Here's how LINK.SPRINGER.COM makes money* and how much!

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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Schema
  9. External Links
  10. Analytics And Tracking
  11. Libraries

We are analyzing https://link.springer.com/protocol/10.1385/1-59259-828-5:099.

Title:
Site-Specific Analysis of Histone Methylation and Acetylation | SpringerLink
Description:
Covalent modifications on the nucleosomal histones are essential in chromatin regulation and gene expression. Patterns of histone modifications may be somatically maintained and can thereby maintain locus-specific repression/activity in defined lineages or throughout...
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Telecommunications

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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How Does Link.springer.com Make Money? {💸}

We see no obvious way the site makes money.

Earning money isn't the goal of every website; some are designed to offer support or promote social causes. People have different reasons for creating websites. This might be one such reason. Link.springer.com could be getting rich in stealth mode, or the way it's monetizing isn't detectable.

Keywords {🔍}

histone, google, scholar, article, pubmed, cas, methylation, acetylation, chromatin, cell, analysis, protocol, chapter, cells, genet, embo, lysine, privacy, cookies, content, information, publish, goto, feil, genes, heterochromatin, allis, search, protocols, molecular, patterns, genome, regions, mouse, science, biol, nat, press, download, usd, personal, data, log, journal, research, epigenetics, umlauf, book, biology, modifications,

Topics {✒️}

hypoxia-induced epithelial–mesenchymal transition maintain locus-specific repression/activity eed-enx1 polycomb-group complexes chicken β-globin locus month download article/chapter allele-specific nuclease sensitivity single-strand conformation polymorphisms formaldehyde-crosslinked-chromatin-immunoprecipitation pcr-sscp based assay site-specific analysis epigenetics protocols cold spring harbor privacy choices/manage cookies device instant download histone lysine methylation mouse hematopoietic stem polycomb-group silencing pcr-based assays imprinted mouse genes heterochromatin domain boundaries quantitative chromatin immunoprecipitation histone modification analysis dimensional gel analysis mapping chromosomal proteins hot-stop pcr histone h3 methylation coding regions humana press hp1 chromo domain core histone hyperacetylation journal finder publish native chromatin prepared immunoprecipitated chromatin fractions imprinted genes snrpn european economic area differentiation-independent manner methylated n-terminus pericentric heterochromatin involves differentially methylated forms core histone acetylation transcriptionally active chromatin conditions privacy policy nucleic acids res analyze histone methylation independent dynamic regulation acetylation distinguish active accepting optional cookies higher-order structure early gene induction protocol umlauf

Schema {🗺️}

ScholarlyArticle:
      headline:Site-Specific Analysis of Histone Methylation and Acetylation
      pageEnd:120
      pageStart:99
      image:https://media.springernature.com/w153/springer-static/cover/book/978-1-59259-828-1.jpg
      genre:
         Springer Protocols
      isPartOf:
         name:Epigenetics Protocols
         isbn:
            978-1-59259-828-1
            978-1-58829-336-7
         type:Book
      publisher:
         name:Humana Press
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:David Umlauf
            affiliation:
                  name:CNRS UMR-5535 and University of Montpellier II
                  address:
                     name:Institute for Molecular Genetics, CNRS UMR-5535 and University of Montpellier II, Montpellier, France
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Yuji Goto
            affiliation:
                  name:CNRS UMR-5535 and University of Montpellier II
                  address:
                     name:Institute for Molecular Genetics, CNRS UMR-5535 and University of Montpellier II, Montpellier, France
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Robert Feil
            affiliation:
                  name:CNRS UMR-5535 and University of Montpellier II
                  address:
                     name:Institute for Molecular Genetics, CNRS UMR-5535 and University of Montpellier II, Montpellier, France
                     type:PostalAddress
                  type:Organization
            type:Person
      keywords:Chromatin immunoprecipitation, native chromatin, histone methylation, histone acetylation, quantitative PCR, allele-specific PCR
      description:Covalent modifications on the nucleosomal histones are essential in chromatin regulation and gene expression. Patterns of histone modifications may be somatically maintained and can thereby maintain locus-specific repression/activity in defined lineages or throughout development. During recent years, histone acetylation and methylation have emerged as key players in the repression or activation of genes and chromosomal domains. Histone methylation and acetylation patterns (and other histone modifications) can be analyzed by chromatin immunoprecipitation (ChIP). This chapter describes how ChIP can be performed on native chromatin prepared from cells and tissues, in order to analyze histone methylation and acetylation at specific sites in the genome. We also present different PCR-based assays that can be applied to analyze loci of interest in immunoprecipitated chromatin fractions.
      datePublished:2004
      isAccessibleForFree:
      hasPart:
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         cssSelector:.main-content
         type:WebPageElement
      context:https://schema.org
Book:
      name:Epigenetics Protocols
      isbn:
         978-1-59259-828-1
         978-1-58829-336-7
Organization:
      name:Humana Press
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:CNRS UMR-5535 and University of Montpellier II
      address:
         name:Institute for Molecular Genetics, CNRS UMR-5535 and University of Montpellier II, Montpellier, France
         type:PostalAddress
      name:CNRS UMR-5535 and University of Montpellier II
      address:
         name:Institute for Molecular Genetics, CNRS UMR-5535 and University of Montpellier II, Montpellier, France
         type:PostalAddress
      name:CNRS UMR-5535 and University of Montpellier II
      address:
         name:Institute for Molecular Genetics, CNRS UMR-5535 and University of Montpellier II, Montpellier, France
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:David Umlauf
      affiliation:
            name:CNRS UMR-5535 and University of Montpellier II
            address:
               name:Institute for Molecular Genetics, CNRS UMR-5535 and University of Montpellier II, Montpellier, France
               type:PostalAddress
            type:Organization
      name:Yuji Goto
      affiliation:
            name:CNRS UMR-5535 and University of Montpellier II
            address:
               name:Institute for Molecular Genetics, CNRS UMR-5535 and University of Montpellier II, Montpellier, France
               type:PostalAddress
            type:Organization
      name:Robert Feil
      affiliation:
            name:CNRS UMR-5535 and University of Montpellier II
            address:
               name:Institute for Molecular Genetics, CNRS UMR-5535 and University of Montpellier II, Montpellier, France
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Institute for Molecular Genetics, CNRS UMR-5535 and University of Montpellier II, Montpellier, France
      name:Institute for Molecular Genetics, CNRS UMR-5535 and University of Montpellier II, Montpellier, France
      name:Institute for Molecular Genetics, CNRS UMR-5535 and University of Montpellier II, Montpellier, France
WebPageElement:
      isAccessibleForFree:
      cssSelector:.main-content

External Links {🔗}(127)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js

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