Western Blot<br />
Positive WB detected in: MCF-7 whole cell lysate, PC3 whole cell lysate, Mouse brain tissue, Rat brain tissue<br />
All lanes: LOXL2 antibody at 1:2000<br />
Secondary<br />
Goat polyclonal to rabbit IgG at 1/50000 dilution<br />
Predicted band size: 87 kDa<br />
Observed band size: 53 kDa<br />
Western Blot<br />
Positive WB detected in: MCF-7 whole cell lysate, PC3 whole cell lysate, Mouse brain tissue, Rat brain tissue<br />
All lanes: LOXL2 antibody at 1:2000<br />
Secondary<br />
Goat polyclonal to rabbit IgG at 1/50000 dilution<br />
Predicted band size: 87 kDa<br />
Observed band size: 53 kDa<br />IHC image of CSB-RA907007A0HU diluted at 1:100 and staining in paraffin-embedded human prostate tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4℃ overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.IHC image of CSB-RA907007A0HU diluted at 1:100 and staining in paraffin-embedded human placenta tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4℃ overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.Immunofluorescence staining of HepG2 Cells with CSB-RA907007A0HU at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% TritonX-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4℃. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L).

Anti LOXL2 mAb (Clone 2E5)

CusaBio

Catalog No:
CSB-RA907007A0HU-50
$221.00
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.

Product Specifications
Application WB, IHC, IF, FC, ELISA
Reactivity Human, Mouse, Rat
Clonality Monoclonal (Clone No.: 200000)
Documents & Links for Anti LOXL2 mAb (Clone 2E5)
Datasheet Anti LOXL2 mAb (Clone 2E5) Datasheet
Vendor Page Anti LOXL2 mAb (Clone 2E5) at CUSABIO

Documents & Links for Anti LOXL2 mAb (Clone 2E5)
Datasheet Anti LOXL2 mAb (Clone 2E5) Datasheet
Vendor Page Anti LOXL2 mAb (Clone 2E5)