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Read our guarantee »Products:Cell Biology >> Apoptosis >> Nucleus >> Lamins
Anti-Lamin B1 antibody [119D5-F1] - Nuclear Envelope Marker
See all Lamin B1 products (12) ...
Mouse monoclonal [119D5-F1] to Lamin B1 - Nuclear Envelope Marker
Reacts against lamin B1, does not cross react with lamin B2. Lamins do not appear to be universally distributed among different cell and tissue types. ab8982 has been shown to react with HeLa and 3T3 cells in immunocytochemistry. Other cell/tissue types have not been tested.
WB, Dot Blot, ELISA, Flow Cyt, ICCmore details
Reacts with
Mouse, Rat, Sheep, Rabbit, Cow, Human
Purified rat liver lamins
C-terminal to residue 231.
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 0.09% Sodium Azide
Constituents: PBS
Concentration information loading...
Protein G purified
Monoclonal
119D5-F1
P3x63-Ag8.653
IgG1
kappa
Signal Transduction >> Cytoskeleton / ECM >> Cytoskeleton >> Intermediate Filaments >> Class V >> Lamins
Tags & Cell Markers >> Subcellular Markers >> Nucleus >> Nuclear Envelope
Cell Biology >> Apoptosis >> Nucleus >> Lamins
Our Abpromise guarantee covers the use of ab8982 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Dot: Use at an assay dependent dilution.
ELISA: Use at an assay dependent dilution.
Flow Cyt: 1/100 - 1/200.
ICC: 1/20 - 1/50.
WB: 1/100 - 1/1000. Predicted molecular weight: 67 kDa. (see Machiels et al reference and recommended protocol).
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
Lamins are components of the nuclear lamina, a fibrous layer on the nucleoplasmic side of the inner nuclear membrane, which is thought to provide a framework for the nuclear envelope and may also interact with chromatin.
Defects in LMNB1 are the cause of leukodystrophy demyelinating autosomal dominant adult-onset (ADLD) [MIM:169500]. ADLD is a slowly progressive and fatal demyelinating leukodystrophy, presenting in the fourth or fifth decade of life. Clinically characterized by early autonomic abnormalities, pyramidal and cerebellar dysfunction, and symmetric demyelination of the CNS. It differs from multiple sclerosis and other demyelinating disorders in that neuropathology shows preservation of oligodendroglia in the presence of subtotal demyelination and lack of astrogliosis.
Belongs to the intermediate filament family.
B-type lamins undergo a series of modifications, such as farnesylation and phosphorylation. Increased phosphorylation of the lamins occurs before envelope disintegration and probably plays a role in regulating lamin associations.
Nucleus inner membrane.
Target information above from: UniProt accessionP20700
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunocytochemistry - Lamin B1 antibody [119D5-F1] - Nuclear Envelope Marker (ab8982)
![Immunocytochemistry - Lamin B1 antibody [119D5-F1] - Nuclear Envelope Marker (ab8982)](/ps/datasheet/Images/8/ab8982/ab8982_4.jpg)
Methanol fixed HeLa and 3T3 cells were stained with ab8982 (1/50 and 1/20 respectively). The cells were fixed in 100% methanol for 6 minutes at -20°C. ab8982 clearly stains the nuclear envelope with very little backgrouns staining.
A: HeLa cells + ab8982 (1/50) (green)
B: HeLa cells counterstained with DAPI (blue)
C. 3T3 cells + ab8982 (1/20) (green)
D. 3T3 cells counterstained with DAPI (blue)
Marilena Ciciarello & Patrizia Lavia, University La Sapienza
Flow Cytometry-Lamin B1 antibody [119D5-F1] - Nuclear Envelope Marker(ab8982)
![Flow Cytometry-Lamin B1 antibody [119D5-F1] - Nuclear Envelope Marker(ab8982)](/ps/datasheet/images/8/ab8982/Lamin-B1-Primary-antibodies-ab8982-3.jpg)
Overlay histogram showing HeLA cells stained with ab8982 (red line). The cells were fixed with 100% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab8982, 1µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was Mouse IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.
This product has been referenced in:
See all 10 publications for this product
Publishing research using ab8982? Please let us know so that we can cite the reference in this datasheet
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Concentration not available for this lot.
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![Immunocytochemistry - Lamin B1 antibody [119D5-F1] - Nuclear Envelope Marker (ab8982)](/ps/datasheet/Images/8/ab8982/ab8982_4.jpg)
Methanol fixed HeLa and 3T3 cells were stained with ab8982 (1/50 and 1/20 respectively). The cells were fixed in 100% methanol for 6 minutes at -20°C. ab8982 clearly stains the nuclear envelope with very little backgrouns staining.
A: HeLa cells + ab8982 (1/50) (green)
B: HeLa cells counterstained with DAPI (blue)
C. 3T3 cells + ab8982 (1/20) (green)
D. 3T3 cells counterstained with DAPI (blue)
Marilena Ciciarello & Patrizia Lavia, University La Sapienza
![Flow Cytometry-Lamin B1 antibody [119D5-F1] - Nuclear Envelope Marker(ab8982)](/ps/datasheet/images/8/ab8982/Lamin-B1-Primary-antibodies-ab8982-3.jpg)
Overlay histogram showing HeLA cells stained with ab8982 (red line). The cells were fixed with 100% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab8982, 1µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (
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