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anti-Mouse (Murine) LCP2 Antikörper:
anti-Rat (Rattus) LCP2 Antikörper:
anti-Human LCP2 Antikörper:
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Human Monoclonal LCP2 Primary Antibody für IF, IP - ABIN968146
Harder, Kuhn: Selective accumulation of raft-associated membrane protein LAT in T cell receptor signaling assemblies. in The Journal of cell biology 2000
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Human Monoclonal LCP2 Primary Antibody für WB - ABIN967597
Fang, Motto, Ross, Koretzky: Tyrosines 113, 128, and 145 of SLP-76 are required for optimal augmentation of NFAT promoter activity. in Journal of immunology (Baltimore, Md. : 1950) 1996
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Human Monoclonal LCP2 Primary Antibody für WB - ABIN967606
Janssen, Zhang: Adaptor proteins in lymphocyte activation. in Current opinion in immunology 2003
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Human Monoclonal LCP2 Primary Antibody für ICS - ABIN1177174
Wu, Koretzky: The SLP-76 family of adapter proteins. in Seminars in immunology 2004
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Human Monoclonal LCP2 Primary Antibody für IP, WB - ABIN2476521
Sarrafian: Fasciotomy of the foot: an anatomical study with special reference to release of the calcaneal compartment. in Foot & ankle 1990
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Human Monoclonal LCP2 Primary Antibody für ICS - ABIN1176934
Bonilla, Fujita, Pivniouk, Chan, Geha: Adapter proteins SLP-76 and BLNK both are expressed by murine macrophages and are linked to signaling via Fcgamma receptors I and II/III. in Proceedings of the National Academy of Sciences of the United States of America 2000
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Human Polyclonal LCP2 Primary Antibody für IHC, ELISA - ABIN1532089
Tomomura, Hasegawa, Suda, Sakagami, Tomomura et al.: Serum calcium-decreasing factor, caldecrin, inhibits receptor activator of NF-?B ligand (RANKL)-mediated Ca2+ signaling and actin ring formation in mature osteoclasts via suppression of Src signaling ... in The Journal of biological chemistry 2012
Human Monoclonal LCP2 Primary Antibody für ICS - ABIN1176936
Bubeck Wardenburg, Fu, Jackman, Flotow, Wilkinson, Williams, Johnson, Kong, Chan, Findell: Phosphorylation of SLP-76 by the ZAP-70 protein-tyrosine kinase is required for T-cell receptor function. in The Journal of biological chemistry 1996
Biochemical analyses revealed that mutant T cells were hypersensitive to TCR stimulation. Indeed, phosphorylation of several signaling proteins, including SLP76 itself, phospholipase Cgamma1 and the protein kinases AKT and ERK1/2, was increased
slp-76 contributes to the regulation of the tissue distribution, PLZF (zeige ZBTB16 Antikörper), and cytokine expression of iNKT cells via ADAP (zeige APP Antikörper)-dependent and -independent mechanisms.
findings identify ACK1 (zeige TNK2 Antikörper) as a novel SLP-76-associated protein-tyrosine kinase (zeige YES1 Antikörper) that modulates early activation events in T cells.
immune cell adaptor SLP-76 binds directly to SUMO-RanGAP1 (zeige RANGAP1 Antikörper) of cytoplasmic fibrils of the nuclear pore complex, and this interaction is needed for optimal NFATc1 (zeige NFATC1 Antikörper) and NF-kappaB (zeige NFKB1 Antikörper) p65 (zeige NFkBP65 Antikörper) nuclear entry in T cells
these studies establish Slp-76 as a critical determinant of NK-cell development and NK cell mediated elimination of missing-self target cells in mice
Data show that a splice variant of SLP-76 signal transducing adaptor protein (SLP-76 or Lcp2) reduced the amount of SLP-76 protein by ~90%, disrupting immunogenic and tolerogenic pathways to different degrees.
this analysis identified 65 proteins not associated before with the Zap70 (zeige ZAP70 Antikörper)-Lat (zeige LAT Antikörper)-SLP-76 network and thus should provide cues for future functional experiments.
A yopH mutant survived better in the absence of neutrophils, indicating that neutrophil inactivation by YopH by targeting PRAM-1 (zeige PRAM1 Antikörper)/SKAP-HOM (zeige SKAP2 Antikörper) and SLP-76/Vav (zeige VAV1 Antikörper)/PLCgamma2 (zeige PLCG2 Antikörper) signaling hubs may be critical for Yersinia survival.
analysis of a costimulatory mechanism by which CXCL12 (zeige CXCL12 Antikörper) and antigen converge at SLP-76 microcluster formation to enhance T cell responses
Findings indicate that SLP-76 is an essential signaling component for basophil activation downstream of both FcepsilonRI (zeige FCER1A Antikörper) and the IL-3 (zeige IL-3 Antikörper) receptor.
These data are consistent with a model in which bivalent recruitment of a GADS (zeige GRAP2 Antikörper)/SLP-76 complex is required for costimulation by CD6 (zeige CD6 Antikörper).
LAT (zeige ORC3 Antikörper) and SLP-76 are randomly dispersed throughout the clusters that form upon T cell receptor engagement.
SLP76 is ectopically expressed in chronic lymphocytic leukemia cells where it plays a role in B-cell receptor signaling.
findings identify ACK1 (zeige TNK2 Antikörper) as a novel SLP-76-associated protein-tyrosine kinase (zeige EPHA8 Antikörper) that modulates early activation events in T cells.
Data strongly suggest that chemokine-stimulated associations between Vav1, SLP-76, and ADAP facilitate Rac1 activation and alpha4beta1-mediated adhesion, whereas Pyk2 opposes this adhesion by limiting Rac1 activation.
TSAD (zeige SH2D2A Antikörper) binds to and co-localizes with Nck (zeige NCK1 Antikörper). Expression of TSAD (zeige SH2D2A Antikörper) increases both Nck (zeige NCK1 Antikörper)-Lck (zeige LCK Antikörper) and Nck (zeige NCK1 Antikörper)-SLP-76 interaction in T cells.
immune cell adaptor SLP-76 binds directly to SUMO-RanGAP1 (zeige RANGAP1 Antikörper) of cytoplasmic fibrils of the nuclear pore complex, and this interaction is needed for optimal NFATc1 (zeige NFATC1 Antikörper) and NF-kappaB (zeige NFKB1 Antikörper) p65 (zeige GORASP1 Antikörper) nuclear entry in T cells
SLP-76 N-terminal tyrosine residues regulate a dynamic signaling equilibrium involving feedback of proximal T-cell receptor signaling
Multipoint binding of SLP-76 to ADAP (zeige FYB Antikörper) facilitates the assembly of SLP-76 microclusters.
SLP-76 was originally identified as a substrate of the ZAP-70 protein tyrosine kinase following T cell receptor (TCR) ligation in the leukemic T cell line Jurkat. The SLP-76 locus has been localized to human chromosome 5q33 and the gene structure has been partially characterized in mice. The human and murine cDNAs both encode 533 amino acid proteins that are 72% identical and comprised of three modular domains. The NH2-terminus contains an acidic region that includes a PEST domain and several tyrosine residues which are phosphorylated following TCR ligation. SLP-76 also contains a central proline-rich domain and a COOH-terminal SH2 domain. A number of additional proteins have been identified that associate with SLP-76 both constitutively and inducibly following receptor ligation, supporting the notion that SLP-76 functions as an adaptor or scaffold protein. Studies using SLP-76 deficient T cell lines or mice have provided strong evidence that SLP-76 plays a positive role in promoting T cell development and activation as well as mast cell and platelet function.
SH2 domain-containing leukocyte protein of 76 kDa
, SLP-76 tyrosine phosphoprotein
, lymphocyte cytosolic protein 2 (SH2 domain-containing leukocyte protein of 76kD)
, 76 kDa tyrosine phosphoprotein
, SH2 domain-containing leukocyte protein of 76kD
, lymphocyte cytosolic protein 2
, tyrosine phosphoprotein slp-76