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Lamin A/C Polyklonaler Antikörper

Lamin A/C Polyklonal Antikörper für FC, IF, IHC, IP, WB, ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human, Maus, Ratte und mehr (2)

Anwendung

WB, IP, IHC, IF, FC, ELISA

Konjugation

Unkonjugiert

Kat-Nr. : 10298-1-AP

Synonyme

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

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Geprüfte Anwendungen

Erfolgreiche Detektion in WBA431-Zellen, A375-Zellen, C6-Zellen, HEK-293-Zellen, HeLa-Zellen, HUVEC-Zellen, Maus-Eierstockgewebe, NIH/3T3-Zellen, SKOV-3-Zellen
Erfolgreiche IPHeLa-Zellen, A375-Zellen
Erfolgreiche Detektion in IHCMausherzgewebe
Hinweis: Antigendemaskierung mit TE-Puffer pH 9,0 empfohlen. (*) Wahlweise kann die Antigendemaskierung auch mit Citratpuffer pH 6,0 erfolgen.
Erfolgreiche Detektion in IFHepG2-Zellen, HeLa-Zellen
Erfolgreiche Detektion in FCHEK-293T-Zellen

Empfohlene Verdünnung

AnwendungVerdünnung
Western Blot (WB)WB : 1:5000-1:50000
Immunpräzipitation (IP)IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
Immunhistochemie (IHC)IHC : 1:2000-1:8000
Immunfluoreszenz (IF)IF : 1:400-1:1600
Durchflusszytometrie (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

Produktinformation

10298-1-AP bindet in WB, IP, IHC, IF, FC, ELISA Lamin A/C und zeigt Reaktivität mit human, Maus, Ratten

Getestete Reaktivität human, Maus, Ratte
In Publikationen genannte Reaktivitäthuman, Affe, Ente, Maus, Ratte
Wirt / Isotyp Kaninchen / IgG
Klonalität Polyklonal
Typ Antikörper
Immunogen Lamin A/C fusion protein Ag0408
Vollständiger Name lamin A/C
Berechnetes Molekulargewicht 65 kDa
Beobachtetes Molekulargewicht 65 kDa, 70 kDa
GenBank-ZugangsnummerBC003162
Gene symbol LMNA
Gene ID (NCBI) 4000
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Antigen-Affinitätsreinigung
Lagerungspuffer PBS mit 0.02% Natriumazid und 50% Glycerin pH 7.3.
LagerungsbedingungenBei -20°C lagern. Nach dem Versand ein Jahr lang stabil Aliquotieren ist bei -20oC Lagerung nicht notwendig. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

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.

Protokolle

Produktspezifische Protokolle
WB protocol for Lamin A/C antibody 10298-1-APProtokoll herunterladen
IHC protocol for Lamin A/C antibody 10298-1-APProtokoll herunterladen
IF protocol for Lamin A/C antibody 10298-1-APProtokoll herunterladen
IP protocol for Lamin A/C antibody 10298-1-APProtokoll herunterladen
Standard-Protokolle
Klicken Sie hier, um unsere Standardprotokolle anzuzeigen

Publikationen

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

Rezensionen

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