{"id":9788,"date":"2026-10-15T08:33:30","date_gmt":"2026-10-15T08:33:30","guid":{"rendered":"https:\/\/www.mybiosource.com\/learn\/?page_id=9788"},"modified":"2026-10-15T08:33:30","modified_gmt":"2026-10-15T08:33:30","slug":"what-are-cell-cycle-regulators","status":"publish","type":"page","link":"https:\/\/www.mybiosource.com\/learn\/what-are-cell-cycle-regulators\/","title":{"rendered":"What Are Cell Cycle Regulators, and What Is Their Role in Cell Division?"},"content":{"rendered":"\n<style>.mbs-page, .mbs-page * { margin: 0; padding: 0; box-sizing: border-box; } html { scroll-behavior: smooth; } .mbs-page { font-family: -apple-system, BlinkMacSystemFont, 'Segoe UI', Roboto, sans-serif; line-height: 1.65; color: #1f2937; background: #fff; } .mbs-page img { max-width: 100%; } .mbs-page .wrap { max-width: 1140px; margin: 0 auto; padding: 0 1.25rem; } .mbs-page .nav { position: sticky; top: 0; z-index: 50; background: rgba(255,255,255,0.92); backdrop-filter: blur(8px); border-bottom: 1px solid #e5e7eb; 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gap: 2rem; } .mbs-page .site-footer h4 { color: #fff; font-size: 1rem; font-weight: 700; margin-bottom: 0.75rem; } .mbs-page .site-footer ul { list-style: none; padding: 0; margin: 0; } .mbs-page .site-footer li { margin-bottom: 0.5rem; } .mbs-page .site-footer a { color: #9ca3af; text-decoration: none; } .mbs-page .site-footer a:hover { color: #60a5fa; } .mbs-page .site-footer .bottom { max-width: 1200px; margin: 2.5rem auto 0; padding: 1.5rem 1.25rem 0; border-top: 1px solid rgba(255,255,255,0.12); font-size: 0.8125rem; color: #6b7280; } @media (min-width: 768px) {.mbs-page .site-footer .wrap { grid-template-columns: 2fr 1fr 1fr; } } .mbs-page .eyebrow { margin-bottom: 1rem; } .mbs-page .strip .n { font-size: 2rem; font-weight: 800; color: #bfdbfe; line-height: 1; margin-bottom: 0.5rem; } .mbs-page .flow-step .step { font-size: 0.75rem; letter-spacing: 0.12em; text-transform: uppercase; color: #2563eb; font-weight: 700; margin-bottom: 0.5rem; } .mbs-page .flow-step a, .mbs-page .tl-item a, .mbs-page .faq-item a, .mbs-page .cta p a, .mbs-page .section-head a { color: #1d4ed8; text-decoration: none; font-weight: 500; } .mbs-page .tile p + p { margin-top: 0.75rem; } .mbs-page .pick p + p { margin-top: 0.75rem; } .mbs-page .prose ul { margin: 0 0 1rem 1.25rem; max-width: 46rem; } .mbs-page .prose li { font-size: 1.0625rem; color: #374151; margin-bottom: 0.5rem; } .mbs-page .related p { display: contents; } .mbs-page .related a { flex-direction: row; } .mbs-page .related a .txt { flex: 1; display: block; } .mbs-page .related a .txt span { display: block; } .mbs-page .igtable td.hd { font-weight: 700; color: #0f172a; white-space: nowrap; } .mbs-page h1, .mbs-page h2, .mbs-page h3, .mbs-page h4 { padding: 0; } .mbs-page p { padding: 0; } .mbs-page a { text-decoration: none; } .mbs-page .cta h2 { color: #fff; line-height: 1.2; } .mbs-page .section-head h2, .mbs-page .tl-item h3, .mbs-page .flow-step h3, .mbs-page .pick h3, .mbs-page .tile h3, .mbs-page .faq-item h3 { line-height: 1.2; }<\/style>\n<p><script type=\"application\/ld+json\">{\"@context\": \"https:\/\/schema.org\", \"@type\": \"FAQPage\", \"mainEntity\": [{\"@type\": \"Question\", \"name\": \"What happens when cell cycle regulators malfunction?\", \"acceptedAnswer\": {\"@type\": \"Answer\", \"text\": \"When cell cycle regulators malfunction, cells either divide without proper checks or stall when they should keep dividing. The loss of a checkpoint lets cells with damaged DNA or misaligned chromosomes continue, which produces mutations and abnormal chromosome numbers (aneuploidy). Inherited mutations show the effect clearly: a faulty RB1 gene causes hereditary retinoblastoma, and a faulty TP53 gene causes Li-Fraumeni syndrome, which raises lifetime cancer risk. The opposite problem also occurs, because excess checkpoint signaling can push cells into senescence, a permanent arrest linked to tissue aging.\"}}, {\"@type\": \"Question\", \"name\": \"What is the restriction point, and why is it important?\", \"acceptedAnswer\": {\"@type\": \"Answer\", \"text\": \"The restriction point is the late G1 transition, after which a cell commits to dividing even if growth signals disappear. Arthur Pardee described it in 1974 after observing that mammalian cells deprived of growth factors stopped in G1, while cells past that point finished the cycle. The restriction point is important because it separates a reversible decision from an irreversible one: Rb phosphorylation flips a switch that makes E2F-driven gene expression self-sustaining. Cancer cells often bypass the need for growth signals, and their dependence on cyclin D-CDK4\/6 helps explain why CDK4\/6 inhibitors are effective.\"}}, {\"@type\": \"Question\", \"name\": \"What research tools are used to study cell cycle regulators?\", \"acceptedAnswer\": {\"@type\": \"Answer\", \"text\": \"Researchers measure how many cells are in each phase using flow cytometry, which measures DNA content with a fluorescent dye such as propidium iodide. EdU or BrdU incorporation labels cells in S phase, and phospho-histone H3 staining marks mitotic cells. Synchronization lets researchers study a single phase: a double thymidine block arrests cells at the G1\/S boundary, and nocodazole arrests them in mitosis. Western blotting tracks cyclin levels and Rb phosphorylation, and in vitro kinase assays measure CDK activity directly. Live-cell reporters such as FUCCI label cells in different phases with fluorescent protein fusions, so researchers can watch the cycle in real time. Small-molecule inhibitors, including the CDK1 inhibitor RO-3306 and palbociclib, hold cells at specific points, and CRISPR or siRNA knockdown tests what happens when a regulator disappears.\"}}]}<\/script><\/p>\n<div class=\"mbs-page\">\n<header class=\"nav\">\n<div class=\"wrap\">\n<div class=\"logo\"><a href=\"https:\/\/www.mybiosource.com\/\"><img decoding=\"async\" src=\"https:\/\/cdn.mybiosource.com\/antibody-protein-elisa-kit.png\" alt=\"MyBioSource\" style=\"height:2rem;display:block;\" \/><\/a><\/div>\n<nav class=\"nav-links\"><a href=\"#what-are-cell-cycle-regulators\">Regulators<\/a><a href=\"#how-is-the-cell-cycle-regulated\">Regulation<\/a><a href=\"#cell-cycle-checkpoints\">Checkpoints<\/a><a href=\"#cell-cycle-regulators-in-cancer\">Cancer<\/a><a href=\"#faqs\">FAQ<\/a><\/nav>\n<div class=\"nav-btn-wrap\"><button class=\"nav-btn\" type=\"button\" onclick=\"document.getElementById('nav-mobile').classList.toggle('open')\" aria-label=\"Menu\">&#9776;<\/button><\/div>\n<\/div>\n<div class=\"nav-mobile\" id=\"nav-mobile\"><a href=\"#what-are-cell-cycle-regulators\">Regulators<\/a><a href=\"#how-is-the-cell-cycle-regulated\">Regulation<\/a><a href=\"#cell-cycle-checkpoints\">Checkpoints<\/a><a href=\"#cell-cycle-regulators-in-cancer\">Cancer<\/a><a href=\"#faqs\">FAQ<\/a><\/div>\n<\/header>\n<section class=\"hero\">\n<div class=\"wrap\">\n<div>\n<p class=\"eyebrow\">Cell Biology Explained<\/p>\n<h1>What Are Cell Cycle Regulators, and What Is Their Role in Cell Division?<\/h1>\n<p class=\"lead\">Cell cycle regulators are the proteins that control when a cell divides and when it waits. They act as molecular switches that drive the cell through each phase of the cycle and halt it at checkpoints when DNA is damaged or chromosomes cannot yet separate. When these switches fail, cells can divide without proper checks, which is why cell cycle regulators are central to cancer research.<\/p>\n<div class=\"meta\"><span>MyBioSource Learning Library<\/span><span>&middot;<\/span><span>Cell Biology<\/span><\/div>\n<\/div>\n<div class=\"hero-img\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/www.mybiosource.com\/learn\/wp-content\/uploads\/2026\/10\/plant-cells-mitosis-microscope-slide.jpg\" alt=\"Pink stained cells in different stages of cell division viewed under a microscope\" width=\"1200\" height=\"480\" \/><\/div>\n<\/div>\n<\/section>\n<section class=\"strip\" aria-label=\"Key takeaways\">\n<div class=\"wrap\">\n<div class=\"item\">\n<div class=\"n\">01<\/div>\n<p>Cell cycle regulators are the proteins that move a cell through G1, S, G2, and M or hold it at a checkpoint.<\/p>\n<\/div>\n<div class=\"item\">\n<div class=\"n\">02<\/div>\n<p>Cyclin-dependent kinases (CDKs) stay inactive until they bind a cyclin, and each cyclin-CDK pair drives a different transition.<\/p>\n<\/div>\n<div class=\"item\">\n<div class=\"n\">03<\/div>\n<p>Cells tune CDK activity by controlling cyclin levels and by switching CDKs on or off with phosphorylation and CDK inhibitors such as p21 and p16.<\/p>\n<\/div>\n<div class=\"item\">\n<div class=\"n\">04<\/div>\n<p>Three checkpoints stop division when conditions fall short, and the tumor suppressors p53 and Rb enforce them.<\/p>\n<\/div>\n<div class=\"item\">\n<div class=\"n\">05<\/div>\n<p>Dysregulated cell cycle control is a hallmark of cancer, and CDK4\/6 inhibitors such as palbociclib and ribociclib now treat certain breast cancers.<\/p>\n<\/div>\n<\/div>\n<\/section>\n<section class=\"section\">\n<div class=\"wrap\">\n<div class=\"section-head\">\n<h2 id=\"what-are-cell-cycle-regulators\">What Are Cell Cycle Regulators?<\/h2>\n<p>Every dividing cell must copy its DNA once and split it evenly between two daughter cells, and a network of regulatory proteins coordinates each step. That network is the cell cycle control system, and it relies on cell cycle regulators to time each phase and to check each result.<\/p>\n<\/div>\n<div class=\"prose\">\n<h3 style=\"font-size:1.25rem;font-weight:700;color:#0f172a;margin:1.5rem 0 0.5rem;\">The Four Phases of the Cell Cycle<\/h3>\n<p>The cell cycle has four phases. In the G1 phase, the cell grows and chooses between another round of division and a pause. In the S phase, the cell replicates its DNA, and our guide to <a href=\"https:\/\/www.mybiosource.com\/learn\/what-is-dna\/\">what DNA is<\/a> explains the molecule it copies. In the G2 phase, the cell prepares for mitosis. In the M phase, it divides its chromosomes and then its cytoplasm. Cells that stop dividing can leave G1 and enter a resting state, G0.<\/p>\n<\/div>\n<div class=\"picks\">\n<div class=\"pick\">\n<h3>G1 phase<\/h3>\n<p>The cell grows and chooses between another round of division and a pause.<\/p>\n<\/div>\n<div class=\"pick\" style=\"border-top-color:#16a34a;\">\n<h3>S phase<\/h3>\n<p>The cell replicates its DNA.<\/p>\n<\/div>\n<div class=\"pick\" style=\"border-top-color:#7e22ce;\">\n<h3>G2 phase<\/h3>\n<p>The cell prepares for mitosis.<\/p>\n<\/div>\n<div class=\"pick\" style=\"border-top-color:#c2410c;\">\n<h3>M phase<\/h3>\n<p>The cell divides its chromosomes and then its cytoplasm.<\/p>\n<\/div>\n<\/div>\n<div style=\"height:2rem\"><\/div>\n<div class=\"prose\">\n<h3 style=\"font-size:1.25rem;font-weight:700;color:#0f172a;margin:1.5rem 0 0.5rem;\">Cyclins and CDKs: The Core Regulators<\/h3>\n<p>Cyclin-dependent kinases (CDKs) are the catalytic engines of the cell cycle. A CDK stays inactive on its own and needs a regulatory partner, a cyclin, before it can phosphorylate target proteins. CDK levels stay fairly constant, while cyclin levels in the cell cycle rise and fall in a set pattern, so the cyclins supply the timing signal. Full activation also needs a phosphate on the CDK activation loop, which the CDK-activating kinase (CAK) adds.<\/p>\n<\/div>\n<\/div>\n<\/section>\n<section class=\"section section-dark\">\n<div class=\"wrap\">\n<div class=\"section-head\">\n<h2 id=\"how-is-the-cell-cycle-regulated\">How Is the Cell Cycle Regulated?<\/h2>\n<p>Cells control cyclin-CDK activity by changing how much cyclin is present and by changing the state of the CDK itself. Cyclin synthesis and ubiquitin-dependent destruction set the timing, while phosphorylation and CDK inhibitor proteins control when a complex can act. Researchers who study cell cycle regulation often work with antibodies and recombinant proteins. Our <a href=\"https:\/\/www.mybiosource.com\/products-by-pathway\">products by pathway<\/a> page groups research reagents by the pathway they belong to.<\/p>\n<\/div>\n<div class=\"tools\">\n<div class=\"img\"><img decoding=\"async\" src=\"https:\/\/www.mybiosource.com\/learn\/wp-content\/uploads\/2026\/10\/cell-division-stages-chromosomes-illustration.jpg\" alt=\"Illustration of cells in stages of division showing chromosomes separating into two new cells\" width=\"1200\" height=\"800\" loading=\"lazy\" \/><\/div>\n<div class=\"tile featured span2\">\n<h3>Four Cyclin-CDK Complexes Drive the Main Transitions<\/h3>\n<p>Cyclin D with CDK4 and CDK6 responds to growth signals in G1 and starts phosphorylating the retinoblastoma protein (Rb).<\/p>\n<p>Cyclin E with CDK2 peaks at the G1\/S boundary and commits the cell to DNA replication.<\/p>\n<p>Cyclin A with CDK2 drives DNA replication during the S phase.<\/p>\n<p>Cyclin B with CDK1 triggers entry into mitosis at the G2\/M boundary.<\/p>\n<\/div>\n<div class=\"tile\">\n<h3>Cyclin Synthesis and Ubiquitin-Dependent Destruction<\/h3>\n<p>Cells make each cyclin only at the point in the cycle where it is needed and destroy it when its job ends. Ubiquitin ligases tag cyclins for destruction by the proteasome. The anaphase-promoting complex\/cyclosome (APC\/C) targets cyclin B near the end of mitosis, which switches off CDK1 and lets the cell exit mitosis. The SCF complex marks other regulators, including cyclin E and the CDK inhibitor p27, for degradation during G1 and S.<\/p>\n<\/div>\n<div class=\"tile\">\n<h3>Activating and Inhibitory Phosphorylation<\/h3>\n<p>Phosphate groups act as switches on the CDK itself. The kinase Wee1 adds inhibitory phosphates to CDK1 near its ATP-binding site, which keeps cyclin B-CDK1 inactive even after the two proteins pair. The phosphatase CDC25 removes those phosphates, releasing CDK1 to act. Together, Wee1 and CDC25 set the timing of mitotic entry, and DNA damage signals shut CDC25 down.<\/p>\n<\/div>\n<div class=\"tile\">\n<h3>CDK Inhibitor Proteins<\/h3>\n<p>CDK inhibitors are small proteins that bind CDKs or cyclin-CDK complexes and block their activity. The Cip\/Kip family, which includes p21 and p27, inhibits a broad group of cyclin-CDK complexes. The INK4 family, which includes p16, specifically binds CDK4 and CDK6 and prevents them from associating with cyclin D. DNA damage increases p21 through p53, and growth-inhibiting signals such as TGF-\u03b2 increase p27.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/section>\n<section class=\"section section-alt\">\n<div class=\"wrap\">\n<div class=\"section-head\">\n<h2 id=\"cell-cycle-checkpoints\">Cell Cycle Checkpoints and Tumor Suppressors<\/h2>\n<p>Cell cycle checkpoints are control points where the cell tests its own condition before it moves on. If a test fails, regulators block the relevant cyclin-CDK complex, and the cell waits until it repairs the problem or triggers cell death. Three major checkpoints guard the cycle.<\/p>\n<\/div>\n<div class=\"timeline\">\n<div class=\"tl-item\" data-n=\"1\">\n<h3>The G1\/S Restriction Point<\/h3>\n<p>Late in G1, the restriction point decides if a cell commits to another round of division. Before this point, the cell needs growth signals to keep going. Cyclin D-CDK4\/6 and then cyclin E-CDK2 phosphorylate Rb, which releases the E2F transcription factors that switch on genes for DNA replication. After that switch flips, the cell proceeds into the S phase even if growth signals disappear. DNA damage can also stop cells at G1\/S, because p53 raises p21, and p21 inhibits cyclin E-CDK2.<\/p>\n<\/div>\n<div class=\"tl-item\" data-n=\"2\">\n<h3>The G2\/M DNA Damage Checkpoint<\/h3>\n<p>Before mitosis, the cell checks that it has fully and accurately copied its DNA. Damaged DNA activates the kinases ATM and ATR, which in turn activate Chk2 and Chk1. Those kinases inhibit CDC25, so cyclin B-CDK1 stays inactive and mitosis cannot begin. p53 and p21 help maintain the arrest.<\/p>\n<\/div>\n<div class=\"tl-item\" data-n=\"3\">\n<h3>The Spindle Assembly Checkpoint<\/h3>\n<p>During mitosis, the spindle assembly checkpoint confirms that every chromosome attaches correctly to the spindle. A kinetochore without an attached spindle fiber produces a signal that inhibits the APC\/C. With the APC\/C blocked, cyclin B and securin stay intact, and sister chromatids stay together until every chromosome is in place.<\/p>\n<\/div>\n<\/div>\n<div class=\"prose\">\n<h3 style=\"font-size:1.25rem;font-weight:700;color:#0f172a;margin:1.5rem 0 0.5rem;\">p53 and Rb: Tumor Suppressors That Enforce the Checkpoints<\/h3>\n<p>The tumor suppressors p53 and Rb enforce several of these decisions. p53 accumulates when a cell detects DNA damage and activates genes such as p21 that halt the cycle. If the damage is too severe, p53 can also trigger apoptosis. Rb holds E2F in check until cyclin-CDK complexes phosphorylate it, so Rb acts as the gate at the restriction point.<\/p>\n<\/div>\n<\/div>\n<\/section>\n<section class=\"section\">\n<div class=\"wrap\">\n<div class=\"section-head\">\n<h2 id=\"cell-cycle-regulators-in-cancer\">Cell Cycle Regulators in Cancer<\/h2>\n<p>Cell cycle regulators keep cell division under tight control, which makes them frequent targets of the changes that lead to cancer. Tumors almost always disable at least one of these controls, and that loss lets cells divide without the usual checks.<\/p>\n<\/div>\n<div class=\"flow\">\n<div class=\"flow-step\">\n<p class=\"step\">Part 1<\/p>\n<h3>Dysregulation as a Hallmark of Cancer<\/h3>\n<p>TP53, the gene that encodes p53, carries mutations in about half of human tumors, more than any other cancer gene. Other tumors lose p16 or Rb, or they overproduce cyclin D, and each change removes a brake on the G1\/S transition.<\/p>\n<\/div>\n<div class=\"flow-arrow\">&rarr;<\/div>\n<div class=\"flow-step\">\n<p class=\"step\">Part 2<\/p>\n<h3>CDK Inhibitors as Cancer Therapeutics<\/h3>\n<p>Many tumors depend on cyclin D-CDK4\/6 activity to drive division, so drug developers built small-molecule CDK inhibitors targeting CDK4 and CDK6. Palbociclib and ribociclib block these kinases, so Rb stays unphosphorylated and cells stay in G1. Abemaciclib works the same way. The FDA approved palbociclib in 2015, and these drugs now treat hormone receptor-positive, HER2-negative breast cancer, usually alongside endocrine therapy. They work only in cells that still have functional Rb.<\/p>\n<\/div>\n<div class=\"flow-arrow\">&rarr;<\/div>\n<div class=\"flow-step\">\n<p class=\"step\">Part 3<\/p>\n<h3>Research Tools for Cell Cycle Studies<\/h3>\n<p>Researchers who study cell cycle regulators need reagents that detect and manipulate these proteins. Our <a href=\"https:\/\/www.mybiosource.com\/monoclonal\">monoclonal antibodies<\/a> and <a href=\"https:\/\/www.mybiosource.com\/polyclonal\">polyclonal antibodies<\/a> detect targets such as p53 and the CDKs, while our <a href=\"https:\/\/www.mybiosource.com\/elisa-kits\">ELISA kits<\/a> quantify them in samples. Our <a href=\"https:\/\/www.mybiosource.com\/rec-purified-protein\">recombinant and purified proteins<\/a> serve as standards and as substrates for kinase assays, and our <a href=\"https:\/\/www.mybiosource.com\/sirna\">siRNA<\/a> products allow gene knockdown studies.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/section>\n<section class=\"cta\">\n<div class=\"wrap\">\n<div>\n<h2>Find Research Reagents for Your Cell Cycle Studies<\/h2>\n<p>Studying checkpoints or CDK signaling? Browse our ELISA kits, or search our siRNA catalog for your target gene.<\/p>\n<\/div>\n<div class=\"btns\"><a class=\"primary\" href=\"https:\/\/www.mybiosource.com\/contact-us\">Contact Us<\/a><a class=\"ghost\" href=\"https:\/\/www.mybiosource.com\/elisa-kits\" target=\"_blank\" rel=\"noopener noreferrer\">Browse ELISA Kits<\/a><a class=\"ghost\" href=\"https:\/\/www.mybiosource.com\/sirna\" target=\"_blank\" rel=\"noopener noreferrer\">Browse siRNA<\/a><\/div>\n<\/div>\n<\/section>\n<section class=\"section\">\n<div class=\"wrap\">\n<div class=\"section-head\">\n<h2 id=\"faqs\">Frequently Asked Questions About Cell Cycle Regulators<\/h2>\n<\/div>\n<div class=\"faq-grid\">\n<div class=\"faq-item\">\n<h3><span>Q<\/span>What happens when cell cycle regulators malfunction?<\/h3>\n<p>When cell cycle regulators malfunction, cells either divide without proper checks or stall when they should keep dividing. The loss of a checkpoint lets cells with damaged DNA or misaligned chromosomes continue, which produces mutations and abnormal chromosome numbers (aneuploidy). Inherited mutations show the effect clearly: a faulty RB1 gene causes hereditary retinoblastoma, and a faulty TP53 gene causes Li-Fraumeni syndrome, which raises lifetime cancer risk. The opposite problem also occurs, because excess checkpoint signaling can push cells into senescence, a permanent arrest linked to tissue aging.<\/p>\n<\/div>\n<div class=\"faq-item\">\n<h3><span>Q<\/span>What is the restriction point, and why is it important?<\/h3>\n<p>The restriction point is the late G1 transition, after which a cell commits to dividing even if growth signals disappear. Arthur Pardee described it in 1974 after observing that mammalian cells deprived of growth factors stopped in G1, while cells past that point finished the cycle. The restriction point is important because it separates a reversible decision from an irreversible one: Rb phosphorylation flips a switch that makes E2F-driven gene expression self-sustaining. Cancer cells often bypass the need for growth signals, and their dependence on cyclin D-CDK4\/6 helps explain why CDK4\/6 inhibitors are effective.<\/p>\n<\/div>\n<div class=\"faq-item\">\n<h3><span>Q<\/span>What research tools are used to study cell cycle regulators?<\/h3>\n<p>Researchers measure how many cells are in each phase using flow cytometry, which measures DNA content with a fluorescent dye such as propidium iodide. EdU or BrdU incorporation labels cells in S phase, and phospho-histone H3 staining marks mitotic cells. Synchronization lets researchers study a single phase: a double thymidine block arrests cells at the G1\/S boundary, and nocodazole arrests them in mitosis. Western blotting tracks cyclin levels and Rb phosphorylation, and in vitro kinase assays measure CDK activity directly. Live-cell reporters such as FUCCI label cells in different phases with fluorescent protein fusions, so researchers can watch the cycle in real time. Small-molecule inhibitors, including the CDK1 inhibitor RO-3306 and palbociclib, hold cells at specific points, and CRISPR or siRNA knockdown tests what happens when a regulator disappears.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/section>\n<section class=\"section section-alt\" style=\"padding-top:3rem;padding-bottom:3rem;\">\n<div class=\"wrap\">\n<div class=\"section-head\" style=\"margin-bottom:1.25rem;\">\n<h2 style=\"font-size:1.25rem;\">Related Articles<\/h2>\n<\/div>\n<div class=\"related\"><a href=\"https:\/\/www.mybiosource.com\/learn\/elisa-testing\/\"><span class=\"txt\"><b>The Ultimate Guide to ELISA Testing<\/b><span>Learn how the ELISA workflow runs, which formats exist, and how to read the results.<\/span><\/span><i>&rarr;<\/i><\/a><a href=\"https:\/\/www.mybiosource.com\/learn\/westernblotting\/\"><span class=\"txt\"><b>Western Blotting<\/b><span>Discover how western blotting detects proteins and their modifications, from sample prep to quantification.<\/span><\/span><i>&rarr;<\/i><\/a><a href=\"https:\/\/www.mybiosource.com\/learn\/guide-understanding-crispr-gene-editing\/\"><span class=\"txt\"><b>A Complete Guide To Understanding CRISPR &amp; Gene Editing<\/b><span>Explore how CRISPR-Cas9 works and where researchers use gene editing.<\/span><\/span><i>&rarr;<\/i><\/a><\/div>\n<\/div>\n<\/section>\n<footer class=\"site-footer\">\n<div class=\"wrap\">\n<div>\n<div class=\"logo\"><img decoding=\"async\" src=\"https:\/\/cdn.mybiosource.com\/antibody-protein-elisa-kit.png\" alt=\"MyBioSource\" style=\"height:2rem;margin-bottom:1rem;\" \/><\/div>\n<p>Your trusted partner in life science research. 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All rights reserved. | Educational Resource<\/div>\n<\/footer>\n<p><script>document.querySelectorAll(\".nav-mobile a\").forEach(function(a){a.addEventListener(\"click\",function(){document.getElementById(\"nav-mobile\").classList.remove(\"open\");});});<\/script><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Learn what cell cycle regulators are and how cyclins and CDKs drive cell division. See how checkpoints and CDK inhibitors apply to cancer research.<\/p>\n","protected":false},"author":16,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-template-blank.php","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":""},"class_list":["post-9788","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www.mybiosource.com\/learn\/wp-json\/wp\/v2\/pages\/9788","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.mybiosource.com\/learn\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.mybiosource.com\/learn\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.mybiosource.com\/learn\/wp-json\/wp\/v2\/users\/16"}],"replies":[{"embeddable":true,"href":"https:\/\/www.mybiosource.com\/learn\/wp-json\/wp\/v2\/comments?post=9788"}],"version-history":[{"count":1,"href":"https:\/\/www.mybiosource.com\/learn\/wp-json\/wp\/v2\/pages\/9788\/revisions"}],"predecessor-version":[{"id":9791,"href":"https:\/\/www.mybiosource.com\/learn\/wp-json\/wp\/v2\/pages\/9788\/revisions\/9791"}],"wp:attachment":[{"href":"https:\/\/www.mybiosource.com\/learn\/wp-json\/wp\/v2\/media?parent=9788"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}