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        1. 靶點科技(北京)有限公司

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          Kerafast ENH001 Anti-DNA-RNA Hybrid [S9.6] Antibody

          時間:2022/10/1閱讀:176
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          Kerafast  ENH001 Anti-DNA-RNA Hybrid [S9.6] Antibody 針對ΦX174噬菌體衍生的合成DNA-RNA抗原產生該小鼠單克隆抗體,并識別各種長度的RNA-DNA雜交體。

           

          產品特色:

          • 對DNA-RNA雜交體具有高度特異性和親和力

          • 可用于檢測R環(huán)

          • 不與單鏈DNA或雙鏈DNA交叉反應

          • 對于富含AU的雙鏈RNA,已觀察到輕微的交叉反應(約5倍)。

          • 對于長度為8,10,15和23個堿基對的雜交體顯示出高親和力結合

          DNA-RNA雜合體是真核細胞中的天然存在,這些za種的水平在具有高轉錄活性的位點增加,例如在轉錄起始,抑制和延伸期間。由于RNA-DNA雜交體影響基因組不穩(wěn)定性,S9.6抗體是一種有用的試劑,可幫助研究這些za種在DNA復制或其他細胞過程中形成的R環(huán)和損傷的后果。此外,S9.6抗體可有效識別用于微陣列研究的RNA-DNA雜交。

          背景介紹:

          DNA-RNA hybrids are a natural occurrence within eukaryotic cells, with levels of these hybrids increasing at sites with high transcriptional activity, such as during transcription initiation, repression, and elongation. Because RNA-DNA hybrids influence genomic instability, the S9.6 antibody is a useful reagent to help study the consequences of R-loops and lesions formed by these hybrids during DNA replication or other cellular processes. In addition, the S9.6 antibody is effective in recognizing RNA-DNA hybridization for microarray studies。

          產品詳情:

          Product Type:Antibody
          Name:Anti-DNA-RNA Hybrid [S9.6]
          Antigen:S9.6 ΦX174 bacteriophage-derived synthetic DNA–RNA antigen
          Isotype:Rabbit IgG
          Fusion Tag(s):Mouse Fab version contains His-tag
          Clone Name:S9.6
          Reactivity:High specificity and affinity for DNA/RNA hybrids and other A-form nucleic acid hybrids
          Immunogen:ΦX174 bacteriophage-derived synthetic DNA/RNA
          Purification Method:Protein A/G
          Buffer:ENHOO1: PBS, 0.05% (w/v) Sodium Azide
          Ab01137- : PBS with 0.02% Proclin 300
          Tested Applications:

          Dot Blot Analysis: 0.2 µg/mL.
          Affinity Binding Assay: Clone S9.6 bound the DNA-RNA heteropolymer and poly(I)-poly(dC) equally, but 100-fold higher levels of poly(A)-poly(dT) were required to achieve a similar degree of binding. Single-stranded DNA, double-stranded DNA and RNA, and ribosomal RNA were not bound by clone S9.6 (Boguslawski, S.J., et al. (1986). J. Immunol Methods. 89(1):123-130).
          Chromatin Immunoprecipitation (ChIP) Analysis: A representative lot detected increased DNA RNA hybrids at four actively transcribed genes upon shRNA-mediated knockdown of BRCA1 or BRCA2, but not PCID2 or RAD51 in HeLa cells (Bhatia, V., et al. (2014). Nature. 511(7509):362-365).
          Chromatin Immunoprecipitation (ChIP) Analysis: A representative lot detected R-loops formed over beta-actin gene using HeLa chromatin preparation. RNase H treatment of the chromatin preparation prevented clone S9.6 from immunoprecipitating target chromatin fragments (Skourti-Stathaki, K., et al. (2011). Mol. Cell. 42(6):794-805).
          Chromatin Immunoprecipitation-sequencing (ChIP-seq) Analysis: A representative lot detected genome-wide distribution of DNA-RNA hybrids in budding yeast by ChIP-seq analysis (El Hage, A., et al. (2014). PLoS Genet. 10(10):e1004716).
          Immunocytochemistry Analysis: Representative lots immunolocalized nuclear R loops by fluorescent immunocytochemistry staining of methanol-fixed H1 human embryonic stem cells (hESCs) and formaldehyde-fixed HeLa cells (Bhatia, V., et al. (2014). Nature. 511(7509):362-365; Ginno, P.A., et al. (2012). Mol. Cell. 45(6):814-825).
          Immunoprecipitation Analysis: A representative lot immunoprecipitated in vitro transcribed R-loop substrate (DNA-RNA hybrid), but not doouble-stranded DNA (dsDNA) (Ginno, P.A., et al. (2012). Mol. Cell. 45(6):814-825).


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