Human LOXL2 Protein, Fc Tag

Proteins and Peptides

貨號 Cat. No.
LO2-H525x
規格 Size
50ug
品牌 Brand
ACROBiosystems
Species
Human
Conjugate
Unconjugated
Expression System
HEK293
Tag
Fc Tag

Description




Source : 


Human LOXL2, Fc Tag (LO2-H525x) is expressed from human 293 cells (HEK293). It contains AA Gln 26 - Gln 774 (Accession # NP_002309).


 

Molecule : LOXL2


 

Synonyms : Lysyl oxidase homolog 2,LOXL2


 

Format : Powder


 

Category : Enzymes


 

Accession : NP_002309


 

Storage : -20℃


 

Shipping condition : Powder,RT


 

Molecular Weight : 111.6 kDa


 

Characteristics :


This protein carries a human IgG1 Fc tag at the C-terminus. The protein has a calculated MW of 111.6 kDa. As a result of Glycosylation, the protein migrates as 120-130 kDa under reducing (R) condition, and 200-240 kDa under non-reducing (NR) condition (SD


 

Endotoxin Level : Less than 1.0 EU per μg by the LAL method.


 

Buffer : Tris with Glycine, Arginine and NaCl, pH7.5


 

Description :


Lysyl oxidase homolog 2 is also known as LOXL2, Lysyl oxidase-like protein 2, which is expressed in many tissues, highest expression in reproductive tissues, placenta, uterus and prostate, Up-regulated in a number of cancers cells and tissues. 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. LOXL2 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. LOXL2 acts as a regulator of chondrocyte differentiation, probably by regulating expression of factors that control chondrocyte differentiation.


 

References :


(1) Ota T.,we al.,2004, Nat. Genet. 36:40-45.
(2) Jourdan-Le Saux C.,et al., 1999, J. Biol. Chem. 274:12939-12944.
(3) Lugassy J.,et al., 2012, J. Biol. Chem. 287:3541-3549.





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