{"product_id":"abcam-ab184178","title":"Abcam, ab184178, Anti-TPGS1 antibody [EPR14324]","description":"\u003cp\u003eSize: 100µL \/ 1mL\u003cbr\u003e\nRabbit Recombinant Monoclonal TPGS1 antibody. Suitable for IP, WB, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples. Cited in 4 publications.\u003cbr\u003e\nKey facts\u003cbr\u003e\nHost species:Rabbit,\u003cbr\u003e\nClonality:Monoclonal,\u003cbr\u003e\nClone number:EPR14324,\u003cbr\u003e\nIsotype:IgG,\u003cbr\u003e\nCarrier free:No,\u003cbr\u003e\nReacts with:Mouse, Rat, Human,\u003cbr\u003e\nApplications:IP, WB, Flow Cyt (Intra)See reactivity dataSee the reactivity data table below for information on validated species and application combinations.,\u003cbr\u003e\nImmunogen:The exact immunogen used to generate this antibody is proprietary information.\u003c\/p\u003e\n\n\u003cp\u003eProduct details:\u003cbr\u003e\nPatented technology\u003cbr\u003e\nOur RabMAb\u003cbr\u003e\ntechnology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to\u003cbr\u003e\nRabMAb® patents\u003cbr\u003e\nWhat are the advantages of a recombinant monoclonal antibody?\u003cbr\u003e\nThis product is a recombinant monoclonal antibody, which offers several advantages including:\u003cbr\u003e\n- High batch-to-batch consistency and reproducibility\u003cbr\u003e\n- Improved sensitivity and specificity\u003cbr\u003e\n- Long-term security of supply\u003cbr\u003e\n- Animal-free batch production\u003cbr\u003e\nFor more information, read more on\u003cbr\u003e\nrecombinant antibodies\u003c\/p\u003e\n\n\u003cp\u003eProperties and Storage Information:\u003cbr\u003e\nForm-Liquid, Purity-Tissue culture supernatant, Storage buffer-pH: 7.2Preservative: 0.01% Sodium azideConstituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA, Shipped at conditions-Blue Ice, Appropriate short-term storage duration-1-2 weeks, Appropriate short-term storage conditions-+4°C, Appropriate long-term storage conditions--20°C, Aliquoting information-Upon delivery aliquot, Storage information-Avoid freeze \/ thaw cycle\u003c\/p\u003e\n\n\u003cp\u003eSupplementary Information:\u003cbr\u003e\nThis supplementary information is collated from multiple sources and compiled automatically.\u003cbr\u003e\nTPGS1 also known as TPR Glycosylation Sensor 1 functions primarily as a sensor and regulator of glycosylation within the cell. Its molecular mass is approximately 85 kDa and it predominantly localizes in the endoplasmic reticulum membrane where it plays an important role in monitoring N-linked glycosylation processes. TPGS1 is expressed in various tissues showing higher levels in organs like the liver and pancreas which are integral to metabolism and detoxification processes.\u003cbr\u003e\nBiological function summary\u003cbr\u003e\nThe TPGS1 protein interacts with glycoproteins to ensure correct folding and function important for maintaining cellular homeostasis. It frequently operates in association with complexes involved in protein processing particularly those related to the calnexin\/calreticulin cycle. TPGS1 contributes to quality control by detecting improperly glycosylated proteins directing them for degradation to prevent accumulation of defective proteins which could disrupt cellular function.\u003cbr\u003e\nPathways\u003cbr\u003e\nTPGS1 plays important roles in the unfolded protein response (UPR) and the endoplasmic reticulum-associated degradation (ERAD) pathways. Within these pathways TPGS1 works closely with proteins such as BiP\/GRP78 and EDEM which facilitate the identification and disposal of misfolded glycoproteins. By modulating protein folding and degradation TPGS1 helps maintain ER function and prevent stress conditions that could affect the entire cellular network.\u003cbr\u003e\nTPGS1 has connections with neurodegenerative diseases and congenital disorders of glycosylation. Mismanagement of glycoproteins due to TPGS1 malfunction can contribute to neurodegenerative conditions where protein aggregation becomes problematic. In congenital glycosylation disorders TPGS1’s interaction with proteins like TMEM165 may lead to incorrect glycosylation patterns resulting in varied systemic symptoms. Understanding TPGS1’s role in these pathological conditions may aid in developing potential therapeutic strategies.\u003c\/p\u003e","brand":"Abcam","offers":[{"title":"Default Title","offer_id":46850330001577,"sku":"ab184178","price":0.99,"currency_code":"USD","in_stock":true}],"url":"https:\/\/iright.com\/products\/abcam-ab184178","provider":"Iright","version":"1.0","type":"link"}