Use your antibodies-online credentials, if available.
Il n’y a pas de produits dans votre liste de comparaison.
Votre panier est vide.
The protein encoded by LIMS1 is an adaptor protein which contains five LIM domains, or double zinc fingers. De plus, nous expédions LIM and Senescent Cell Antigen-Like Domains 1 Protéines (5) et LIM and Senescent Cell Antigen-Like Domains 1 Kits (1) et beaucoup plus de produits pour cette protéine.
Showing 10 out of 50 products:
Chicken Monoclonal LIMS1 Primary Antibody pour IF, WB - ABIN968920
Campana, Myers, Rearden: Identification of PINCH in Schwann cells and DRG neurons: shuttling and signaling after nerve injury. dans Glia 2003
Show all 3 references for ABIN968920
Human Monoclonal LIMS1 Primary Antibody pour FACS, IF - ABIN966832
Yang, Wang, Hawkins, Chen, Vaynberg, Mao, Tu, Zuo, Wang, Wang, Wu, Tjandra, Qin: Structural basis of focal adhesion localization of LIM-only adaptor PINCH by integrin-linked kinase. dans The Journal of biological chemistry 2009
Show all 2 references for ABIN966832
Human Monoclonal LIMS1 Primary Antibody pour EIA, IF - ABIN1108043
Chiswell, Zhang, Murphy, Boggon, Calderwood: The structural basis of integrin-linked kinase-PINCH interactions. dans Proceedings of the National Academy of Sciences of the United States of America 2008
Show all 2 references for ABIN1108043
Mammalian cells have two functional PINCH proteins, PINCH1 and PINCH2 (Montrer LIMS2 Anticorps). PINCH not only binds to Nck2 (Montrer NCK2 Anticorps) and engages in the signaling of growth factor receptors, but also forms a ternary complex with ILK (Montrer ILK Anticorps) and parvin (Montrer PARVA Anticorps) (IPP (Montrer IPP Anticorps) complex).
our data suggest an essential role of PINCH1, ILK (Montrer ILK Anticorps) and ILKAP (Montrer ILKAP Anticorps) for the radioresistance of p53 (Montrer TP53 Anticorps)-wildtype glioblastoma multiforme cells
Data suggest that PINCH1 and Nck2 (Montrer NCK2 Anticorps) critically participate in the regulation of cellular radiosensitivity and EGFR (Montrer EGFR Anticorps) function and downstream signaling in a cellular model of human squamous cell carcinoma.
Downregulation of PINCH1 is associated with metastatic breast cancer.
changes in CSF (Montrer CSF2 Anticorps) levels of PINCH appear to correlate with changes in blood CD4 (Montrer CD4 Anticorps) count and with changes in CSF (Montrer CSF2 Anticorps) hyperphosphorylated Tau levels
two novel genes, galectin 9 (Montrer LGALS9 Anticorps) and PINCH, were expressed at much higher levels in cancerous lesions than in normal tissues in all the patients with clear-cell carcinoma who were examined
PINCH predicts survival in rectal cancer patients with RT, but not in patients without RT. The expression of PINCH may be regulated by radiation and by environmental factors surrounding the cells.
PINCH is increased and binds to hp-Tau. These studies address a new mechanism by which AD and HIV may intersect and identify PINCH as a contributing factor to the accumulation of hyperphosphorylated Tau.
Pinch-1 mRNA and protein were significantly up-regulated in acute lymphoblastic leukemia and acute myeloid leukemia (Montrer BCL11A Anticorps) bone marrow stromal cells compared to normal bone marrow stromal cells (p<0.01).
PINCH protein might play an important role in the tumourigenesis and metastasis of gastric adenocarcinoma.
findings suggest that PINCH-1 regulates integrin-mediated adhesion of keratinocytes through the interactions with ILK (Montrer ILK Anticorps) as well as EPLIN (Montrer LIMA1 Anticorps).
Rsu-1 (Montrer RSU1 Anticorps) expression is dramatically decreased in PINCH double knockout mouse livers.
PINCH-1 inhibits JNK (Montrer MAPK8 Anticorps)-mediated apoptosis by stabilising the PINCH-1 binding protein RSU-1 (Montrer RSU1 Anticorps) and promotes Bcl-2 (Montrer BCL2 Anticorps)-dependent pro-survival signalling downstream of integrins.
Data suggest that the adapter protein (Montrer GRB10 Anticorps) PINCH1 critically participates in the regulation of the cellular radiosensitivity of normal and malignant cells similarly under adhesion and suspension conditions.
PINCH1 plays an essential role in early murine embryonic development but is dispensable in ventricular cardiomyocytes.
These results provide important evidence for a crucial role of the PINCH-1-ILK (Montrer ILK Anticorps)-alpha-parvin (Montrer PARVA Anticorps) complex in the control of podocyte adhesion, morphology, and survival.
LIM (Montrer PDLIM5 Anticorps) 5 domain of PINCH1 interacts with Rsu-1 (Montrer RSU1 Anticorps) in mammalian cells and functions, in part, by altering cell adhesion.
The PINCH1 is composed of 5 LIM domains, binds ILK and locates to integrin-mediated adhesion sites, and PINCH1 is for integrin function, actin organization, cell-cell adhesion and endodermal cell survival during the implanting of mouse embryos.
PICH1, Ilk (Montrer ILK Anticorps) and alpha-parvin (Montrer PARVA Anticorps) form a complex to costameres in neonatal mouse ventricular myocytes. This complex is stimulated by fibronectins and phenylephrine, and by both by drug synergism, to regulate cardiac myocyte hypertrophy.
The protein encoded by this gene is an adaptor protein which contains five LIM domains, or double zinc fingers. The protein is likely involved in integrin signaling through its LIM domain-mediated interaction with integrin-linked kinase, found in focal adhesion plaques. It is also thought to act as a bridge linking integrin-linked kinase to NCK adaptor protein 2, which is involved in growth factor receptor kinase signaling pathways. Its localization to the periphery of spreading cells also suggests that this protein may play a role in integrin-mediated cell adhesion or spreading. Several transcript variants encoding different isoforms have been found for this gene.
LIM and senescent cell antigen-like-containing domain protein 1
, particularly interesting new Cys-His protein 1
, renal carcinoma antigen NY-REN-48