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Human Polyclonal LOXL2 Primary Antibody für ICC, IF - ABIN442901
Wong, Zhang, Gilkes, Chen, Wei, Chaturvedi, Hubbi, Semenza: Inhibitors of hypoxia-inducible factor 1 block breast cancer metastatic niche formation and lung metastasis. in Journal of molecular medicine (Berlin, Germany) 2012
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Human Monoclonal LOXL2 Primary Antibody für ELISA, WB - ABIN561690
Fujimoto, Tajima: Reciprocal regulation of LOX and LOXL2 expression during cell adhesion and terminal differentiation in epidermal keratinocytes. in Journal of dermatological science 2009
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Human Monoclonal LOXL2 Primary Antibody für WB - ABIN2724865
Park, Lee, Lee, Kim, Dong, Yoon: Emerging role of LOXL2 in the promotion of pancreas cancer metastasis. in Oncotarget 2018
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Human Monoclonal LOXL2 Primary Antibody für IHC - ABIN2724866
Park, Jo, Kim, Kim, Lee, Park, Kim, Lee, Kim, Park, Dong, Lee: Role of LOXL2 in the epithelial-mesenchymal transition and colorectal cancer metastasis. in Oncotarget 2017
Human Polyclonal LOXL2 Primary Antibody für ELISA, WB - ABIN561689
Ghiggeri, Gigante, Di Donato et al.: Constitutional Nephrin Deficiency in Conditionally Immortalized Human Podocytes Induced Epithelial-Mesenchymal Transition, Supported by β-Catenin/NF-kappa B Activation: A Consequence of Cell Junction ... in International journal of nephrology 2014
stimulates gingival fibroblast proliferation, likely by a platelet-derived growth factor B receptor-mediated mechanism
LOX and LOXL2 played important roles in trophoblast cell migration and invasion by altering the TGF-beta1/Smad3 pathway to modulate collagen expression.
Results demonstrated that the expression of LOXL2 in renal cell carcinoma (RCC) tissues was increased compared with that in adjacent normal tissues. Its silencing inhibits the EMT, proliferation and invasion of RCC cells through the Src/FAK signaling pathway.
Upon secretion in cell culture, LOXL2 undergoes proteolytic processing of the first two of four scavenger receptor cysteine-rich domains at the N-terminus. Processing occurred at (314)Arg-(315)Phe-(316)Arg-(317)Lys downward arrow-(318)Ala-, implicating proprotein convertases.
LOXL2 plays an important role in the development of cellular radioresistance in castration-resistant prostate cancer (CRPC) cells. Targeting LOXL2 may be a rational avenue to overcome radioresistance in CRPC cells. A LOXL2-targeting strategy for CRPC treatment warrants detailed investigation in the future.
Compressive moduli of LOXL2-treated constructs are similar to untreated constructs.
our study elucidates a novel function of tumor cell secreted LOXL2 in lymphangiogenesis and lymph node metastasis, demonstrating that LOXL2 serves as a promising target for anti-lymphangiogenesis and anti-metastasis therapies for breast cancer.
Our present data suggest that decreased elastin renewal due to LOXL2 mutations and consecutive reduced LOXL2 expression contribute to the pathogenesis of MDE.
although Loxl2 is expressed in both dermis and epidermis, its function appears largely confined to the epidermis.
we report that overexpression of LOXL2 promotes its accumulation in the Endoplasmic Reticulum where it interacts with HSPA5 leading to activation of the IRE1-XBP1 signalling pathway of the ER-stress response.
Copper loading robustly activates hLOXL2 and supports lysyl tyrosylquinone formation.
LOXL2 might have an important role in CRC.
Results revealed that LOXL2 expression was higher in hepatocellular carcinoma (HCC) cell lines and tissues. There was a significant correlation between EMT status and LOXL2 levels indicated that a higher level of LOXL2 may contribute to tumor progression.
Plasma LOXL2 was significantly elevated and also strongly correlated with the degree of left atrial fibrosis in Atrial fibrillation patients with normal left ventricular function.
LOXL2 may be involved in the pathogenesis of rheumatoid arthritis-associated interstitial lung disease and might be helpful in early diagnosis of RA-ILD.
LOXL1/LOXL2 gene expression and protein levels were increased in Idiopathic pulmonary fibrosis (IPF) versus non-IPF.
This study focused on the relationship between lysyl oxidase (LOX), LOX-like protein 1 (LOXL1), and LOXL2 and pulmonary emphysema pathogenesis.
Glomerular LOXL2 was localized to the cytoplasm of podocytes, as determined by double immunofluorescence microscopy using a podocyte marker (synaptopodin). This result was supported by western blot analysis, which demonstrated that LOXL2 protein expression is present in cultured human podocytes and HK2 human proximal tubular cells.
Lysyl oxidase like-2 (LOXL2) overexpression differentially regulates signaling pathways in osteoarthritis chondrocytes.
our data reveal that the tumor-promoting role of LOXL2 in ESCC is mediated by perturbing the architecture of actin cytoskeleton through its PPIs.
Dmloxl-1 and Dmloxl-2 are differentially expressed; active DmLOXL-1 influences gene expression and development
Study shows that the levels of Loxl2 mRNA and protein are elevated in renal cortex and glomeruli of COL4A3-KO Alport mice, a model for chronic kidney disease.
The present data provides a comprehensive analysis of the LOXL2 in pulmonary fibrosis.
LOXL2 controls myofibroblast transformation and migration.
The mRNA and protein expression levels of LOXL2 were higher in a mouse model of tubulointerstitial fibrosis compared with in control mice.
Findings indicate a pathophysiologic role and function for lysyl oxidase-like protein LOXL2 in breast cancer metastasis.
Insulin resistance promotes lysyl oxidase like 2 induction and fibrosis accumulation in non-alcoholic fatty liver disease.
glomerular extracellular matrix. Altogether, we demonstrate that LOXL2 is a novel component of the molecular machinery that forms cross-linked collagen IV networks, which are essential for glomerular basement membrane stability and molecular ultrafiltration function.
LOX and LOXL2 may play an important role in the pathogenesis of AMD. Targeting LOXL2 could have a broader efficacy than targeting LOX, by reducing angiogenesis and inflammation, as well as fibrosis.
Loss and gain of function analyses combined with in vivo studies in syngeneic breast cancer models demonstrate the participation of LOXL2 and E47 in tumor growth and their requirement for lung metastasis.
promoted intrahepatic metastasis by increasing tissue stiffness
Findings reveal new insight into the mechanisms of fibroblast activation, a novel function of LOXL2, and further highlight the importance of generating LOXL2-targeted therapies for the prevention of tumor progression and metastasis.
The Snail1 transcription factor represses mouse pericentromeric transcription, acting through the H3K4 deaminase LOXL2.
The enzymatic activity of lysyl oxidas-like-2 (LOXL2) is not required for LOXL2-induced inhibition of keratinocyte differentiation.
This study provides the first evidence for the role of LOXL2 in regulating angiogenesis through collagen IV scaffolding.
LOXL2 promotes chondrocyte differentiation by mechanisms that are likely to include roles as both a regulator and an effector of chondrocyte differentiation
The efficacy and safety of LOXL2-specific monoclonal antibody represents a new therapeutic approach with broad applicability in oncologic and fibrotic diseases.
LoxL2 is not expressed in MC3T3-E1 cells.
results suggest that LOXL2 could be an appealing target for treatment of scar formation after glaucoma surgery, and point to the potential therapeutic benefits of simtuzumab, a humanized monoclonal antibody derived from GS-607601.
This gene encodes a member of the lysyl oxidase gene family. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyses the first step in the formation of crosslinks in collagens and elastin. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family.
lysyl oxidase homolog 2
, lysyl oxidase related 2
, lysyl oxidase-like protein 2
, lysyl oxidase-related protein 2
, lysyl oxidase-related protein WS9-14
, lysyl oxidase-like 2
, Lysyl oxidase-like protein 2
, lysyl oxidase homolog 2-like
, Lysyl oxidase homolog 2
, Lysyl oxidase-like protein 2B