Nuclear Pore-O-Linked Glycoprotein Antibodies
We offer Nuclear Pore-O-Linked Glycoprotein Antibodies for use in common research applications: Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Immunohistochemistry-Paraffin, Immunoprecipitation, Western Blot. Each Nuclear Pore-O-Linked Glycoprotein Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our Nuclear Pore-O-Linked Glycoprotein Antibodies can be used in a variety of model species: Human, Mammal, Mouse, Rat, Xenopus, Yeast. Use the list below to choose the Nuclear Pore-O-Linked Glycoprotein Antibody which is most appropriate for your research; you can click on each one to view full technical details, images, references, reviews and related products. Choose from our Nuclear Pore-O-Linked Glycoprotein monoclonal antibodies.
Alternate Names for Nuclear Pore-O-Linked Glycoprotein Antibodies
anti-Nuclear Pore-O-Linked Glycoprotein antibody
1 Results for "nuclear-pore-o-linked-glycoprotein" in Primary Antibodies
![Immunohistochemistry-Paraffin: Nuclear Pore-O-Linked Glycoprotein Antibody (RL1) [NB600-1068] - Immunohistochemistry was performed on normal biopsies of deparaffinized Rat lymph node tissue. To expose target proteins, heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1:200 with a mouse monoclonal antibody recognizing Nuclear Pore-O-Linked Glycoprotein or without primary antibody (negative control) overnight at 4C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Tissues were counterstained with hematoxylin and prepped for mounting.](http://images.novusbio.com/fullsize/Nuclear-Pore-O-Linked-Glycoprotein-Antibody-RL1-Immunohistochemistry-Paraffin-NB600-1068-img0003.jpg "Immunohistochemistry-Paraffin: Nuclear Pore-O-Linked Glycoprotein Antibody (RL1) [NB600-1068] - Immunohistochemistry was performed on normal biopsies of deparaffinized Rat lymph node tissue. To expose target proteins, heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1:200 with a mouse monoclonal antibody recognizing Nuclear Pore-O-Linked Glycoprotein or without primary antibody (negative control) overnight at 4C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Tissues were counterstained with hematoxylin and prepped for mounting.")
![Immunohistochemistry-Paraffin: Nuclear Pore-O-Linked Glycoprotein Antibody (RL1) [NB600-1068] - Immunohistochemistry was performed on normal biopsies of deparaffinized Rat brain tissue. To expose target proteins, heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1:200 with a mouse monoclonal antibody recognizing Nuclear Pore-O-Linked Glycoprotein or without primary antibody (negative control) overnight at 4C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Tissues were counterstained with hematoxylin and prepped for mounting.](http://images.novusbio.com/fullsize/Nuclear-Pore-O-Linked-Glycoprotein-Antibody-RL1-Immunohistochemistry-Paraffin-NB600-1068-img0001.jpg)
![Immunohistochemistry-Paraffin: Nuclear Pore-O-Linked Glycoprotein Antibody (RL1) [NB600-1068] - Immunohistochemistry was performed on normal biopsies of deparaffinized Rat kidney tissue. To expose target proteins, heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1:200 with a mouse monoclonal antibody recognizing Nuclear Pore-O-Linked Glycoprotein or without primary antibody (negative control) overnight at 4C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Tissues were counterstained with hematoxylin and prepped for mounting.](http://images.novusbio.com/fullsize/Nuclear-Pore-O-Linked-Glycoprotein-Antibody-RL1-Immunohistochemistry-Paraffin-NB600-1068-img0002.jpg)