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  4. SMC3 Recombinant Monoclonal Antibody

SMC3 Recombinant Monoclonal Antibody

  • 中文名稱：
    SMC3 Recombinant Monoclonal Antibody
  • 貨號：
    CSB-RA212321A0HU
  • 規格：
    ￥1320
  • 圖片：
    • Flow cytometric analysis of SMC3 expression in HepG2 cells using SMC3 antibody. Green, isotype control; red, SMC3.
    • Immunocytochemical staining of HepG2 cells with SMC3 antibody. Nuclei were stained blue with DAPI; SMC3 was stained magenta with Alexa Fluor? 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Scale bar, 20 μm.
    • Immunohistochemistry was performed on paraffin-embedded human sigmoid colon carcinoma using SMC3 antibody. Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
    • Western blotting analysis using SMC3 antibody. Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with SMC3 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively.
  • 其他：

產品詳情

  • Uniprot No.：
  • 基因名：
  • 別名：
    SMC3; Structural Maintenance Of Chromosomes 3; SMC3L1; HCA; BAM; Bamacan; CSPG6; Basement Membrane-Associated Chondroitin Proteoglycan; Structural Maintenance Of Chromosomes Protein 3; Chondroitin Sulfate Proteoglycan 6 (Bamacan); Chromosome-Associated Polypeptide; SMC Protein 3; BMH; Chondroitin Sulfate Proteoglycan 6; Bamacan Proteoglycan; CDLS3; SMC-3
  • 反應種屬：
    Human, Mouse, Rat
  • 免疫原：
    Recombinant Human SMC3 protein
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標記方式：
    Non-conjugated
  • 克隆類型：
    Monoclonal
  • 抗體亞型：
    Rabbit IgG
  • 純化方式：
    Affinity-chromatography
  • 克隆號：
    12G8
  • 濃度：
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液：
    Rabbit IgG in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.
  • 產品提供形式：
    Liquid
  • 應用范圍：
    ELISA, WB, FC, ICC, IHC
  • 推薦稀釋比：
    Application Recommended Dilution
    WB 1:1000-1:5000
    FC 1:200-1:2000
    ICC 1:100-1:1000
    IHC 1:100-1:200
  • Protocols：
  • 儲存條件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期：
    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.
  • 用途：
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

  • 功能：
    Central component of cohesin, a complex required for chromosome cohesion during the cell cycle. The cohesin complex may form a large proteinaceous ring within which sister chromatids can be trapped. At anaphase, the complex is cleaved and dissociates from chromatin, allowing sister chromatids to segregate. Cohesion is coupled to DNA replication and is involved in DNA repair. The cohesin complex plays also an important role in spindle pole assembly during mitosis and in chromosomes movement.
  • 基因功能參考文獻：
    1. H2 inhibited lung cancer progression through down-regulating SMC3. PMID: 29852353
    2. We identified a large number of mutations in the CC region of both Smc1 and Smc3... we introduced them to the yeast Smc1 and Smc3 CC domains and characterized the effect of these mutant alleles on cohesin's function. We identified a missense mutation in the region of the kink domain of Smc3, which was previously identified in kidney carcinoma PMID: 27307603
    3. Results show that SMC3 is upregulated in asthma patients and suggest that it may play an important role in atopic asthma development, especially in asthma epithelial-mesenchymal transition. PMID: 25515564
    4. Data show that histone deacetylase 8 (HDAC8) inhibition led to accumulation of acetylated-SMC3 protein but had no influence on the transcription of estrogen-responsive genes. PMID: 27072133
    5. De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypes PMID: 25655089
    6. cohesin's proposed DNA exit gate is formed by interactions between Scc1 and the coiled-coil region of Smc3. PMID: 25414306
    7. Cross-sectional deep-sequencing analysis for clonal hierarchy demonstrated STAG2, SMC3, and RAD21 mutations to be ancestral in 18%, 18%, and 47% of cases, respectively, and each expanded to clonal dominance concordant with disease transformation PMID: 25006131
    8. Mutations in SMC3 is associated with acute myeloid leukemia. PMID: 24335498
    9. Upon knock-down of human SMC1, much of SMC3 remains stable, accumulates in the cytoplasm and does not associate with other cohesin proteins. PMID: 23776448
    10. SMC3 and separase are upregulated and securin is downregulated in malignant transformation of BEAS-2B cells induced by coal tar pitch smoke extracts. PMID: 21126432
    11. these studies clearly suggest that bamacan interacts with the vaccinia virus-N1L and such interactions seem to play a positive role in promoting the viral growth and perhaps contribute to the virulence of VV in neural cells. PMID: 19444697
    12. identification as target for beta-catenin/T-cell factor 4 transactivation pathway PMID: 12651860
    13. Hinderin is a novel binding partner of SMC3. Based on its ability to modulate SMC1/SMC3 interaction we postulate that Hinderin affects the availability of SMC3 to engage in the formation of multimeric protein complexes PMID: 15656913
    14. RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC3. PMID: 16043481
    15. RhoB and cAMP cis-acting response elements -BPa two known oncogenic mediators whose expression is significantly increased following SMC3 overexpression play a significant role in mediating SMC3 tumorigenesis PMID: 16156898
    16. SMC3 deficiency affects chromosomal stability leading to the activation of p53-dependent mitotic checkpoint. PMID: 17081288
    17. Mutations in SMC3 cause a mild variant of cornelia de Lange syndrome with predominant mental retardation PMID: 17273969
    18. phosphorylation of a core cohesin subunit SMC3 by ATM plays an important role in DNA damage PMID: 18442975
    19. This study identified a molecular target for the acetyltransferase Eco1 and revealed that Smc3 acetylation is a conserved mechanism in regulating sister chromatid cohesion. PMID: 18614053
    20. There were greater levels of chondroitin sulphate WF6 epitope in gingival crevicular fluid from destructive sites of patients with chronic periodontitis compared with non-destructive sites of patients with gingivitis or chronic periodontitis. PMID: 18727658
    21. Data describe alterations of myocardial intercellular and cell-matrix contacts in hypertrophic tissue, and show intracellular translocation of beta-catenin, alpha-actinin and chondroitin sulfate proteoglycan 6 in both an animal model and in LVH patients. PMID: 19094982

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  • 相關疾病：
    Cornelia de Lange syndrome 3 (CDLS3)
  • 亞細胞定位：
    Nucleus. Chromosome. Chromosome, centromere.
  • 蛋白家族：
    SMC family, SMC3 subfamily
  • 數據庫鏈接：

    HGNC: 2468

    OMIM: 606062

    KEGG: hsa:9126

    STRING: 9606.ENSP00000354720

    UniGene: Hs.24485