catalog number :
MBS9200546
products full name :
LOX Antibody (Center) (Ascites)
products short name :
[LOX]
products name syn :
[Protein-lysine 6-oxidase; Lysyl oxidase; LOX]
other names :
[protein-lysine 6-oxidase isoform 1 preproprotein; Protein-lysine 6-oxidase; protein-lysine 6-oxidase; lysyl oxidase; Lysyl oxidase]
products gene name :
[LOX]
other gene names :
[LOX; LOX]
uniprot entry name :
LYOX_HUMAN
reactivity :
Human (Predicted Reactivity: Mouse, Pig, Rat)
sequence positions :
[234-260]
specificity :
This LOX antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 234-260 amino acids from the Central region of human LOX.
form :
Mouse monoclonal antibody supplied in crude ascites with 0.09% (W/V) sodium azide.
storage stability :
Maintain refrigerated at 2-8 degree C for up to 2 weeks. For long term storage store at -20 degree C in small aliquots to prevent freeze-thaw cycles.
tested application :
Western Blot (WB), ELISA (EIA)
app notes :
WB~~1:200~1600
image1 heading :
Western Blot (WB)
other info1 :
Antigen Type: Synthetic Peptide
other info2 :
Antigen Source: HUMAN. Function: Responsible for the post-translational oxidative deamination of peptidyl lysine residues in precursors to fibrous collagen and elastin. In addition to cross-linking of extracellular matrix proteins, may have adirect role in tumor suppression. Cellular Location: Secreted, extracellular space. Tissue Location: Heart, placenta, skeletal muscle, kidney, lung and pancreas.
products categories :
Cancer; Cardiovascular; Signal Transduction
products description :
The protein encoded by this gene is an extracellular. copper enzyme that initiates the crosslinking of collagens and. elastin. The enzyme catalyzes oxidative deamination of the. epsilon-amino group in certain lysine and hydroxylysine residues of. collagens and lysine residues of elastin. In addition to. crosslinking extracellular matrix proteins, the encoded protein may. have a role in tumor suppression. Defects in this gene are a cause. of autosomal recessive cutis laxa type I (CL type I). Two. transcript variants encoding different isoforms have been found for. this gene.
products references :
Gao, Y., et al. Proc. Natl. Acad. Sci. U.S.A. 107(44):18892-18897(2010). Santhanam, A.N., et al. Oncogene 29(27):3921-3932(2010). Liu, C.Y., et al. Carcinogenesis 31(7):1259-1263(2010). Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) :. Wang, X., et al. PLoS ONE 5 (8), E11934 (2010) :
ncbi acc num :
NP_002308.2
ncbi gb acc num :
NM_002317.5
ncbi summary :
The protein encoded by this gene is an extracellular copper enzyme that initiates the crosslinking of collagens and elastin. The enzyme catalyzes oxidative deamination of the epsilon-amino group in certain lysine and hydroxylysine residues of collagens and lysine residues of elastin. In addition to crosslinking extracellular matrix proteins, the encoded protein may have a role in tumor suppression. Defects in this gene are a cause of autosomal recessive cutis laxa type I (CL type I). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]
uniprot summary :
LOX: Responsible for the post-translational oxidative deamination of peptidyl lysine residues in precursors to fibrous collagen and elastin. In addition to cross-linking of extracellular matrix proteins, may have a direct role in tumor suppression. Belongs to the lysyl oxidase family. Protein type: Secreted; Secreted, signal peptide; Oxidoreductase; EC 1.4.3.13. Chromosomal Location of Human Ortholog: 5q23.2. Cellular Component: proteinaceous extracellular matrix; extracellular space; collagen; extracellular region; nucleus. Molecular Function: protein binding; copper ion binding; protein-lysine 6-oxidase activity. Biological Process: response to drug; elastic fiber assembly; blood vessel development; extracellular matrix organization and biogenesis; collagen fibril organization; wound healing; response to steroid hormone stimulus; protein modification process; lung development. Disease: Cutis Laxa, Autosomal Recessive, Type Ia