CUL4B causes X-linked mental retardation PMID: 17273978
    40. a fat-soluble ligand-dependent ubiquitin ligase complex in human cell lines, in which dioxin receptor (AhR) is integrated as a component of a novel cullin 4B ubiquitin ligase complex, CUL4B(AhR) PMID: 17392787
    41. CUL4-DDB1 ubiquitin ligase interacts with Raptor and regulates the mTORC1-mediated signaling pathway through ubiquitin-dependent proteolysis. PMID: 18235224
    42. DDB1-CUL4B(DDB2) E3 ligase may have a distinctive function in modifying the chromatin structure at the site of UV lesions to promote efficient NER. PMID: 18593899
    43. CUL4A and CUL4B are therefore components of a conserved Wnt-induced proteasome targeting (WIPT) complex that regulates p27(KIP1) levels and cell cycle progression in mammalian cells. PMID: 19056892
    44. Cells depleted of Dda1 spontaneously accumulated double-stranded DNA breaks in a similar way to Cul4A-, Cul4B- or Wdr23-depleted cells, indicating that Dda1 interacts physically and functionally with cullin-RING E3 ligases complexes. PMID: 19295130

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  • 相关疾病：
    Mental retardation, X-linked, syndromic, 15 (MRXS15)
  • 亚细胞定位：
    Nucleus.
  • 蛋白家族：
    Cullin family
  • 数据库链接：

    HGNC: 2555

    OMIM: 300304

    KEGG: hsa:8450

    STRING: 9606.ENSP00000384109

    UniGene: Hs.102914