catalog number :
MBS718282
products type :
Recombinant Protein
products full name :
Recombinant Mouse Lysyl oxidase homolog 2
products short name :
Lysyl oxidase homolog 2
products name syn :
Lysyl oxidase-like protein 2
other names :
lysyl oxidase homolog 2; Lysyl oxidase homolog 2; lysyl oxidase homolog 2; lysyl oxidase-like 2; Lysyl oxidase-like protein 2
products gene name :
Loxl2
other gene names :
Loxl2; Loxl2; 1110004B06Rik; 4930526G11Rik; 9430067E15Rik
uniprot entry name :
LOXL2_MOUSE
host :
E Coli or Yeast or Baculovirus or Mammalian Cell
sequence positions :
26-776
sequence :
QYEGWPYQLQYPEYFQQPAPEHHQRQVPSDVVKIQVRLA
GQKRKHNEGRVEVYYEGQWGTVCDDDFSIHAAHVVCRQV
GYVEAKSWAASSSYGPGEGPIWLDNIYCTGKESTLASCS
SNGWGVTDCKHTEDVGVVCSEKRIPGFKFDNSLINQIES
LNIQVEDIRIRPILSAFRHRKPVTEGYVEVKEGKAWKQI
CNKHWTAKNSHVVCGMFGFPAEKTYNPKAYKTFASRRKL
RYWKFSMNCTGTEAHISSCKL
purity :
Greater than 90% as determined by SDS-PAGE.
form :
Liquid containing glycerol; lyophilization may be available upon request.
storage stability :
Store at -20 degree C, for extended storage, conserve at -20 degree C or -80 degree C.
products description :
Mediates the post-translational oxidative deamination of lysine residues on target proteins leading to the formation of deaminated lysine (allysine). When secreted in extracellular matrix, promotes cross-linking of extracellular matrix proteins by mediating oxidative deamination of peptidyl lysine residues in precursors to fibrous collagen and elastin. Acts as a regulator of sprouting angiogenesis, probably via collagen IV scaffolding. When nuclear, acts as a transcription corepressor and specifically mediates deamination of trimethylated 'Lys-4' of histone H3 (H3K4me3), a specific tag for epigenetic transcriptional activation. Involved in epithelial to mesenchymal transition (T) via interaction with SNAI1 and participates in repression of E-cadherin, probably by mediating deamination of histone H3. Acts as a regulator of chondrocyte differentiation, probably by regulating expression of factors that control chondrocyte differentiation. 1 Publication
ncbi acc num :
NP_201582.2
ncbi gb acc num :
NM_033325.2
ncbi mol weight :
88.48kD
uniprot summary :
LOXL2: Mediates the post-translational oxidative deamination of lysine residues on target proteins leading to the formation of deaminated lysine (allysine). When secreted in extracellular matrix, promotes cross-linking of extracellular matrix proteins by mediating oxidative deamination of peptidyl lysine residues in precursors to fibrous collagen and elastin. Acts as a regulator of sprouting angiogenesis, probably via collagen IV scaffolding. When nuclear, acts as a transcription corepressor and specifically mediates deamination of trimethylated 'Lys-4' of histone H3 (H3K4me3), a specific tag for epigenetic transcriptional activation. Involved in epithelial to mesenchymal transition (EMT) via interaction with SNAI1 and participates in repression of E- cadherin, probably by mediating deamination of histone H3. Also involved in E-cadherin repression following hypoxia, a hallmark of epithelial to mesenchymal transition believed to amplify tumor aggressiveness, suggesting that it may play a role in tumor progression. Acts as a regulator of chondrocyte differentiation, probably by regulating expression of factors that control chondrocyte differentiation. Belongs to the lysyl oxidase family. Protein type: Secreted; Cell adhesion; Oxidoreductase; EC 1.4.3.13; Secreted, signal peptide. Cellular Component: basement membrane; chromosome; extracellular region; extracellular space; membrane; nucleoplasm; nucleus; proteinaceous extracellular matrix. Molecular Function: chromatin binding; copper ion binding; metal ion binding; methylated histone residue binding; oxidoreductase activity; oxidoreductase activity, acting on the CH-NH2 group of donors, oxygen as acceptor; protein-lysine 6-oxidase activity; scavenger receptor activity; transcription corepressor activity. Biological Process: chromatin modification; collagen fibril organization; endothelial cell migration; endothelial cell proliferation; epithelial to mesenchymal transition; histone modification; negative regulation of transcription, DNA-dependent; positive regulation of chondrocyte differentiation; protein amino acid deamination; protein modification process; regulation of transcription, DNA-dependent; response to copper ion; response to hypoxia; sprouting angiogenesis; transcription, DNA-dependent