{"product_id":"abcam-ab259218","title":"Abcam, ab259218, Human TXLNA (Alpha Taxilin) knockout HeLa cell lysate","description":"\u003cp\u003eSize: 1Kit\u003cbr\u003e\nTXLNA KO cell lysate available now. KO validated by. Free of charge wild type control included. Knockout achieved by using CRISPR\/Cas9, Homozygous: 1 bp insertion in exon 2.\u003cbr\u003e\nKey facts\u003cbr\u003e\nCell type:HeLa,\u003cbr\u003e\nSpecies or organism:Human,\u003cbr\u003e\nTissue:Cervix,\u003cbr\u003e\nKnockout validation:Sanger Sequencing,\u003cbr\u003e\nMutation description:Knockout achieved by using CRISPR\/Cas9, Homozygous: 1 bp insertion in exon 2.,\u003cbr\u003e\nDisease:Adenocarcinoma\u003c\/p\u003e\n\n\u003cp\u003eProduct details:\u003cbr\u003e\nKnockout cell lysate achieved by CRISPR\/Cas9.\u003cbr\u003e\nREACH authorisation\u003cbr\u003e\nAbcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.\u003cbr\u003e\nIt is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.\u003cbr\u003e\nLysate preparation:\u003cbr\u003e\nOur lysates are made using RIPA buffer to which we add a protease inhibitor cocktail and phosphatase inhibitor cocktail (ratio: 300:100:10).\u003cbr\u003e\nThis means that the protein of interest is denatured.\u003cbr\u003e\nIf you require a native form of the protein please use the live cell version. Please refer to our lysis protocol for further details on how our lysates are prepared.\u003cbr\u003e\nUser storage instructions:\u003cbr\u003e\nLyophilizate may be stored at 4°C. After reconstitution, store at -20°C for short-term storage or -80°C for long-term storage.\u003cbr\u003e\nThis product is subject to limited use licenses from The Broad Institute, ERS Genomics Limited and Sigma-Aldrich Co. LLC, and is developed with patented technology. For full details of the licenses and patents please refer to our\u003cbr\u003e\nlimited use license\u003cbr\u003e\npatent pages\u003c\/p\u003e\n\n\u003cp\u003eProperties and Storage Information:\u003cbr\u003e\nGene name-TXLNA, Gene editing type-Knockout, Gene editing method-CRISPR technology, Knockout validation-Sanger Sequencing, Zygosity-Homozygous, Shipped at conditions-Ambient - Can Ship with Ice, Appropriate short-term storage conditions--20°C, Appropriate long-term storage conditions--20°C\u003c\/p\u003e\n\n\u003cp\u003eSupplementary Information:\u003cbr\u003e\nThis supplementary information is collated from multiple sources and compiled automatically.\u003cbr\u003e\nAlpha Taxilin also known as TXLNA taxilin alpha or IL8RA binding protein is a protein with a molecular mass of about 49 kDa. It plays a role in intracellular transport processes including vesicle fusion. Primarily expressed in the brain Alpha Taxilin interacts with membranes and cytoskeletal elements to facilitate cargo and organelle movement. Its presence in other tissues such as the placenta suggests additional roles beyond neural activities.\u003cbr\u003e\nBiological function summary\u003cbr\u003e\nThis protein mediates protein trafficking and membrane dynamics within cells. Alpha Taxilin forms part of a complex involving several SNARE proteins like syntaxins which are essential for vesicle docking and fusion. By participating in these interactions Alpha Taxilin aids in maintaining cellular homeostasis and supporting signal transduction processes.\u003cbr\u003e\nPathways\u003cbr\u003e\nAlpha Taxilin plays a role in intracellular signaling and vesicular transport processes influencing pathways such as neurotransmitter release and hormone secretion. It associates with other proteins like syntaxin 1 contributing to the protein sorting and vesicular trafficking pathway. These pathways are integral to maintaining cellular communication and proper distribution of signaling molecules.\u003cbr\u003e\nAlpha Taxilin associates with neurodevelopmental and neurodegenerative conditions. Abnormal expression levels or mutations can contribute to disorders such as schizophrenia and Alzheimer's disease. Through its interaction with SNARE proteins particularly syntaxin 1 Alpha Taxilin influences processes that when disrupted may lead to synaptic dysfunction emphasizing its potential role in nervous system disorders.\u003c\/p\u003e","brand":"Abcam","offers":[{"title":"Default Title","offer_id":46845191192745,"sku":"ab259218","price":0.99,"currency_code":"USD","in_stock":true}],"url":"https:\/\/iright.com\/ar\/products\/abcam-ab259218","provider":"Iright","version":"1.0","type":"link"}