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  • Validé par KD/KO

Anticorps Polyclonal de lapin anti-Lamin A/C

Lamin A/C Polyclonal Antibody for FC, IF, IHC, IP, WB, ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain, rat, souris et plus (2)

Applications

WB, IP, IHC, IF, FC, ELISA

Conjugaison

Non conjugué

N° de cat : 10298-1-AP

Synonymes

70 kDa lamin, CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL, FPLD, HGPS, IDC, lamin A, lamin A/C, LDP1, LFP, LGMD1B, LMN1, LMNA, LMNC, Prelamin A/C, PRO1, progerin


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  • Western Blot (WB) analysis of various lysates using Lamin A/C Polyclonal antibody (10298-1-AP)

    WB analysis using 10298-1-AP

    Various lysates were subjected to SDS PAGE followed by western blot with 10298-1-AP (Lamin A/C antibody) at dilution of 1:6000 incubated at room temperature for 1.5 hours.

  • Western Blot (WB) analysis of various lysates using Lamin A/C Polyclonal antibody (10298-1-AP)

    WB analysis using 10298-1-AP

    Various lysates were subjected to SDS PAGE followed by western blot with 10298-1-AP (Lamin A/C antibody) at dilution of 1:35000 incubated at room temperature for 1.5 hours.

  • Western Blot (WB) analysis of HeLa cells using Lamin A/C Polyclonal antibody (10298-1-AP)

    WB analysis of HeLa using 10298-1-AP

    WB result of Lamin A/C antibody (10298-1-AP; 1:20000; incubated at room temperature for 1.5 hours) with sh-Control and sh-Lamin A/C transfected HeLa cells.

  • Western Blot (WB) analysis of C6 cells using Lamin A/C Polyclonal antibody (10298-1-AP)

    WB analysis of C6 using 10298-1-AP

    C6 cells were subjected to SDS PAGE followed by western blot with 10298-1-AP (Lamin A/C Antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours.

  • Western Blot (WB) analysis of HEK-293 cells using Lamin A/C Polyclonal antibody (10298-1-AP)

    WB analysis of HEK-293 using 10298-1-AP

    HEK-293 cells were subjected to SDS PAGE followed by western blot with 10298-1-AP (lamin-A antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours.

  • Western Blot (WB) analysis of A375 cells using Lamin A/C Polyclonal antibody (10298-1-AP)

    WB analysis of A375 using 10298-1-AP

    A375 cells were subjected to SDS PAGE followed by western blot with 10298-1-AP (lamin-A antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours.

  • Western Blot (WB) analysis of mouse ovary tissue using Lamin A/C Polyclonal antibody (10298-1-AP)

    WB analysis of mouse ovary using 10298-1-AP

    mouse ovary tissue were subjected to SDS PAGE followed by western blot with 10298-1-AP (lamin-A antibody) at dilution of 1:800 incubated at room temperature for 1.5 hours.

  • Western Blot (WB) analysis of SKOV-3 cells using Lamin A/C Polyclonal antibody (10298-1-AP)

    WB analysis of SKOV-3 using 10298-1-AP

    SKOV-3 cells were subjected to SDS PAGE followed by western blot with 10298-1-AP (lamin-A antibody) at dilution of 1:800 incubated at room temperature for 1.5 hours.

  • Immunoprecipitation (IP) experiment of HeLa cells using Lamin A/C Polyclonal antibody (10298-1-AP)

    IP experiment of HeLa using 10298-1-AP

    IP result of anti-Lamin A/C(IP:10298-1-AP, 4ug; Detection:10298-1-AP 1:50000) with HeLa cells lysate 1360 ug.

  • Immunoprecipitation (IP) experiment of A375 cells using Lamin A/C Polyclonal antibody (10298-1-AP)

    IP experiment of A375 using 10298-1-AP

    IP Result of anti-lamin-A (IP:10298-1-AP, 3ug; Detection:10298-1-AP 1:1000) with A375 cells lysate 800ug.

  • Immunohistochemistry (IHC) staining of mouse heart tissue using Lamin A/C Polyclonal antibody (10298-1-AP)

    IHC staining of mouse heart using 10298-1-AP

    Immunohistochemical analysis of paraffin-embedded mouse heart tissue slide using 10298-1-AP (Lamin A/C antibody) at dilution of 1:4000 (under 10x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

  • Immunohistochemistry (IHC) staining of mouse heart tissue using Lamin A/C Polyclonal antibody (10298-1-AP)

    IHC staining of mouse heart using 10298-1-AP

    Immunohistochemical analysis of paraffin-embedded mouse heart tissue slide using 10298-1-AP (Lamin A/C antibody) at dilution of 1:4000 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

  • Immunofluorescence (IF) / fluorescent staining of HepG2 cells using Lamin A/C Polyclonal antibody (10298-1-AP)

    IF Staining of HepG2 using 10298-1-AP

    Immunofluorescent analysis of (-20℃ Ethanol) fixed HepG2 cells using 10298-1-AP (Lamin A/C antibody) at dilution of 1:200 and Alexa Fluor 488-conjugated AffiniPure Goat Anti-Rabbit IgG(H+L).

  • Immunofluorescence (IF) / fluorescent staining of HepG2 cells using Lamin A/C Polyclonal antibody (10298-1-AP)

    IF Staining of HepG2 using 10298-1-AP

    Immunofluorescent analysis of (-20°C Ethanol) fixed HepG2 cells using Lamin A/C antibody (10298-1-AP) at dilution of 1:800 and CoraLite®488-Conjugated AffiniPure Goat Anti-Rabbit IgG(H+L), CL594-Phalloidin (red).

  • Immunofluorescence (IF) / fluorescent staining of HepG2 cells using Lamin A/C Polyclonal antibody (10298-1-AP)

    IF Staining of HepG2 using 10298-1-AP

    Immunofluorescent analysis of (-20℃ Ethanol) fixed HepG2 cells using 10298-1-AP (Lamin A/C antibody) at dilution of 1:100 and Alexa Fluor 488-conjugated AffiniPure Goat Anti-Rabbit IgG(H+L).

  • Immunofluorescence (IF) / fluorescent staining of HeLa cells using Lamin A/C Polyclonal antibody (10298-1-AP)

    IF Staining of HeLa using 10298-1-AP

    Immunofluorescent analysis of (-20°C Acetone) fixed HeLa cells using 10298-1-AP (Lamin A/C antibody) at dilution of 1:100 and CL594-66467 (CL594-Mouse anti-Rabbit IgG heavy chain) as secondary antibody with dilution 1:400. .

  • Flow cytometry (FC) experiment of HEK-293T cells using Lamin A/C Polyclonal antibody (10298-1-AP)

    FC experiment of HEK-293T using 10298-1-AP

    1X10^6 HEK-293T cells were intracellularly stained with 0.4 ug Anti-Human Lamin A/C (10298-1-AP) and CoraLite®488-Conjugated AffiniPure Goat Anti-Rabbit IgG(H+L) at dilution 1:1000 (red), or 0.4 ug Isotype Control. Cells were fixed and permeabilized with Transcription Factor Staining Buffer Kit (PF00011).

"Lamin A/C Antibodies" Comparison

View side-by-side comparison of Lamin A/C antibodies from other vendors to find the one that best suits your research needs.

Applications testées

Résultats positifs en WBcellules A431, cellules A375, cellules C6, cellules HEK-293, cellules HeLa, cellules HUVEC, cellules NIH/3T3, cellules SKOV-3, tissu ovarien de souris
Résultats positifs en IPcellules HeLa, cellules A375
Résultats positifs en IHCtissu cardiaque de souris,
il est suggéré de démasquer l'antigène avec un tampon de TE buffer pH 9.0; (*) À défaut, 'le démasquage de l'antigène peut être 'effectué avec un tampon citrate pH 6,0.
Résultats positifs en IFcellules HepG2, cellules HeLa
Résultats positifs en cytométriecellules HEK-293T

Dilution recommandée

ApplicationDilution
Western Blot (WB)WB : 1:5000-1:50000
Immunoprécipitation (IP)IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
Immunohistochimie (IHC)IHC : 1:2000-1:8000
Immunofluorescence (IF)IF : 1:400-1:1600
Flow Cytometry (FC)FC : 0.40 ug per 10^6 cells in a 100 µl suspension
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, check data in validation data gallery

Informations sur le produit

10298-1-AP cible Lamin A/C dans les applications de WB, IP, IHC, IF, FC, ELISA et montre une réactivité avec des échantillons Humain, rat, souris

Réactivité Humain, rat, souris
Réactivité citéerat, Humain, singe, souris, duck
Hôte / Isotype Lapin / IgG
Clonalité Polyclonal
Type Anticorps
Immunogène Lamin A/C Protéine recombinante Ag0408
Nom complet lamin A/C
Masse moléculaire calculée 65 kDa
Poids moléculaire observé 65 kDa, 70 kDa
Numéro d’acquisition GenBankBC003162
Symbole du gène LMNA
Identification du gène (NCBI) 4000
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par affinité contre l'antigène
Tampon de stockage PBS avec azoture de sodium à 0,02 % et glycérol à 50 % pH 7,3
Conditions de stockageStocker à -20°C. Stable pendant un an après l'expédition. L'aliquotage n'est pas nécessaire pour le stockage à -20oC Les 20ul contiennent 0,1% de BSA.

Informations générales

Lamin A/C is also named as LMNA or LMN1. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated. Lamin proteins are thought to be involved in nuclear stability, chromatin structure, and gene expression. The lack of lamin A/C can be as a novel marker for undifferentiated embryonic stem cells and lamin A/C expression is an early indicator of differentiation (PMID: 16179429). Mutations in this gene lead to several diseases: Emery-Dreifuss muscular dystrophy, familial partial lipodystrophy, limb-girdle muscular dystrophy, dilated cardiomyopathy, Charcot-Marie-Tooth disease, and Hutchinson-Gilford progeria syndrome. This protein has 4 isoforms produced by alternative splicing with the molecular weight of 74 kDa, 65 kDa, 70 kDa, and 64 kDa. This antibody can recognize 4 isoforms of Lamin A/C.

Protocole

Product Specific Protocols
WB protocol for Lamin A/C antibody 10298-1-APDownload protocol
IHC protocol for Lamin A/C antibody 10298-1-APDownload protocol
IF protocol for Lamin A/C antibody 10298-1-APDownload protocol
IP protocol for Lamin A/C antibody 10298-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanIF

Nat Microbiol

Nuclear pore blockade reveals that HIV-1 completes reverse transcription and uncoating in the nucleus.

Authors - Adarsh Dharan
humanWB

Mol Cell

Lactylation-driven METTL3-mediated RNA m6A modification promotes immunosuppression of tumor-infiltrating myeloid cells.

Authors - Jia Xiong
humanWB

J Extracell Vesicles

Extracellular vesicles derived from oesophageal cancer containing P4HB promote muscle wasting via regulating PHGDH/Bcl-2/caspase-3 pathway.

Authors - Xiaohan Gao
humanWB

Cancer Cell

SET1A-Mediated Mono-Methylation at K342 Regulates YAP Activation by Blocking Its Nuclear Export and Promotes Tumorigenesis.

Authors - Lan Fang
humanWB

Sci Adv

XAF1 promotes anti-RNA virus immune responses by regulating chromatin accessibility

Authors - Ming Kuang
humanWB

Autophagy

SDC1-dependent TGM2 determines radiosensitivity in glioblastoma by coordinating EPG5-mediated fusion of autophagosomes with lysosomes

Authors - Wang Zheng

Avis

The reviews below have been submitted by verified Proteintech customers who received an incentive forproviding their feedback.


FH

Alejandro (Verified Customer) (08-22-2022)

Shows clear staining in IF and well staining using FACS

  • Applications: Immunofluorescence, Flow Cytometry
  • Primary Antibody Dilution: 1/100
  • Cell Tissue Type: Bone marrow derived macrophages
Lamin A/C Antibody Immunofluorescence,Flow Cytometry validation (1/100 dilution) in Bone marrow derived macrophages (Cat no:10298-1-AP)
FH

Charlotte (Verified Customer) (07-29-2022)

Cell fraction performed on NIH-3T3 cells to show the nucleus part. Blot super clean. Antibody specific. Easy to reveal.

  • Applications: Western Blot
  • Primary Antibody Dilution: 1/1000
  • Cell Tissue Type: NIH-3T3
Lamin A/C Antibody Western Blot validation (1/1000 dilution) in NIH-3T3 (Cat no:10298-1-AP)
FH

S (Verified Customer) (12-31-2021)

good antibody.

  • Applications: Western Blot
  • Primary Antibody Dilution: 1:2000
  • Cell Tissue Type: HEK293T
Lamin A/C Antibody Western Blot validation (1:2000 dilution) in HEK293T (Cat no:10298-1-AP)
FH

Azita (Verified Customer) (06-16-2021)

It was used as a marker in WB to confirm proper nuclear fractionation of cell lysate.

  • Applications: Western Blot
  • Primary Antibody Dilution: 1:1000
  • Cell Tissue Type: NSC-34 cell line
FH

Declan (Verified Customer) (11-29-2018)

  • Applications: Western Blot,
  • Primary Antibody Dilution: 1/5000
  • Cell Tissue Type: Human brain homogenate