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Proteins and peptidesAnti-Ly6g antibody [1A8] - mouse IgG2c (Chimeric)
Low endotoxin, Azide free.
Our first-to-market chimera with mouse IgG2c backbone, this functional antibody specifically depletes neutrophils in vivo for up to 72h.
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Rabbit anti-Lamin B1 antibody ab16048 is a rabbit polyclonal antibody that is used in Lamin B1 western blotting, IHC and immunofluorescence. Suitable for human, mouse and rat samples.
Tried and trusted by researchers since 2005
Specificity confirmed with LMNB1 knockout cell line validation
Anti-Lamin B1 antibody ab16048 is cited in over 1270 publications
Same trusted quality, New lower price!
IgG
Rabbit
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 98.98% PBS, 1% BSA
Liquid
Polyclonal
ICC/IF | WB | IHC-P | |
---|---|---|---|
Human | Tested | Tested | Tested |
Mouse | Expected | Tested | Expected |
Rat | Expected | Tested | Expected |
Chicken | Predicted | Predicted | Predicted |
Indian muntjac | Predicted | Predicted | Predicted |
Pig | Predicted | Predicted | Predicted |
Xenopus laevis | Predicted | Predicted | Predicted |
Zebrafish | Predicted | Predicted | Predicted |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 0.1 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info - | Notes - |
Species Mouse | Dilution info 0.1 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Chicken, Pig, Xenopus laevis, Indian muntjac, Zebrafish | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 0.1 µg/mL | Notes We recommend Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773). |
Species Mouse | Dilution info 0.1 µg/mL | Notes We recommend Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773). |
Species Rat | Dilution info 0.1 µg/mL | Notes We recommend Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773). |
Species | Dilution info | Notes |
---|---|---|
Species Chicken, Pig, Xenopus laevis, Indian muntjac, Zebrafish | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 0.1-1 µg/mL | Notes Perform heat-mediated antigen retrieval before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Chicken, Pig, Xenopus laevis, Indian muntjac, Zebrafish | Dilution info - | Notes - |
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.
Lamin-B1, LMNB, LMN2, LMNB1
Rabbit anti-Lamin B1 antibody ab16048 is a rabbit polyclonal antibody that is used in Lamin B1 western blotting, IHC and immunofluorescence. Suitable for human, mouse and rat samples.
Tried and trusted by researchers since 2005
Specificity confirmed with LMNB1 knockout cell line validation
Anti-Lamin B1 antibody ab16048 is cited in over 1270 publications
Same trusted quality, New lower price!
Lamin-B1, LMNB, LMN2, LMNB1
IgG
Rabbit
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 98.98% PBS, 1% BSA
Liquid
Polyclonal
Affinity purification Immunogen
From July 2024, QC testing of replenishment batches of this polyclonal changed. All tested and expected application and reactive species combinations are still covered by our Abcam product promise. However, we no longer test all applications. For more information on a specific batch, please contact our Scientific Support who will be happy to help.
Blue Ice
1-2 weeks
+4°C
-20°C
Upon delivery aliquot
Avoid freeze / thaw cycle
Lamin B1 and Lamin B antibodies are extremely useful as nuclear loading controls for use with nuclear extracts. When using Lamin B1 antibodies as nuclear loading controls, be aware that in apoptotic cells Lamin B1 is cleaved (Kottke TJ et al.). Lamin B1 will also be removed from a nuclear prep if the nuclear membranes are spun out. This antibody was designed to be a nuclear loading control however it has not yet been tested in appropriate lysates.
Abcam is leading the way to address reproducibility in scientific research with our highly validated recombinant monoclonal and recombinant multiclonal antibodies. Search & select one of Abcam's thousands of recombinant alternatives to eliminate batch-variability and unnecessary animal use.
If you do not find a host species to meet your needs, our catalogue and custom Chimeric range provides scientists the specificity of Abcam's RabMAbs in the species backbone of your choice. Remember to also review our range of edited cell lines, proteins and biochemicals relevant to your target that may help you further your research goals.
Abcam antibodies are extensively validated in a wide range of species and applications, so please check the reagent specifications meet your scientific needs before purchasing. If you have any questions or bespoke requirements, simply visit the Contact Us page to send us an inquiry or contact our Support Team ahead of purchase.
The Lamin B1 protein supports nuclear stability and regulates chromatin organization. It is a component of the nuclear lamina complex interacting with other lamin proteins such as lamin A and lamin C to form a structured network. This network is essential for chromatin tethering and gene expression regulation influencing cellular processes at the transcriptional level. Its interactions with chromatin and other nuclear components highlight its significance in the overall functional architecture of the cell nucleus.
Lamin B1 also known as LMNB1 is a protein component of the nuclear lamina a dense fibrillar network inside the nuclear envelope. It plays a critical structural role in maintaining nuclear integrity. Lamin B1 typically has a molecular weight of approximately 67 kDa. This protein is expressed in the cells of almost all tissues contributing to the maintenance and organization of the nuclear envelope. Researchers often use Western blot techniques to detect and analyze Lamin B1 size and expression levels in various biological samples.
Lamin B1 interacts with molecules involved in the mitotic spindle assembly and DNA replication pathways. It plays an essential role in mitosis where it helps in the disassembly and reassembly of the nuclear envelope. Lamin B1’s interactions with proteins like lamin A/C and emerin highlight its participation in nuclear membrane dynamics and chromatin organization during the cell cycle.
Abnormalities in Lamin B1 levels or function associate with conditions like autosomal dominant leukodystrophy and certain types of cancer. Misregulation or mutation of LMNB1 can alter nuclear stability and gene expression contributing to disease pathology. Lamin B1 also connects with proteins like emerin where the disrupted interaction may lead to nuclear envelope-related muscular dystrophies. Understanding these connections is vital for elucidating the molecular basis of these diseases.
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.
All lanes: Western blot - Anti-Lamin B1 antibody - Nuclear Envelope Marker (AB16048) at 1/1000 dilution
All lanes: Human Pancreatic cell line - whole cell lysate at 20 µg
All lanes: HRP conjugated goat anti-rabbit antibody at 1/2000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 66 kDa
Observed band size: 68 kDa
Exposure time: 30s
Blocking buffer: 3% Milk
Gel type: MOPS
Exposure Time: 2 minutes
Observed band size: 73 kDa
Additional bands: 46 kDa
All lanes: Western blot - Anti-Lamin B1 antibody - Nuclear Envelope Marker (AB16048) at 1 µg/mL
Lane 1: HeLa whole cell lysate at 10 µg
Lane 2: PC12 whole cell lysate at 10 µg
Lane 3: NIH 3T3 whole cell lysate at 10 µg
All lanes: Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/50000 dilution
Predicted band size: 66 kDa
Lane 1: Wild type HAP1 whole cell lysate (20 μg)
Lane 2: empty lane
Lane 3: KO HAP1 LMNB1 whole cell lysate (20 μg)
Lane 4: empty lane
Lanes 1 - 4: Merged signal (red and green). Green - ab16048 observed at 70 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab16048 was shown to specifically react with LMNB1 (Lamin B1) in wild type HAP1 cells. No band was observed when LMNB1 (Lamin B1) knockout samples were used. Ab16048 LMNB1 (Lamin B1) and ab8245 (Mouse anti GAPDH loading control) were incubated overnight at 4°C at 0.1 μg per mL and 1/10000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (ab216776) secondary antibodies at 1/10000 dilution for 1 hour at room temperature before imaging.
All lanes: Western blot - Anti-Lamin B1 antibody - Nuclear Envelope Marker (AB16048)
Predicted band size: 66 kDa
ab16048 staining Lamin B1 in HepG2 cells. The cells were fixed with 4% paraformaldehyde (10 min), permeabilized with 0.1% PBS-Triton X-100 for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1%PBS-Tween for 1h. The cells were then incubated overnight at 4°C with ab16048 at 0.1µg/ml and ab7291, Mouse monoclonal [DM1A] to alpha Tubulin - Loading Control. Cells were then incubated with ab150081, Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (Alexa Fluor® 488), pre-adsorbed at 1/1000 dilution (shown in green) and ab150120, Goat polyclonal Secondary Antibody to Mouse IgG - H&L (Alexa Fluor® 594), pre-adsorbed at 1/1000 dilution (shown in pseudocolour red). Nuclear DNA was labelled with DAPI (shown in blue).
Also suitable in cells fixed with 100% methanol (5 min).
Image was acquired with a high-content analyser (Operetta CLS, Perkin Elmer) and a maximum intensity projection of confocal sections is shown.
IHC image of Lamin B1 staining in Human normal Liver formalin fixed paraffin embedded tissue section*, performed on a Leica Bond™ system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab16048, 1μg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
*Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre
Lane 1: Wild-type HAP1 nuclear lysate (10 μg)
Lane 2: Lamin B1 knockout HAP1 nuclear lysate (10 μg)
Lanes 1 and 2: Green signal from target - ab16048 observed at 68 kDa. Red signal from loading control - ab10799 observed at 18 kDa.
ab16048 was shown to specifically react with lamin B1 in wild-type HAP1 cells. No band was observed knockout samples were used. Wild-type and lamin B1 knockout samples were subjected to SDS-PAGE. ab16048 and ab10799 (loading control to histone H3 at 0.1μg/mL) were both incubated overnight at 4°C. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (ab216776) secondary antibodies at 1/10,000 dilution for 1 h at room temperature before imaging.
All lanes: Western blot - Anti-Lamin B1 antibody - Nuclear Envelope Marker (AB16048) at 1 µg/mL
Lane 1: Wild-type HAP1 nuclear lysate at 10 µg
Lane 2: Lamin B1 knockout HAP1 nuclear lysate at 10 µg
All lanes: Western blot - Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (AB216773) at 1/10000 dilution
Performed under reducing conditions.
Predicted band size: 36 kDa, 66 kDa
Observed band size: 68 kDa
All lanes: Western blot - Anti-Lamin B1 antibody - Nuclear Envelope Marker (AB16048) at 1/1000 dilution
All lanes: HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysate at 20 µg
All lanes: Alexa fluor goat polyclonal to Rabbit IgG at 1/10000 dilution
Performed under reducing conditions.
Predicted band size: 66 kDa
Observed band size: 68-70 kDa
ab16048 staining Lamin B1 in human infantile fibromatosis tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Tissue was fixed with formaldehyde and blocked with 1% FBS/BSA for 3 hours at room temperature; antigen retrieval was by heat mediation in Tris pH9. Samples were incubated with primary antibody (1/100 in TBS + 1% BSA + 1% FBS) for 16 hours. An undiluted HRP-conjugated goat anti-rabbit IgG polyclonal was used as the secondary antibody.
Human and mouse cells stained with ab16048 (1/500). The cells were fixed and permeabilized in 4% formaldehyde, 0.2% Tritonm X100 for 10 minutes at room temperature, then washed 3x in PBS.
A: HeLa cells + ab16048 (green)
B: HeLa cells counterstained with DAPI (blue)
C: 3T3 cells + ab16048 (green)
D: 3T3 cells counterstained with DAPI (blue)
Human and mouse cells stained with ab16048 (1/500). The cells were fixed in 100% methanol for 6 minutes at -20°C, then washed once in PBS.
A: HeLa cells + ab16048 (green)
B: HeLa cells counterstained with DAPI (blue)
C: 3T3 cells + ab16048 (green)
D: 3T3 cells counterstained with DAPI (blue)
Immunohistochemical analysis of formalin-fixed paraffin-embedded human liver labelling lamin B1 with ab16048 at a concentration of 0.2µg/ml. The immunostaining was performed on a Ventana DISCOVERY ULTRA (Roche Tissue Diagnostics) instrument with an OptiView DAB IHC Detection Kit. Heat mediated antigen retrieval was conducted for 32min with ULTRA cell conditioning solution (CC1 pH8.5). ab16048 anti lamin B1 antibody was incubated at 37°C for 16min. Sections were counterstained with Hematoxylin II. Image inset shows absence of staining in secondary antibody only control.
Immunocytochemistry analysis of formaldehyde-fixed NP40-permeabilized Mouse vascular smooth muscle cells staining with ab16048 at 1/100. Secondary antibody was Alexa Fluor® 488 donkey Anti-rabbit at 1/500 dilution. Samples were incubated with the primary antibody with 3% BSA in PBS for 12 hours at 4°C. Blocking was done using 3% BSA for 1 hour at 21°C.
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