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DOK proteins are enzymatically inert adaptor or scaffolding proteins. Additionally we are shipping DOK3 Antibodies (93) and DOK3 Proteins (8) and many more products for this protein.
DOK2 and DOK3 expression was significantly reduced in HTLV-1-infected T cells.
The Dok-3/Grb2 (show GRB2 ELISA Kits) protein signal module attenuates Lyn (show LYN ELISA Kits) kinase-dependent activation of Syk (show SYK ELISA Kits) kinase in B cell antigen receptor microclusters
absence of DOK3 increases LPS (show IRF6 ELISA Kits) signaling, contributing to LPS (show IRF6 ELISA Kits)-induced tolerance. Thus, DOK3 plays a role in TLR signaling during both naive and endotoxin-induced tolerant conditions
The novel platelet adapter Dok-3 is tyrosine phosphorylated in an Src kinase (show CSK ELISA Kits)-independent manner downstream of alphaIIbbeta3 in human platelets, leading to an interaction with Grb2 (show GRB2 ELISA Kits) and SHIP-1 (show INPP5D ELISA Kits).
findings indicate that Dok-3 sequesters Grb2 (show GRB2 ELISA Kits) from Shc (show SHC1 ELISA Kits) and inhibits the Ras-Erk (show EPHB2 ELISA Kits) pathway downstream of PTKs
we demonstrate that CpG treatment leads to ubiquitin-mediated degradation of DOK3 via interaction with an E3 ligase TNFR (show TNFRSF1A ELISA Kits)-associated factor 6 (TRAF6 (show TRAF6 ELISA Kits)).
This study reveals DOK3 as a nonredundant regulator of plasma cell differentiation by up-regulating PD-1 (show PDCD1 ELISA Kits) ligand expression through the attenuation of calcium signaling.
Data show that docking protein 3 (DOK3) plays a role in TLR3 (show TLR3 ELISA Kits) signaling by enabling TNFR (show TNFRSF1A ELISA Kits)-associated factor (TRAF) 3 (show TRAF3 ELISA Kits)/TANK-binding kinase (TBK) 1 (show TBK1 ELISA Kits) binding and facilitating TBK1 (show TBK1 ELISA Kits) and IFN regulatory factor 3 activation and the induction of IFN-beta (show IFNB1 ELISA Kits) production.
DOK3 physically associated with the ITAM of DAP12 (show TYROBP ELISA Kits) through its phosphotyrosine-binding domain. In response to LPS (show TLR4 ELISA Kits), DOK3 was phosphorylated in a DAP12 (show TYROBP ELISA Kits)- and Src (show SRC ELISA Kits)-dependent manner, which led to translocation of phosphorylated DOK3 to the plasma membrane.
Triple Dok1 (show DOK1 ELISA Kits) Doc2 (show DOC2A ELISA Kits) Doc3 knockout leads to spontaneous pulmonary inflammation with hallmarks of asthma.
absence of DOK3 increases LPS (show TLR4 ELISA Kits) signaling, contributing to LPS (show TLR4 ELISA Kits)-induced tolerance. Thus, DOK3 plays a role in TLR signaling during both naive and endotoxin-induced tolerant conditions
identify a surprising but pivotal role for dynein and the microtubule network alongside Grb2 (show GRB2 ELISA Kits), Dok-3, and Cbl (show CBL ELISA Kits) in antigen gathering during B cell activation (show BLNK ELISA Kits)
Subcellular localization of Grb2 (show GRB2 ELISA Kits) by the adaptor protein Dok-3 restricts the intensity of Ca2 (show CA2 ELISA Kits)+ signaling in B cells.
In the absence of Dok-3, the localization of the inhibitory phosphatase SHIP-1 (show INPP5D ELISA Kits) to the plasma membrane is intact while its phosphorylation is compromised, suggesting that Dok-3 could function to facilitate or sustain the activation of SHIP-1 (show INPP5D ELISA Kits).
DOK proteins are enzymatically inert adaptor or scaffolding proteins. They provide a docking platform for the assembly of multimolecular signaling complexes. Plays a role as negative regulator of the mobilization of calcium ions and of calcium signaling.
docking protein 3
, Dok-like protein
, downstream of tyrosine kinase 3
, p62(dok)-like protein
, p62Dok-like protein
, Downstream of tyrosine kinase 3