Anti-Nuclear Pore Complex Proteins antibody [Mab414] ab24609 is a mouse monoclonal antibody that is used in Nuclear Pore Complex Proteins western blotting, IHC and immunofluorescence. Suitable for human, mouse and rat samples.
- Antibody clone Mab414 is the most widely used clone for Nuclear Pore Complex Proteins on the market
Preservative: 0.03% Thimerosal (merthiolate)
Constituents: PBS
ICC/IF | IHC-P | WB | |
---|---|---|---|
Human | Tested | Tested | Tested |
Mouse | Tested | Expected | Tested |
Rat | Expected | Expected | Tested |
Saccharomyces cerevisiae | Tested | Expected | Expected |
Vertebrata | Predicted | Predicted | Predicted |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes Fix cells with 4% paraformaldehyde in NWB (200 mM sucrose, 15 mM Hepes, pH 7.4, 50 mM NaCl, 2.5 mM MgCl2, and 1 mM DTT). Permeabilise with 0.1% NP-40 or 0.1% Triton X-100 in PBS for 2 min. (see Lopez-Soler reference); different customer have used this antibody at different dilutions for ICC/IF (see images below). We recommend that optimal working dilutions are determined by each customer. |
Species Saccharomyces cerevisiae | Dilution info - | Notes Fix cells with 4% paraformaldehyde in NWB (200 mM sucrose, 15 mM Hepes, pH 7.4, 50 mM NaCl, 2.5 mM MgCl2, and 1 mM DTT). Permeabilise with 0.1% NP-40 or 0.1% Triton X-100 in PBS for 2 min. (see Lopez-Soler reference); different customer have used this antibody at different dilutions for ICC/IF (see images below). We recommend that optimal working dilutions are determined by each customer. |
Species Human | Dilution info - | Notes Fix cells with 4% paraformaldehyde in NWB (200 mM sucrose, 15 mM Hepes, pH 7.4, 50 mM NaCl, 2.5 mM MgCl2, and 1 mM DTT). Permeabilise with 0.1% NP-40 or 0.1% Triton X-100 in PBS for 2 min. (see Lopez-Soler reference); different customer have used this antibody at different dilutions for ICC/IF (see images below). We recommend that optimal working dilutions are determined by each customer. |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Vertebrata | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 0.5-1 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Saccharomyces cerevisiae, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Vertebrata | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/2000 - 1/5000 | Notes - |
Species Mouse | Dilution info 1/2000 - 1/5000 | Notes - |
Species Rat | Dilution info 1/2000 - 1/5000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Saccharomyces cerevisiae | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Vertebrata | Dilution info - | Notes - |
Anti-Nuclear Pore Complex Proteins antibody [Mab414] ab24609 is a mouse monoclonal antibody that is used in Nuclear Pore Complex Proteins western blotting, IHC and immunofluorescence. Suitable for human, mouse and rat samples.
- Antibody clone Mab414 is the most widely used clone for Nuclear Pore Complex Proteins on the market
Preservative: 0.03% Thimerosal (merthiolate)
Constituents: PBS
This is a reliable general purpose monoclonal antibody which recognizes a related family of NPC proteins. This antibody is ideal for studying the morphology and composition of the nucleus and nuclear envelope. It is also useful in studying changes in the nuclear structure during mitosis and meiosis.
This product was changed from ascites to tissue culture supernatant on 20/05/2019. Please note that the dilutions may need to be adjusted accordingly. If you have any questions, please do not hesitate to contact our scientific support team.
The Nuclear Pore Complex Proteins often called pore proteins or NPC proteins are large structures that form channels in the nuclear envelope. These proteins have a mass of about 120 MDa. They are expressed in the nuclear envelope of eukaryotic cells. NPC proteins function as gates for molecules traveling in and out of the nucleus regulating the entry and exit of proteins RNA and other macromolecules. Alternative names like 'pore complex' and 'nucleus pores' are sometimes used to describe these structures.
NPC proteins enable the exchange of molecules between the nucleus and the cytoplasm. They are part of the NPC complex integrating several different proteins in a highly coordinated manner. These proteins manage transport through nuclear pore by selectively allowing the passage of certain molecules while blocking others. This selective permeability ensures that essential cellular processes such as DNA replication and transcription occur efficiently within the nucleus.
NPC proteins participate significantly in nucleocytoplasmic transport pathways and gene expression regulation pathways. They are involved with proteins like importins and exportins that mediate the transport of molecules across the nuclear envelope. Importin β for example facilitates the transport of proteins into the nucleus while exportin mediates the export of RNA and ribonuclear proteins.
Alterations in NPC proteins have links to specific conditions such as cancer and neurodegenerative diseases. Abnormalities in NPC function are associated with the mislocalization of proteins and RNA contributing to disease pathogenesis. One protein related to these disorders is TPR (Translocated Promoter Region) which can interact with NPC proteins and has roles in cell cycle regulation and chromatin organization.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
ab24609 staining Nuclear Pore Complex Proteins in Human chronic myelogenous leukemia cells from bone marrow cells. Cells were fixed with 4% paraformaldehyde in DPBS buffer for 20 mins and permeabilised with 0.1% Triton X-100 for 20 min at room temperature. Cells were blocked with 2% normal goat serum in DPBS with 1% BSA and washed with 0.1% Tween 20.
This image was generated using the ascites version of the product.
ab24609 (1/200) staininig Nuclear Pore Complex Proteins in human RPE-1 cells (green). Cells were fixed in paraformaldehyde, permeabilised with Triton X100 and counterstained with DAPI in order to highlight the nucleus (blue). Please refer to abreview for further experimental details.
This image was generated using the ascites version of the product.
ab24609 (1/500) staining Nuclear Pore Complex Proteins in human Hela Cells (green). Cells were fixed with Paraformaldehyde/Triton X-100 (10 min in PTEMF buffer (20mM PIPES, 1mM MgCl2, 10mM EGTA, 4% PFA) /0.2% Triton-X100 at room T°C) or Methanol (6 min in Methanol -20 °C , followed by 3 washes in 1x PBS) and counterstained with Dapi in order to highligh the nucleus (blue).
This image was generated using the ascites version of the product.
ab24609 (1/500) staining Nuclear Pore Complex Proteins in murine NIH/3T3 Cells (green). Cells were fixed with Paraformaldehyde/Triton X-100 (10 min in PTEMF buffer (20mM PIPES, 1mM MgCl2, 10mM EGTA, 4% PFA) /0.2% Triton-X100 at room T°C) or Methanol (6 min in Methanol -20 °C , followed by 3 washes in 1x PBS) and counterstained with Dapi in order to highligh the nucleus (blue).
This image was generated using the ascites version of the product.
HeLa cells were fixed with 4% paraformaldehyde (PFA) for 15 minutes, permeabilized with 0.5% Triton X-100 for 3 minutes, and blocked with 5% FBS for 60 minutes. Then the cells were intracellularly stained with (A) mouse IgG1, κ isotype control (Negative) or (B-D) Nuclear Pore Complex (ab24609) overnight at 4°C followed by Alexa Fluor® 647 (Red) Goat anti-Mouse IgG incubation for one hour at room temperature. The image was captured with a 60X objective using KEYENCE BZ-X700 fluorescence microscope. Exposure time (Seconds) for (A-D) is 1/5. Concentrations for (A-B) is 5 μg/ml, (C) is 2 μg/ml and (D) is 0.5 μg/ml.
IHC staining using ab24609 on formalin-fixed paraffin-embedded human tonsiltissue. The tissue was incubated with 1
μg/mL of ab24609 overnight at 4°C, followed by incubation with 2.5 μg/mL of Alexa Fluor® 647 goat anti-mouse IgG antibody (red) for one hour at room temperature. Nuclei were counterstained with DAPI (blue), and the slide was mounted with ProLong™ Gold Antifade Mounting Solution. The image was captured with a 40x objective.
Scalebar = 50 μM.
Immunofluorescence of HeLa with Nuclear Pore Complex Proteins Mouse primary antibody ab24609 at 1 µg/mL. Alexa Fluor® 594 (Red) Goat anti-Mouse IgG was used as secondary antibody. Nuclei were counterstained with DAPI (Blue).
Exposure time is 80 ms.
All lanes: Western blot - Anti-Nuclear Pore Complex Proteins antibody [Mab414] (ab24609)
Lane 1: HaCaT (Human keratinocyte cell line) cell lysate
Lane 2: Daudi (Human Burkitt's lymphoma cell line) cell lysate
Lane 3: RAW 264.7 (Mouse) cell lysate
Lane 4: UMR106 (Rat) cell lysate
All lanes: HRP Goat anti-Mouse secondary antibody
Predicted band size: 62 kDa
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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