Immunofluorescent analysis of HeLa cells stained with panspecificmouse mAb to the nuclear pore complex (NPC), MCA-39C7, dilution 1:100 in red, and costained with chicken pAb to vimentin, <a href="http://encorbio.com/products/cpca-vim/">CPCA-Vim</a>, dilution 1:10,000, in green. The blue is DAPI staining of nuclear DNA. The MCA-39C7 antibody reveals strong granular staining of the nuclei corresponding to the NPC, while the CPCA-Vim antibody specifically labels intermediate filaments in these cell
Immunofluorescent analysis of HeLa cells stained with panspecificmouse mAb to the nuclear pore complex (NPC), MCA-39C7, dilution 1:100 in red, and costained with chicken pAb to vimentin, <a href="http://encorbio.com/products/cpca-vim/">CPCA-Vim</a>, dilution 1:10,000, in green. The blue is DAPI staining of nuclear DNA. The MCA-39C7 antibody reveals strong granular staining of the nuclei corresponding to the NPC, while the CPCA-Vim antibody specifically labels intermediate filaments in these cell

EnCor Biotechnology

Pan Specific Nuclear Pore Complex Mouse Monoclonal Antibody Cat# MCA-39C7

$250.00
Description

      The MCA-39C7 was made against a yeast nuclear preparation and proved to bind nuclear pore complexes by IF on yeast cells. When this antibody was tested on cells from other species, including rat, mouse and human cells, it has invariably strongly stained nuclear pore complexes, so it appears to bind to a highly conserved epitope and therefore to be an excellent and useful panspecific marker for these important structures. On western blots of mammalian cells it binds to a ~62kDa protein and some higher molecular weight bands. We are currently unsure of the exact identity of these proteins, and work is in progress to to identify them. We note that the Mab 414 antibody described by Davis and Blobel has very similar properties (3).

Amount: 500µL of hybridoma culture media
Amount: 500µL of hybridoma culture media
Immunofluorescent analysis of HeLa cells stained with panspecificmouse mAb to the nuclear pore complex (NPC), MCA-39C7, dilution 1:100 in red, and costained with chicken pAb to vimentin, CPCA-Vim, dilution 1:10,000, in green. The blue is DAPI staining of nuclear DNA. The MCA-39C7 antibody reveals strong granular staining of the nuclei corresponding to the NPC, while the CPCA-Vim antibody specifically labels intermediate filaments in these cells.
Western blot analysis of different cell lysates, cytosol or nuclear enriched fractions using pan-specific mouse mAb to the nuclear pore complex (NPC), MCA-39C7, dilution 1:100 in green: [1] protein standard (red), [2] HEK293 cytosol, [3] HEK293 nuclear, [4] NIH-3T3 cytosol, [5] NIH-3T3 nuclear, [6] HeLa cytosol, and [7] HeLa nuclear fraction lysate. The band at about 68kDa represents a currently unidentified NPC protein which is detected predominantly in the nuclear enriched fractions of all cell lines.

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Name: Panspecific Nuclear Pore Complex, mouse monoclonal, Cat# MCA-39C7
Immunogen: Yeast nuclear preparations
Molecular Weight: ~62kDa
Host: Mouse
Isotype: IgG1
Species Cross-Reactivity: Human, rat, mouse, cow, pig, horse, chicken, Drosophila, Caenorhabditis, Yeast
RRID: AB_2186243
Format: Concentrated hybridoma cell culture media supernatant plus 5mM NaN3
Applications: WB, IF/ICC, IHC
Recommended Dilutions: WB: 1:100, IF/ICC: 1:100-1:500 (yeast cells), 1:50-1:100 (mammalian cells). IHC: 1:2
Storage: Store at 4°C for short term, for longer term at -20°C. Avoid freeze/thaw cycles.

      Nuclear pores form a barrier between the nucleus and cytoplasm in eukaryotic cells allowing regulated inflow and egress of proteins and RNA. They are composed of a family of nuclear pore proteins called nucleoporins with about 30 members in humans (1,2). This monoclonal antibody was raised by injecting mice with crude yeast nuclear preparations and screening the resulting hybridomas by immunofluorescence on yeast cells. The MCA-39C7 clone produced antibody which was one of several which strongly and specifically labelled nuclear pore complexes. When this antibody was tested on cells from other species, including rat, mouse and human cells, it has invariably strongly stained nuclear pore complexes, so it appears to bind to a highly conserved epitope and there to be an excellent and useful panspecific marker for these important structures.



      Chromogenic Immunostaining of a NBF fixed paraffin embedded human brain cortex section with mouse mAb to the nuclear pore complex, MCA-39C7 supernatant, dilution 1:2, detected in DAB (brown) following the ImmPress method with citra buffer retrieval. Hematoxylin (blue) was used as the counterstain. The nuclear pore complex antibody labels nuclei in a granular pattern that concentrates at the nuclear membrane. This antibody performs well in testing with both 4% PFA and standard NBF fixed tissues. Mouse select image for larger view.

1. Cronshaw JM, et al. Proteomic analysis of the mammalian nuclear pore complex. J. Cell Biol.158:915-27 (2002).
2. Alber F, et al. The molecular architecture of the nuclear pore complex. Nature 450:695-701 (2007).
3. Davis LI, Blobel G. Identification and characterization of a nuclear pore complex protein. Cell 45:699-709 (1986).

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