
Phospho-Lamin A/C (Ser392) Rabbit Polyclonal Antibody#abs130684
Dear customers, please note that the mentioned price is solely for reference purposes. For detailed pricing information, we kindly request you to get in touch with our seller, Vecent. Data Examples Western blot analysis on COS7 cell lysate using Histone H1 Antibody This product is for research...
Description
Catalog-specification | Delivery time | USD price |
abs130684-50ug | 1-2 Weeks | 201 |
abs130684-100ug | 1-2 Weeks | 301 |
Dear customers, please note that the mentioned price is solely for reference purposes. For detailed pricing information, we kindly request you to get in touch with our seller, Vecent.
Overview | |
Description | The inner nuclear membrane is flanked by a two-dimensional matrix of proteins known as the nuclear lamina. This matrix is primarily composed of the lamin family of proteins, which have remarkably high levels of conservation throughout evolution. One crucial aspect of the lamina matrix is its ability to undergo reversible disassembly during mitosis. This disassembly occurs when the lamin proteins undergo phosphorylation, leading to dynamic changes in the nuclear structure. |
Other names | Lamin A/C, also known as LMNA, is a protein that plays an important role in various cellular processes, including DNA replication, transcription, and chromatin organization. It is encoded by the LMNA gene and has a molecular weight of 70 kDa. |
Source | Rabbit |
Specificity | The detection of Lamin A/C protein requires the presence of phosphorylation at Serine 392. This antibody specifically targets and recognizes endogenous levels of Lamin A/C that have undergone phosphorylation at this site. By analyzing the phosphorylation status at Serine 392, the antibody enables the identification of Lamin A/C protein in various biological samples. It is important to note that this antibody does not detect the non-phosphorylated form of Lamin A/C. |
| Reactivity | Human;Mouse;Rat |
Predictive reaction species | Zebrafish;Pig;Rabbit;Horse;Bovine |
| Antigen | Lamin A/C |
Application | We recommend using the following dilutions for different applications: Western blot (WB) at 1:500-1:2000, immunohistochemistry (IHC) at 1:50-1:1000, immunofluorescence/immunocytochemistry (IF/ICC) at 1:100-1:500, and enzyme-linked immunosorbent assay (ELISA) using peptide at 1:20000-1:40000. |
| Immunogen | 。,Lamin A/C392。 |
Properties | |
| MW | 74,65kDa |
| Concentration | 1mg/ml |
Purification | The purification process of the antibody involves affinity purification using phospho- and non-phospho-peptide affinity columns on purified rabbit serum. By sequentially conducting chromatography on these columns, the antibody is obtained. |
Clonality | Polyclonal Antibody |
| Stability & Storage | To ensure the preservation of the item, store it at a temperature of -20 °C for a period of one year. It is important to avoid subjecting it to repeated freeze/thaw cycles. |
Storage buffer | The Rabbit IgG is stored in a solution containing phosphate buffered saline, with a pH of 7.4, 150mM NaCl, 0.02% sodium azide, and 50% glycerol. It should be kept at a temperature of -20°C, and can remain stable for up to 12 months from the date of receipt. It is important to note that any attempts to modify the contents of this storage solution may result in changes to the properties or effectiveness of the product. Therefore, it is recommended that this solution be used as is, without any alterations. |
Target | |
Background | 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 A and C are present in equal amounts in the lamina of mammals. Plays an important role in nuclear assembly, chromatin organization, nuclear membrane and telomere dynamics. Required for normal development of peripheral nervous system and skeletal muscle and for muscle satellite cell proliferation. Required for osteoblastogenesis and bone formation. Also prevents fat infiltration of muscle and bone marrow, helping to maintain the volume and strength of skeletal muscle and bone. |
Tissue specificity | In the arteries, prelamin-A/C accumulation is not observed in young healthy vessels but is prevalent in medial vascular smooth muscle cells (VSMCs) from aged individuals and in atherosclerotic lesions, where it often colocalizes with senescent and degenerate VSMCs. Prelamin-A/C expression increases with age and disease. In normal aging, the accumulation of prelamin-A/C is caused in part by the down-regulation of ZMPSTE24/FACE1 in response to oxidative stress. |
| Posttranslational modification | Increased phosphorylation of the lamins occurs before envelope disintegration and probably plays a role in regulating lamin associations.Proteolytic cleavage of the C-terminal of 18 residues of prelamin-A/C results in the production of lamin-A/C. The prelamin-A/C maturation pathway includes farnesylation of CAAX motif, ZMPSTE24/FACE1 mediated cleavage of the last three amino acids, methylation of the C-terminal cysteine and endoproteolytic removal of the last 15 C-terminal amino acids. Proteolytic cleavage requires prior farnesylation and methylation, and absence of these blocks cleavage.Sumoylation is necessary for the localization to the nuclear envelope.Farnesylation of prelamin-A/C facilitates nuclear envelope targeting. |
Celluar localization | Cytoskeleton;Cytosol;Extracellular region or secreted;Nucleus; |
| UniPort | P02545 |
Data Examples

Western blot analysis on COS7 cell lysate using Histone H1 Antibody
This product is for research use only, not for use in diagnostic prodecures or in human.
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