Rabbit Polyclonal LOX antibody. Suitable for WB and reacts with Mouse, Human samples. Cited in 77 publications.
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 98.98% PBS, 1% BSA
WB | |
---|---|
Human | Tested |
Mouse | Tested |
Rat | Predicted |
Chicken | Predicted |
Dog | Predicted |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1-5 µg/mL | Notes Abcam recommends using Milk as the blocking agent. |
Species Human | Dilution info 1-5 µg/mL | Notes Abcam recommends using Milk as the blocking agent. |
Species | Dilution info | Notes |
---|---|---|
Species Rat, Chicken, Dog | Dilution info - | Notes - |
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Responsible for the post-translational oxidative deamination of peptidyl lysine residues in precursors to fibrous collagen and elastin (PubMed:26838787). Regulator of Ras expression. May play a role in tumor suppression. Plays a role in the aortic wall architecture (By similarity).
Protein-lysine 6-oxidase, Lysyl oxidase, LOX
Rabbit Polyclonal LOX antibody. Suitable for WB and reacts with Mouse, Human samples. Cited in 77 publications.
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 98.98% PBS, 1% BSA
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False colour image of Western blot: Anti-LOX antibody staining at 1 ug/ml, shown in green; Mouse anti-GAPDH antibody [6C5] (Anti-GAPDH antibody [6C5] - Loading Control ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab31238 was shown to bind specifically to LOX. A band was observed at 50 kDa in wild-type HeLa cell lysates with no signal observed at this size in Lox knockout cell line Human LOX knockout HeLa cell line ab261801 (knockout cell lysate ab256981). To generate this image, wild-type and Lox knockout HeLa cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3 % milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed ab216776) at 1/20000 dilution.
All lanes: Western blot - Anti-LOX antibody (ab31238) at 1 µg/mL
Lane 1: Wild-type HeLa cell lysate at 20 µg
Lane 2: Wild-type HeLa Treated DFO (0.5 mM, 24 h) cell lysate at 20 µg
Lane 2: Western blot - Human LOX knockout HeLa cell line (Human LOX knockout HeLa cell line ab261801)
Lane 3: LOX knockout HeLa Vehicle Control DFO (0 mM, 24 h) cell lysate at 20 µg
Lane 4: LOX knockout HeLa Treated DFO (0.5 mM, 24 h) cell lysate at 20 µg
Performed under reducing conditions.
Predicted band size: 47 kDa
Observed band size: 50 kDa
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 2% Bovine Serum Albumin before being incubated with ab31238 overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP, and visualised using ECL development solution ECL Substrate Kit (High Sensitivity) ab133406.
All lanes: Western blot - Anti-LOX antibody (ab31238) at 1 µg/mL
Lane 1: MDA-MB-361 (Human breast adenocarcinoma cell line) Whole Cell Lysate at 10 µg
Lane 2: MEF1 (Mouse embryonic fibroblast cell line) Whole Cell Lysate at 10 µg
Lane 3: NIH 3T3 (Mouse) Whole Cell Lysate at 10 µg
All lanes: Goat Anti-Rabbit IgG H&L (HRP) preadsorbed at 1/50000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 47 kDa
Observed band size: 15 kDa, 36 kDa, 47 kDa, 52 kDa
Exposure time: 4min
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