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anti-Human Crk Antibodies:
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Chicken Monoclonal Crk Primary Antibody for BI, IP - ABIN967703
Cho, Klemke: Purification of pseudopodia from polarized cells reveals redistribution and activation of Rac through assembly of a CAS/Crk scaffold. in The Journal of cell biology 2002
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Chicken Monoclonal Crk Primary Antibody for BI, IP - ABIN967702
Fournier, Lamorte, Maroun, Lupher, Band, Langdon, Park: Cbl-transforming variants trigger a cascade of molecular alterations that lead to epithelial mesenchymal conversion. in Molecular biology of the cell 2000
Show all 7 Pubmed References
Human Monoclonal Crk Primary Antibody for ICC, FACS - ABIN969063
Watanabe, Tsuda, Tanaka, Ohba, Kawaguchi, Majima, Sawa, Minami: Adaptor protein Crk induces Src-dependent activation of p38 MAPK in regulation of synovial sarcoma cell proliferation. in Molecular cancer research : MCR 2009
Show all 2 Pubmed References
Human Monoclonal Crk Primary Antibody for ICC, FACS - ABIN969062
Tanaka: [Biological roles of signaling adaptor protein CRK]. in Seikagaku. The Journal of Japanese Biochemical Society 2009
Show all 2 Pubmed References
Human Polyclonal Crk Primary Antibody for PLA, WB - ABIN514601
Liu, Chen, Chau, Jan, Chen, Hsu, Lin, Juang, Lu, Cheng, Chen, Chang, Ting, Kao, Hsiao, Huang: Analysis of protein-protein interactions in cross-talk pathways reveals CRKL protein as a novel prognostic marker in hepatocellular carcinoma. in Molecular & cellular proteomics : MCP 2013
Human Polyclonal Crk Primary Antibody for ICC, IF - ABIN442021
Park, Choi, Choi, Kim, Kang, Jung, Lee, Kim, Freeman, Lee, Gho, Kim: Identification and characterization of proteins isolated from microvesicles derived from human lung cancer pleural effusions. in Proteomics 2013
The adaptor proteins Crk and Crk-like (Crkl (show CRKL Antibodies)), with which Dock proteins are known to interact physically, are also required for myoblast fusion.
Crk-dependent increased phosphorylation of CD3zeta coincided with inhibition of TCR downmodulation, supporting a positive role for Crk adaptor proteins in TCR-mediated signal amplification.
This mini review will focus on the emerging roles of Crk adaptors during myocardial I/R injury.
TGF-beta (show TGFB1 Antibodies) and Crk collaborate to form a positive feedback loop to facilitate epithelial-mesenchymal transition (EMT (show ITK Antibodies)).
The results suggest the involvement of Crk adaptor proteins in the early stages of T cell activation in which Crk might help recruiting effector proteins to the vicinity of the phospho-CD3zeta (show CD247 Antibodies) and contribute to the fine-tuning of the TCR/CD3 (show CD3 Antibodies)-coupled signal transduction pathways.
Study investigated structures and thermodynamics of the interactions mediated by N-terminal Src homology 3 domain of CrkII and proline-rich motifs (PRMs) of cAbl kinase, highlight the role of interfacial water molecules and the conformational entropy in the SH3:PRM interactions
CrkII mediates IGF-1 (show IGF1 Antibodies) signaling and further balances pancreatic ductal adenocarcinoma biological behaviors via Erk1/2 and Akt (show AKT1 Antibodies) pathway
In individuals with class I 17p13.3 microduplications including CRK, we recommend biochemical evaluation of the growth hormone axis. Providers caring for these patients should be aware of their possible risk for the development of central precocious puberty.
Crk Tyr251 phosphorylation regulate invasive cell phenotypes in glioblastoma.
CsA (show ERCC8 Antibodies) and FK506 might interfere with selected effector T cell functions via a CrkII-, but not CrkI-dependent mechanisms.
Studied the role of PAK1/Crk axis in transduction of the oncogenic KRAS signal in non-small cell lung cancer (NSCLC).
These results indicate that CCRK (show CDK20 Antibodies) functions in eye development by both positively and negatively regulating the Hh pathway, and they reveal distinct requirements for Hh signaling in patterning and morphogenesis of the eyes.
the data suggest that CCRK (show CDK20 Antibodies) positively regulates the kinetics by which ciliary proteins such as Smoothened and Gli2 (show GLI2 Antibodies) are imported into the cilium, and that the efficiency of ciliary recruitment allows for potent responses to Hedgehog (show SHH Antibodies) signaling over long time periods.
results suggest that Crk and CrkL (show CRKL Antibodies) play essential overlapping roles in fibroblast growth.
both Crk and CrkL are required for the acquisition of cellular transformation by v-fos, whereas Crk plays a more prominent role than CrkL in v-ras-induced transformation.
results support a model in which Dok1 (show DOK1 Antibodies) phosphorylation normally suppresses localized Ras pathway activity in Crk-transformed cells via recruitment and/or activation of RasGAP (show RASA1 Antibodies)
Differential migration of CRK/CRKL (show CRKL Antibodies)-deficient T cells resulted in efficient graft-versus-leukemia responses with minimal graft-versus-host disease in mice.
Crk1 (show MAPK14 Antibodies)/2 and CrkL (show CRKL Antibodies) are physically linked, functionally complement each other during podocyte foot process spreading, and together are required for developing typical foot process architecture.
Data suggest that interactions between Crk (proto-oncogene (show RAB1A Antibodies) proteins c-crk) and Sos1 (Son of Sevenless homolog 1 (show SOS1 Antibodies)) involve electrostatic interactions at binding sites.
Results suggest that Crk and CrkL (show CRKL Antibodies) have critical roles in cell structure and motility by maintaining cytoskeletal integrity.
The v-Crk-myosin-1c interaction, which modulates membrane dynamics by regulating Rac1 activity, is crucial for cell adhesion and spreading.
This gene encodes a member of an adapter protein family that binds to several tyrosine-phosphorylated proteins. The product of this gene has several SH2 and SH3 domains (src-homology domains) and is involved in several signaling pathways, recruiting cytoplasmic proteins in the vicinity of tyrosine kinase through SH2-phosphotyrosine interaction. The N-terminal SH2 domain of this protein functions as a positive regulator of transformation whereas the C-terminal SH3 domain functions as a negative regulator of transformation. Two alternative transcripts encoding different isoforms with distinct biological activity have been described.
, adapter molecule crk
, v-crk sarcoma virus CT10 oncogene homolog (avian)
, proto-oncogene c-Crk
, avian sarcoma virus CT10 (v-crk) oncogene homolog
, proto-oncogene C-crk
, v-crk sarcoma virus CT10 oncogene homolog
, SH2/SH3 adaptor Crk2
, SH2/SH3 adaptor crk
, CT-10 related kinase 3
, proto-oncogene c-crk
, v-crk sarcoma virus CT10 oncogene-like protein