{"product_id":"abcam-ab303498","title":"Abcam, ab303498, Anti-GJB2 antibody [EPR26418-19]","description":"\u003cp\u003eSize: 20µL \/ 100µL \/ 1mL\u003cbr\u003e\nRabbit Recombinant Monoclonal GJB2 antibody. Suitable for IHC-P, IHC-Fr and reacts with Mouse, Rat samples.\u003cbr\u003e\nKey facts\u003cbr\u003e\nHost species:Rabbit,\u003cbr\u003e\nClonality:Monoclonal,\u003cbr\u003e\nClone number:EPR26418-19,\u003cbr\u003e\nIsotype:IgG,\u003cbr\u003e\nCarrier free:No,\u003cbr\u003e\nReacts with:Mouse, Rat,\u003cbr\u003e\nApplications:IHC-Fr, IHC-PSee 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, Purification technique-Affinity purification Protein A, Storage buffer-pH: 7.2 - 7.4Preservative: 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\nGJB2 also known as Connexin 26 is a protein that forms part of gap junctions and is composed of a unit mass of about 26 kDa. This protein is located mainly in the cochlea within the inner ear but also shows expression in non-sensory cells of the skin kidney liver and lungs. GJB2 consists of four transmembrane domains two extracellular loops and a cytoplasmic loop. Each unit of Connexin 26 requires a total of six molecules to assemble into a structure known as a connexon which are essential for cell-to-cell communication.\u003cbr\u003e\nBiological function summary\u003cbr\u003e\nGJB2 forms channels allowing ions and small molecules to pass between cells enabling direct cell communication. This protein plays a critical role in maintaining homeostasis within tissues by mediating the transfer of signaling molecules like calcium ions and cyclic AMP. GJB2 works together with other connexins to form gap junction channels contributing to the regulation within complex tissue structures. Its role is significant in the auditory system where it facilitates the recycling of potassium ions necessary for converting sound waves into electrical signals.\u003cbr\u003e\nPathways\u003cbr\u003e\nGJB2 interacts prominently in pathways related to cellular communication and signal transduction. The gap junction network that GJB2 participates in is important for hearing involving a cascade of intercellular ionic and metabolic cooperation. Within these pathways GJB2 is functionally related to other connexin proteins like Connexin 30 which often co-localizes in the cochlea to ensure auditory function. This interconnectedness helps maintain the proper function of various epithelial tissues involved in different physiological processes.\u003cbr\u003e\nMutations in GJB2 are a common cause of non-syndromic hearing loss particularly autosomal recessive deafness. Its dysfunction can lead to improper potassium ion recycling in the cochlea leading to sensory neural hearing loss. Another condition linked to alterations in GJB2 is Keratitis-ichthyosis-deafness (KID) syndrome a rare disorder affecting the skin eyes and hearing. Mutations that disrupt GJB2 function often correlate with changes in Connexin 30 altering the balance of gap junction communication and resulting in these clinical manifestations.\u003c\/p\u003e","brand":"Abcam","offers":[{"title":"Default Title","offer_id":46850395963561,"sku":"ab303498","price":0.99,"currency_code":"USD","in_stock":true}],"url":"https:\/\/iright.com\/products\/abcam-ab303498","provider":"Iright","version":"1.0","type":"link"}