{"id":109101,"date":"2025-12-25T13:13:35","date_gmt":"2025-12-25T13:13:35","guid":{"rendered":"https:\/\/advbiomart.sytech.site\/product\/recombinant-human-conserved-oligomeric-golgi-complex-subunit-5-cog5-tuncated-acp01712\/"},"modified":"2025-12-25T13:13:36","modified_gmt":"2025-12-25T13:13:36","slug":"recombinant-human-conserved-oligomeric-golgi-complex-subunit-5-cog5-tuncated-acp01712","status":"publish","type":"product","link":"https:\/\/www.abtriva.com\/de\/product\/recombinant-human-conserved-oligomeric-golgi-complex-subunit-5-cog5-tuncated-acp01712\/","title":{"rendered":"Recombinant Human Conserved oligomeric Golgi complex subunit 5 (COG5), Truncated"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"<p>The recombinant Human COG5 was expressed with the amino acid range of 1-257. The theoretical molecular weight of the COG5 protein is 33.8 kDa. This COG5 protein is produced using e.coli expression system. The COG5 coding gene included the N-terminal 10xHis tag, which simplifies the detection and purification processes of the recombinant COG5 protein in following stages of expression and purification.Conserved oligomeric Golgi complex subunit 5 (COG5) is a part of the COG complex, which is involved in maintaining the structure and function of the Golgi apparatus. COG5 specifically plays a role in tethering vesicles and facilitating the intra-Golgi transport of proteins. Mutations in the COG5 gene can lead to defects in protein glycosylation and result in congenital disorders of glycosylation (CDG), affecting various physiological processes. Research areas involving COG5 include investigating its role in intracellular trafficking, glycosylation disorders, and cellular homeostasis. Understanding COG5&#8217;s functions contributes to insights into fundamental cellular processes and potential therapeutic targets for related disorders.<\/p>\n","protected":false},"featured_media":0,"comment_status":"open","ping_status":"closed","template":"","meta":{"_acf_changed":false},"product_brand":[],"product_cat":[168834,18],"product_tag":[24823],"class_list":["post-109101","product","type-product","status-publish","product_cat-proteins","product_cat-recombinant-proteins","product_tag-cog5","first","instock","shipping-taxable","product-type-simple"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.0 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Recombinant Human Conserved oligomeric Golgi complex subunit 5 (COG5), Truncated - AbTrivia<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.abtriva.com\/de\/product\/recombinant-human-conserved-oligomeric-golgi-complex-subunit-5-cog5-tuncated-acp01712\/\" \/>\n<meta property=\"og:locale\" content=\"de_DE\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Recombinant Human Conserved oligomeric Golgi complex subunit 5 (COG5), Truncated - AbTrivia\" \/>\n<meta property=\"og:description\" content=\"The recombinant Human COG5 was expressed with the amino acid range of 1-257. The theoretical molecular weight of the COG5 protein is 33.8 kDa. This COG5 protein is produced using e.coli expression system. The COG5 coding gene included the N-terminal 10xHis tag, which simplifies the detection and purification processes of the recombinant COG5 protein in following stages of expression and purification.Conserved oligomeric Golgi complex subunit 5 (COG5) is a part of the COG complex, which is involved in maintaining the structure and function of the Golgi apparatus. COG5 specifically plays a role in tethering vesicles and facilitating the intra-Golgi transport of proteins. Mutations in the COG5 gene can lead to defects in protein glycosylation and result in congenital disorders of glycosylation (CDG), affecting various physiological processes. Research areas involving COG5 include investigating its role in intracellular trafficking, glycosylation disorders, and cellular homeostasis. 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