Nuclear Pore-O-Linked Glycoprotein Antibody (RL1) - BSA Free
Novus Biologicals, part of Bio-Techne | Catalog # NB600-1068
Discontinued Product
NB600-1068 has been discontinued.
View all Nuclear Pore-O-Linked Glycoprotein products.
Key Product Details
Species Reactivity
Validated:
Human, Mouse, Rat, Mammal, Xenopus, Yeast
Cited:
Human
Applications
Immunohistochemistry, Immunohistochemistry-Paraffin, Western Blot, Immunofluorescence, Immunoprecipitation
Label
Unconjugated
Antibody Source
Monoclonal Mouse IgM Clone # RL1
Format
BSA Free
Concentration
Concentrations vary lot to lot. See vial label for concentration. If unlisted please contact technical services.
Product Specifications
Immunogen
Pore complex-lamina fraction purified from rat liver nuclear envelopes.
Reactivity Notes
Cross-reactivity with S. cerevisiae, Xenopus laevis and a wide variety of Mammals. Please note that this antibody is reactive to Mouse and derived from the same host, Mouse. Additional Mouse on Mouse blocking steps may be required for IHC and ICC experiments. Please contact Technical Support for more information.
Localization
Nuclear membrane
Specificity
Detects nuclear pore-O-linked glycoprotein
Clonality
Monoclonal
Host
Mouse
Isotype
IgM
Scientific Data Images for Nuclear Pore-O-Linked Glycoprotein Antibody (RL1) - BSA Free
Immunohistochemistry-Paraffin: Nuclear Pore-O-Linked Glycoprotein Antibody (RL1) [NB600-1068]
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-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.Immunohistochemistry-Paraffin: Nuclear Pore-O-Linked Glycoprotein Antibody (RL1) [NB600-1068]
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.Applications for Nuclear Pore-O-Linked Glycoprotein Antibody (RL1) - BSA Free
Application
Recommended Usage
Immunofluorescence
1:100
Immunohistochemistry
1:200
Immunohistochemistry-Paraffin
1:10 - 1:500
Immunoprecipitation
1:10 - 1:500
Western Blot
1:1000
Application Notes
WB: Detects up to eight different proteins from the nuclear pore complex (NPC) of approx. 210, 180, 145, 100, 63, 58, 54 and 45 kDa. IF: Staining of NPC O-linked glycoproteins with this antibody results in exclusive labeling of the NPC proteins on a wide variety of mammalian cells as well as S. cerevisiae and Xenopus. Labeling occurs exclusively at the NPC with most of the labeling at the cytoplasmic and nucleoplasmic margins.This antibody, if microinjected inhibits both protein import and RNA export in Xenopus oocytes.
Formulation, Preparation, and Storage
Purification
PEG purified
Formulation
PBS
Format
BSA Free
Preservative
0.05% Sodium Azide
Concentration
Concentrations vary lot to lot. See vial label for concentration. If unlisted please contact technical services.
Shipping
The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage
Store at -20C. Avoid freeze-thaw cycles.
Background: Nuclear Pore-O-Linked Glycoprotein
Product Documents for Nuclear Pore-O-Linked Glycoprotein Antibody (RL1) - BSA Free
Product Specific Notices for Nuclear Pore-O-Linked Glycoprotein Antibody (RL1) - BSA Free
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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