{"product_id":"human-gamma-globulins-conjugated-to-agarose-beads","title":"Human Gamma Globulins Conjugated to Agarose Beads","description":"\u003cdiv style=\"max-width:1400px; margin:0 auto; padding:40px 20px; font-family:'Open Sans',sans-serif; font-weight:300; background:#fff; color:#333; font-size:0.95rem; box-sizing:border-box;\"\u003e\n  \u003cdiv style=\"display:flex; flex-direction:column; gap:20px;\"\u003e\n\u003ch2 style=\"margin:0; font-weight:600;\"\u003eHuman Gamma Globulins Conjugated to Agarose Beads – Catalog #B2025627\u003c\/h2\u003e\n\u003cp\u003eHuman Gamma Globulins Conjugated to Agarose Beads (Catalog #B2025627) consist of human immunoglobulin G (IgG) antibodies covalently immobilized on agarose beads, supplied as 5 mL of suspension. The agarose matrix provides a stable, inert support with large pore size and high protein binding capacity. Immobilization of gamma globulins on agarose beads enables rapid, straightforward affinity-based purification and isolation of target antigens, epitopes, and proteins that bind human antibodies.\u003c\/p\u003e\n\u003cdiv style=\"overflow-x:auto; max-width:100%; margin-bottom:20px;\"\u003e\n\u003ctable style=\"width:100%; max-width:640px; border-collapse:collapse;\"\u003e\n\u003ctbody\u003e\n\u003ctr style=\"border-bottom:1px solid #ddd;\"\u003e\n\u003ctd style=\"width:150px; padding:6px 10px 6px 0; vertical-align:top;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd style=\"padding:6px 0;\"\u003eB2025627\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr style=\"border-bottom:1px solid #ddd;\"\u003e\n\u003ctd style=\"width:150px; padding:6px 10px 6px 0; vertical-align:top;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd style=\"padding:6px 0;\"\u003eBatch dependent\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr style=\"border-bottom:1px solid #ddd;\"\u003e\n\u003ctd style=\"width:150px; padding:6px 10px 6px 0; vertical-align:top;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd style=\"padding:6px 0;\"\u003eBatch dependent\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr style=\"border-bottom:1px solid #ddd;\"\u003e\n\u003ctd style=\"width:150px; padding:6px 10px 6px 0; vertical-align:top;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd style=\"padding:6px 0;\"\u003e5 mL\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr style=\"border-bottom:1px solid #ddd;\"\u003e\n\u003ctd style=\"width:150px; padding:6px 10px 6px 0; vertical-align:top;\"\u003e\u003cstrong\u003eImmobilized ligand:\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd style=\"padding:6px 0;\"\u003eHuman gamma globulins (IgG)\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr style=\"border-bottom:1px solid #ddd;\"\u003e\n\u003ctd style=\"width:150px; padding:6px 10px 6px 0; vertical-align:top;\"\u003e\u003cstrong\u003eBead matrix:\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd style=\"padding:6px 0;\"\u003eAgarose\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr style=\"border-bottom:1px solid #ddd;\"\u003e\n\u003ctd style=\"width:150px; padding:6px 10px 6px 0; vertical-align:top;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd style=\"padding:6px 0;\"\u003eSuspension\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr style=\"border-bottom:1px solid #ddd;\"\u003e\n\u003ctd style=\"width:150px; padding:6px 10px 6px 0; vertical-align:top;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd style=\"padding:6px 0;\"\u003eAffinity purification and isolation of antibody-binding targets, immunoaffinity chromatography, antibody-based separation, protein purification, diagnostic immunoassays\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr style=\"border-bottom:1px solid #ddd;\"\u003e\n\u003ctd style=\"width:150px; padding:6px 10px 6px 0; vertical-align:top;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd style=\"padding:6px 0;\"\u003e2–8°C\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr style=\"border-bottom:1px solid #ddd;\"\u003e\n\u003ctd style=\"width:150px; padding:6px 10px 6px 0; vertical-align:top;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd style=\"padding:6px 0;\"\u003eHuman IgG agarose, human gamma globulins conjugated to agarose, immobilized human antibodies, IgG affinity beads, gamma globulin beads, human immunoglobulin G agarose, agarose-bound antibodies\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr style=\"border-bottom:1px solid #ddd;\"\u003e\n\u003ctd style=\"width:150px; padding:6px 10px 6px 0; vertical-align:top;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd style=\"padding:6px 0;\"\u003eBiotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 µm.\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\u003ch3 style=\"margin-top:30px;\"\u003eScientific Overview\u003c\/h3\u003e\n\u003cp\u003eAgarose-based affinity chromatography materials have become standard tools for rapid, high-yield purification of proteins and other biomolecules. The agarose polysaccharide matrix is chemically inert, supports large pore sizes, and tolerates a wide range of pH and ionic strength conditions. When human gamma globulins (IgG antibodies) are covalently immobilized onto agarose beads, the resulting material captures and concentrates proteins or antigens that bind human IgG, enabling straightforward affinity separation. The beads can be used in column formats, batch binding, or with automated liquid handlers for rapid sample preparation in proteomics, diagnostic development, and research applications.\u003c\/p\u003e\n\u003cp\u003eKey applications include:\u003c\/p\u003e\n\u003cul style=\"padding-left:20px;\"\u003e\n\u003cli\u003eAffinity purification of antigens and epitopes recognized by human antibodies\u003c\/li\u003e\n\u003cli\u003eEnrichment of human IgG-binding proteins for proteomic analysis\u003c\/li\u003e\n\u003cli\u003eDevelopment of immunoassays and diagnostic tests\u003c\/li\u003e\n\u003cli\u003eAntibody-based separation in bioprocess scale-up\u003c\/li\u003e\n\u003cli\u003eDepletion of human IgG-binding contaminants from samples\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 style=\"margin-top:30px;\"\u003eUsage \u0026amp; Handling Guidance\u003c\/h3\u003e\n\u003cp\u003eStore the suspension at 2–8°C. Mix gently before use. The beads can be used in column, batch, or automated formats depending on your application.\u003c\/p\u003e\n\u003cul style=\"padding-left:20px;\"\u003e\n\u003cli\u003e\n\u003cstrong\u003eBinding:\u003c\/strong\u003e Add beads to your sample and incubate at appropriate pH and temperature to allow human IgG to capture target antigens or proteins; optimize binding conditions for your specific application.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eSeparation:\u003c\/strong\u003e Centrifuge or allow beads to settle, then remove supernatant. Alternatively, use in column flow-through mode.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eWashing:\u003c\/strong\u003e Resuspend and wash beads with appropriate buffer to remove unbound material and improve purity of bound complexes.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eElution:\u003c\/strong\u003e Elute bound proteins by lowering pH, increasing salt concentration, or using competitive displacement, depending on binding strength and your downstream requirements.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 style=\"margin-top:30px;\"\u003eWhat You Get\u003c\/h3\u003e\n\u003cul style=\"padding-left:20px;\"\u003e\n\u003cli\u003e5 mL of human gamma globulin-conjugated agarose bead suspension\u003c\/li\u003e\n\u003cli\u003eReady-to-use affinity chromatography resin\u003c\/li\u003e\n\u003cli\u003eLarge bead volume for extensive affinity purification work\u003c\/li\u003e\n\u003cli\u003eFor research use only (RUO)\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 style=\"margin-top:30px;\"\u003eWhy Researchers Choose It\u003c\/h3\u003e\n\u003cul style=\"padding-left:20px;\"\u003e\n\u003cli\u003eHuman IgG immobilization allows specific capture of IgG-binding targets\u003c\/li\u003e\n\u003cli\u003eAgarose matrix is inert, chemically stable, and compatible with standard chromatography equipment\u003c\/li\u003e\n\u003cli\u003eSimple protocol: mix, bind, wash, and elute without complex chemistry or specialized apparatus\u003c\/li\u003e\n\u003cli\u003eHigh-volume package (5 mL) provides ample material for multiple purification rounds\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 style=\"margin-top:30px;\"\u003eFrequently Asked Questions (FAQ)\u003c\/h3\u003e\n\u003cul style=\"padding-left:20px;\"\u003e\n\u003cli\u003e\n\u003cstrong\u003eWhat proteins can I purify with these beads?\u003c\/strong\u003e\u003cbr\u003eThese beads capture antigens, epitopes, and proteins that bind human immunoglobulin G. Optimize your binding conditions for your specific target.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eHow do I elute bound material?\u003c\/strong\u003e\u003cbr\u003eElution depends on the strength of the IgG-antigen interaction. Try pH changes (0.1 M glycine–HCl, pH 2.5–3.0), increased salt, or mild detergents. Request the COA or contact us for optimization guidance.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eCan I reuse these beads?\u003c\/strong\u003e\u003cbr\u003eYes. After elution, regenerate beads by washing with neutral buffer and storing at 2–8°C. Reusability depends on the strength of your elution conditions; request lot documentation for regeneration protocols.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eHow should I store them?\u003c\/strong\u003e\u003cbr\u003eKeep at 2–8°C. Gently mix before use to ensure even suspension.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eCan I get a COA or technical data?\u003c\/strong\u003e\u003cbr\u003eYes. Request a quote or contact us and we will provide available lot documentation including ligand density and binding capacity data.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cdiv style=\"margin-top:20px; font-weight:bold; color:#c8102e;\"\u003eThis product is for Research Use Only (RUO). It is not intended for diagnostic or therapeutic use in humans or animals.\u003c\/div\u003e\n\u003chr\u003e\n\u003ch4\u003eReferences\u003c\/h4\u003e\n\u003cul style=\"padding-left:0; margin:0; list-style:none;\"\u003e\n\u003cli style=\"display:flex; justify-content:space-between; align-items:flex-start; gap:12px; padding:8px 0; border-bottom:1px solid #eee;\"\u003e\n\u003cspan style=\"flex:1;\"\u003eGrodzki AC, Berenstein E. Antibody purification: affinity chromatography - protein A and protein G Sepharose. \u003cem\u003eMethods Mol Biol.\u003c\/em\u003e 2010;588:33-41.\u003c\/span\u003e\u003ca href=\"https:\/\/doi.org\/10.1007\/978-1-59745-324-0_5\" target=\"_blank\" rel=\"noopener\" style=\"flex-shrink:0; margin-top:2px;\"\u003e\u003cimg src=\"https:\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/Reference.png?v=1775409336\" alt=\"Reference\" style=\"height:28px; width:auto;\"\u003e\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli style=\"display:flex; justify-content:space-between; align-items:flex-start; gap:12px; padding:8px 0; border-bottom:1px solid #eee;\"\u003e\n\u003cspan style=\"flex:1;\"\u003eKnödler M, Rühl C, Opdensteinen P, Buyel JF. Activated Cross-linked Agarose for the Rapid Development of Affinity Chromatography Resins - Antibody Capture as a Case Study. \u003cem\u003eJ Vis Exp.\u003c\/em\u003e 2019;(150).\u003c\/span\u003e\u003ca href=\"https:\/\/doi.org\/10.3791\/59933\" target=\"_blank\" rel=\"noopener\" style=\"flex-shrink:0; margin-top:2px;\"\u003e\u003cimg src=\"https:\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/Reference.png?v=1775409336\" alt=\"Reference\" style=\"height:28px; width:auto;\"\u003e\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli style=\"display:flex; justify-content:space-between; align-items:flex-start; gap:12px; padding:8px 0; border-bottom:1px solid #eee;\"\u003e\n\u003cspan style=\"flex:1;\"\u003eHnasko RM, McGarvey JA. Affinity Purification of Antibodies. \u003cem\u003eMethods Mol Biol.\u003c\/em\u003e 2015;1318:29-41.\u003c\/span\u003e\u003ca href=\"https:\/\/doi.org\/10.1007\/978-1-4939-2742-5_3\" target=\"_blank\" rel=\"noopener\" style=\"flex-shrink:0; margin-top:2px;\"\u003e\u003cimg src=\"https:\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/Reference.png?v=1775409336\" alt=\"Reference\" style=\"height:28px; width:auto;\"\u003e\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli style=\"display:flex; justify-content:space-between; align-items:flex-start; gap:12px; padding:8px 0; border-bottom:1px solid #eee;\"\u003e\n\u003cspan style=\"flex:1;\"\u003eChen C, Huang QL, Jiang SH, Pan X, Hua ZC. Immobilized protein ZZ, an affinity tool for immunoglobulin isolation and immunological experimentation. \u003cem\u003eBiotechnol Appl Biochem.\u003c\/em\u003e 2006;45(Pt 2):87-92.\u003c\/span\u003e\u003ca href=\"https:\/\/doi.org\/10.1042\/BA20060055\" target=\"_blank\" rel=\"noopener\" style=\"flex-shrink:0; margin-top:2px;\"\u003e\u003cimg src=\"https:\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/Reference.png?v=1775409336\" alt=\"Reference\" style=\"height:28px; width:auto;\"\u003e\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n  \u003c\/div\u003e\n\u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":52813632504106,"sku":"BTS-B2025627","price":2005.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2025627.png?v=1790900006","url":"https:\/\/bluetigerscientific.com\/products\/human-gamma-globulins-conjugated-to-agarose-beads","provider":"Blue Tiger Scientific","version":"1.0","type":"link"}