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CTCF Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年11月12日
  • W, IP, IF-IC, ChIP
  • Rabbit
  • H,M,R,Mk
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      CTCF Antibody

    • 抗原

      synthetic peptide corresponding to the carboxy terminus of the human CTCF protein

    • 应用范围

      W, IP, IF-IC, ChIP

    • 宿主

      Rabbit

    • 级别

      详见MSDS文件

    • 供应商

      CST

    • 保质期

      详见说明书

    • 适应物种

      H,M,R,Mk

    • 库存

      大量

    • 是否单克隆

      2

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting  IP=Immunoprecipitation  IF-IC=Immunofluorescence (Immunocytochemistry)  ChIP=Chromatin IP
    Reactivity Key:  H=Human  M=Mouse  R=Rat  Mk=Monkey
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Source
    W IP IF-IC ChIP H M R Mk Endogenous 140 Rabbit
    Protocols
    Specificity / Sensitivity

    CTCF Antibody detects endogenous levels of total CTCF protein. This antibody does not cross-react with BORIS.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the carboxy terminus of the human CTCF protein. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various cell lines using CTCF Antibody.

    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of HeLa cells using CTCF Antibody (green). Actin filaments have been labeled with DY-554 phalloidin (red).

    Chromatin IP

    Chromatin IP

    Chromatin immunoprecipitations were performed with cross-linked chromatin from 4 x 106 HeLa cells and either 20 μl of CTCF Antibody or 2 μl of Normal Rabbit IgG #2729 using SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003. The enriched DNA was quantified by real-time PCR using human c-Myc promoter primers, SimpleChIP® Human H19/Igf2 ICR Primers #5172, and SimpleChIP® Human α Satellite Repeat Primers #4486. The amount of immunoprecipitated DNA in each sample is represented as signal relative to the total amount of input chromatin, which is equivalent to one.


    Background

    CCCTC-binding factor (CTCF) and its paralog, the Brother of the Regulator of Imprinted Sites (BORIS), are highly conserved transcription factors that regulate transcriptional activation and repression, insulator function, and imprinting control regions (ICRs) (1-4). Although they have divergent amino and carboxy termini, both proteins contain 11 conserved zinc finger domains that work in combination to bind the same DNA elements (1). CTCF is ubiquitously expressed and contributes to transcriptional regulation of cell-growth regulated genes, including c-myc, p19/ARF, p16/INK4A, BRCA1, p53, p27, E2F1, and TERT (1). CTCF also binds to and is required for the enhancer-blocking activity of all known insulator elements and ICRs, including the H19/IgF2, Prader-Willi/Angelman syndrome, and Inactive X-Specific Transcript (XIST) anti-sense loci (5-7). CTCF DNA-binding is sensitive to DNA methylation, a mark that determines selection of the imprinted allele (maternal vs. paternal) (1). The various functions of CTCF are regulated by at least two different post-translational modifications. Poly(ADP-ribosyl)ation of CTCF is required for insulator function (8). Phosphorylation of Ser612 by protein kinase CK2 facilitates a switch of CTCF from a transcriptional repressor to an activator at the c-myc promoter (9). CTCF mutations or deletions have been found in many breast, prostate, and Wilms tumors (10,11). Expression of BORIS is restricted to spermatocytes and is mutually exclusive of CTCF (3). In cells expressing BORIS, promoters of X-linked cancer-testis antigens like MAGE-1A are demethylated and activated, but methylated and inactive in CTCF-expressing somatic cells (12). Like other testis specific proteins, BORIS is abnormally expressed in different cancers, such as breast cancer, and has a greater affinity than CTCF for DNA binding sites, detracting from CTCF’s potential tumor suppressing activity (1,3,13,14).

    1. Klenova, E.M. et al. (2002) Semin Cancer Biol 12, 399-414.
    2. Klenova, E.M. et al. (1993) Mol Cell Biol 13, 7612-24.
    3. Loukinov, D.I. et al. (2002) Proc Natl Acad Sci USA 99, 6806-11.
    4. Mukhopadhyay, R. et al. (2004) Genome Res 14, 1594-602.
    5. Hark, A.T. et al. (2000) Nature 405, 486-9.
    6. Ohta, T. et al. (1999) Am J Hum Genet 64, 397-413.
    7. Chao, W. et al. (2002) Science 295, 345-7.
    8. Yu, W. et al. (2004) Nat Genet 36, 1105-10.
    9. El-Kady, A. and Klenova, E. (2005) FEBS Lett 579, 1424-34.
    10. Filippova, G.N. et al. (1998) Genes Chromosomes Cancer 22, 26-36.
    11. Filippova, G.N. et al. (2002) Cancer Res 62, 48-52.
    12. Vatolin, S. et al. (2005) Cancer Res 65, 7751-62.
    13. Hong, J.A. et al. (2005) Cancer Res 65, 7763-74.
    14. D'Arcy, V. et al. (2008) Br J Cancer 98, 571-9.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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    图标文献和实验
    相关实验
    • Generation of Poly(ADP-ribosyl)ation Deficient Mutants of the Transcription Factor, CTCF

      of the PARylation mark. The latter was achieved by ectopic expression of mutated proteins in cells, followed by immunoprecipitation with the polyclonal anti-PAR antibody and Western analysis with a protein-specific antibody. The PARylation-deficient CTCF mutant

    • Generation of Antibody Molecules Through Antibody Engineering

      been overcome to a large extent using genetic-engineering techniques to produce chimeric mouse/human and completely human antibodies. Such an approach is particularly suitable because of the domain structure of the antibody molecule ( 2 ), where functional

    • The Antibody Molecule

      The importance of antibody molecules was first recognized in the 1890s, when it was shown that immunity to tetanus and diphtheria was caused by antibodies against the bacterial exotoxins (1 ). Around the same time, it was shown that antisera

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