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ABT1387

Anti-Phospho-Lamin A/C (Ser404)

from rabbit

Synonym(e):

Prelamin A/C, Renal carcinoma antigen NY-REN-32

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Größe/SKUVerfügbarkeitPreis
200 μL
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€ 419,00

Über diesen Artikel

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Clone:
polyclonal
Species reactivity:
human
Application:
IF, WB, inhibition assay
Citations:
2

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biological source

rabbit

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

species reactivity

human

technique(s)

immunofluorescence: suitable, inhibition assay: suitable (peptide), western blot: suitable

isotype

IgG

NCBI accession no.

UniProt accession no.

target post-translational modification

phosphorylation (pSer404)

Gene Information

human ... LMNA(4000)

General description

Prelamin-A/C (UniProt: P02545) is encoded by the LMNA (also known as LMN1) gene (Gene ID: 4000) in human. Prelamin-A/C is subsequently cleaved into Lamin A/C. Lamins are components of the nuclear lamina that provides a framework for the nuclear envelope and interact with chromatin. Prelamin-A/C
Is cleaved to generate Lamin A/C. Farnesylation of prelamin-A/C facilitates nuclear envelope targeting and subsequent cleavage by ZMPSTE24/FACE1 to remove the farnesyl group produces mature Lamin-A/C that is inserted into the nuclear lamina. Lamin A and C are present in equal amounts in the lamina of mammals and they play an important role in nuclear assembly, chromatin organization, nuclear membrane and telomere dynamics. Lamins are shown to be essential for normal development of peripheral nervous system and skeletal muscle and for muscle satellite cell proliferation. Lamins also prevent fat infiltration of muscle and bone marrow, helping to maintain the volume and strength of skeletal muscle and bone. Phosphorylation of Lamins is reported to occur continuously throughout all interphase periods and takes place mainly on the assembled lamina. Phosphorylation of the major polypeptides of the lamina induces laminar disassembly during mitosis. Phosphorylated Lamin-A/C localizes to nucleoplasm. Lamin A/C undergoes phosphorylation at multiple sites and one of the best characterized phosphorylation sites is on Serine 22 and it is phosphorylated during interphase. Phosphorylation of Serine 22 stabilizes Lamin A/C. Overexpression of Lamin-A is shown to result in greater phosphorylation of Serine 22 and 390 and Lamin A/C knockdowns display reduced phosphorylation at both sites, which helps in maintaining the integrity of the diminished lamina. Lamin A/C can undergoes phosphorylation on Serine 404 by Akt1 and Ser4040 phosphorylated Lamin undergoes rapid lysosomal degradation. Mutations in LMNA gene can cause Emery-Dreifuss muscular dystrophy 2 and 3, which are characterized by weakness and atrophy of muscle without involvement of the nervous system and cardiac conduction defects. Some mutations have also been linked to familial Lipodystrophy that leads to the loss of subcutaneous adipose tissue in the lower parts of the body and accumulation of adipose tissue in the face and neck. (Ref.: Buxboim, A., et al. (2014). Curr. Biol. 24(16): 1909-1917; Toker, A., and Marmiroli, S. (2014). Adv. Biol. Regul. 55: 28-38).
~75 kDa and 65 kDa observed; 74.14 and 65.14 kDa calculated for Lamin A and C, respectively. Uncharacterized bands may be observed in some lysate(s).

Immunogen

Epitope: unknown
KLH-conjugated linear peptide corresponding to 12 amino acids from human Lamin A/C surrounding phosphorylated Serine 404.

Application

Anti-Phospho-Lamin A/C (Ser404), Cat. No. ABT1387, is a rabbit polyclonal antibody that detects Lamin A/C phosphorylated on Serine 404 and has been tested for use in Immunofluorescence, Western Blotting, and Peptide Inhibition Assay.
Immunofluorescence Analysis: 0.2 µg/mL from a representative lot detected Phospho-Lamin A/C (Ser404) in A549 lung carcinoma cells. (Courtesy of Sangkyun Cho & Dr. D.E Discher at University of Pennsylvania).

Peptide Inhibition Analysis: A 1:500 dilution from a representative lot was used with A549 cells (specific for Lamin A/C phosphorylation) for peptide block analysis.
Research Category
Cell Structure

Biochem/physiol Actions

This rabbit polyclonal antibody detects human Lamin A/C phosphorylated on Serine 404.

Physical form

Affinity Purified
Format: Purified
Purified rabbit polyclonal antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Preparation Note

Stable for 1 year at 2-8°C from date of receipt.

Analysis Note

Evaluated by Western Blotting in A549 cells.

Western Blotting Analysis: A 1:500 dilution of this antibody detected Phospho-Lamin A/C (Ser404) in A549 cells (specific for Lamin A/C phosphorylation).

Other Notes

Concentration: Please refer to lot specific datasheet.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Dieser Artikel
MABT1341HPA006660MABT1458
description

from rabbit

description

clone 4C11, from mouse

description

affinity isolated antibody, buffered aqueous glycerol solution

description

-

biological source

rabbit

biological source

mouse

biological source

rabbit

biological source

rat

antibody form

affinity isolated antibody

antibody form

purified immunoglobulin

antibody form

affinity isolated antibody

antibody form

purified antibody

species reactivity

human

species reactivity

human, monkey, Syrian hamster, rat, mouse

species reactivity

human

species reactivity

mouse

clone

polyclonal

clone

4C11, monoclonal

clone

polyclonal

clone

3C8, monoclonal

UniProt accession no.

P02545

UniProt accession no.

P02545

UniProt accession no.

P02545

UniProt accession no.

P48678

technique(s)

inhibition assay: suitable (peptide), immunofluorescence: suitable, western blot: suitable

technique(s)

ChIP: suitable, immunoprecipitation (IP): suitable, western blot: suitable, immunofluorescence: suitable

technique(s)

immunoblotting: 0.04-0.4 μg/mL, immunohistochemistry: 1:50-1:200

technique(s)

immunofluorescence: suitable, western blot: suitable, immunocytochemistry: suitable, immunohistochemistry (frozen sections): suitable


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Lagerklasse

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



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