Create mode – the default mode when you create a requisition and PunchOut to Bio-Rad. You can create and edit multiple shopping carts
Edit mode – allows you to edit or modify an existing requisition (prior to submitting). You will be able to modify only the cart that you have PunchedOut to, and won't have access to any other carts
Inspect mode – when you PunchOut to Bio-Rad from a previously created requisition but without initiating an Edit session, you will be in this mode. You cannot modify any Cart contents
Bio-Rad-Antibodies.com relies on third-party cookies to show you pricing, allow you to order online, and connect you to My Bio-Rad. Please amend your browser settings to enable third-party cookies and access this website’s full functionality.
Click here to find out how
Dendritic cells (DCs) are a functionally, developmentally and phenotypically diverse group of cells. In addition to being potent stimulators/activators of an adaptive immune response DCs can also initiate an innate immune response and even have a role in immune tolerance (Schraml & Sousa 2015). DCs have been found to be involved in two types of immune suppression; either “central tolerance” where self-reactive T cells, direct from the thymus, are eliminated or “peripheral tolerance” where harmful antigens in the tissue are removed (Chung et al. 2013).
Classical DCs (cDCs) and pre-plasmacytoid DCs (pDCs) are derived from the common lymphoid progenitor (CLP) and common myeloid (CMP) pathways that originate in bone marrow and terminate as blood borne monocytes that develop into mature DCs. The precise point at which the development of the long lasting pDCs and the shorter lasting, high turnover, cDCs diverge remains a point of debate. More recent evidence has indicated that development may involve a common DC precursor from which cDCs are developed and a pre-plasmacytoid DCs which differentiate into plasmacytoid DCs (pDCs) (Reizis et al. 2011, Schraml & Sousa 2015).
cDCs are highly migratory and are found at sites of likely microbial encounters such as the gut, skin and lungs. The immature cDCs capture and process antigen then transit from these tissues to lymphoid organs such as spleen and lymph nodes where they mature, up-regulate co-stimulatory molecules and present the antigen in the context of a MHC-II-peptide complex to lymphocytes (Geissmann et al. 2010).
pDCs are also found in peripheral organs, primarily those of the lymphatic system in a steady state (Geissmann et al. 2010). The fundamental function of pDCs is to respond to viral infection, by the secretion of type I interferon alpha/beta; however they can also be involved in both the activation and control of T cell responses (Geissmann et al. 2010).
To date, no single cell marker has been found to be expressed exclusively on DCs, therefore a combination of the presence and absence of various cell markers can be used to identify the DCs. The table below lists key markers that can be used in the identification of DCs alongside the absence of lineage markers, such as CD3 (T cell), CD14 (monocyte), CD19 (B cell), CD56 (NK cell) and CD66b (granulocyte).
Table constructed using data from Geissmann et al. 2010, Reizis et al. 2011, Merad et al. 2013 and Schraml & Sousa 2015.
For a full list of all Dendritic Cell markers available click here