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Merck
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Documenti fondamentali

05-714

Sigma-Aldrich

Anti-Lamin A/C Antibody, clone 14

clone 14, Upstate®, from mouse

Sinonimo/i:

Anti-CDCD1, Anti-CDDC, Anti-CMD1A, Anti-CMT2B1, Anti-EMD2, Anti-FPL, Anti-FPLD, Anti-FPLD2, Anti-HGPS, Anti-IDC, Anti-LDP1, Anti-LFP, Anti-LGMD1B, Anti-LMN1, Anti-LMNC, Anti-LMNL1, Anti-MADA, Anti-PRO1

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50 μG
CHF 501.00

CHF 501.00


Spedizione prevista il22 maggio 2025

Per il tuo target è disponibile un anticorpo ricombinante privo di conservanti. Prova ZRB1054

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Cambia visualizzazione
50 μG
CHF 501.00

About This Item

Codice UNSPSC:
12352203
eCl@ss:
32160702
NACRES:
NA.41

CHF 501.00


Spedizione prevista il22 maggio 2025

Per il tuo target è disponibile un anticorpo ricombinante privo di conservanti. Prova ZRB1054

Richiedi un ordine bulk

Origine biologica

mouse

Livello qualitativo

Forma dell’anticorpo

purified immunoglobulin

Tipo di anticorpo

primary antibodies

Clone

14, monoclonal

Reattività contro le specie

canine, chicken, human, rat, mouse

Produttore/marchio commerciale

Upstate®

tecniche

immunocytochemistry: suitable
western blot: suitable

Isotipo

IgG

N° accesso NCBI

N° accesso UniProt

Condizioni di spedizione

dry ice

modifica post-traduzionali bersaglio

unmodified

Informazioni sul gene

human ... LMNA(4000)

Descrizione generale

Nuclear lamins are composed of the type V intermediate filament proteins. Often referred to as nucleoskeletal proteins they play a key role in nuclear integrity, positioning of nuclear pores, and overall nuclear size and shape. They also play several key functional roles in the maintenance and propagation of the genome--replication, transcription-- as well as the disassembly and reassembly of the nucleus during cell division. In vitro studies have shown that dimers are the basic building blocks of higher order lamin structures and in low concentrations lamins are distributed throughout the nucleoplasm. In humans, there are two types of lamins: A-type lamins (lamins A and C), found primarily in differentiated cells, and B-type lamins (lamins B1 and B2), found in all nucleated cells. Nuclear lamins are involved in a number of essential nuclear functions, including nuclear envelope assembly and disassembly during cell division, DNA synthesis, transcription, and apoptosis. Nuclear lamins have been found to co-localize with DNA synthesis sites.

Specificità

Recognizes Lamin A, MW ~74 kDa and Lamin C, MW ~65 kDa.

Immunogeno

Peptide from human lamin A/C corresponding to amino acids 398 to 490.

Applicazioni

Anti-Lamin A/C Antibody, clone 14 detects level of Lamin A/C & has been published & validated for use in IC & WB.
Immunocytochemistry:
This antibody has been reported by an independent laboratory to detect Lamin A/C in human endothelial cells.
Research Category
Cell Structure
Research Sub Category
Cytoskeletal Signaling

Qualità

Evaluated by western blot on RIPA lysates from A431 cells.

Western Blot Analysis:
0.5-2 μg/mL of this antibody detected Lamin A/C in 20 μg of RIPA lysates from A431 cells.

Descrizione del bersaglio

~74/65 kDa

Linkage

Replaces: MABE481

Stato fisico

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG1 in buffer containing 50% storage buffer (20 mM sodium phosphate, pH 7.5, 0.15 M NaCl, 1 mg/mL BSA, 0.09% sodium azide) and 50% glycerol. Store at -20°C.

Stoccaggio e stabilità

Stable for 1 year at -20ºC from date of receipt.

Risultati analitici

Control
Positive Antigen Control: Catalog #12-301, non-stimulated A431 cell lysate. Add 2.5µL of 2-mercaptoethanol/100µL of lysate and boil for 5 minutes to reduce the preparation. Load 20µg of reduced lysate per lane for minigels.

Altre note

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Note legali

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

Esclusione di responsabilità

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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Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Jose D Debes et al.
Cancer research, 65(3), 708-712 (2005-02-12)
Alterations in nuclear structure distinguish cancer cells from noncancer cells. These nuclear alterations can be translated into quantifiable features by digital image analysis in a process known as quantitative nuclear morphometry. Recently, quantitative nuclear morphometry has been shown to predict
Sribalasubashini Muralimanoharan et al.
Endocrinology, 159(5), 2022-2033 (2018-03-17)
Dysregulation of human trophoblast invasion and differentiation with placental hypoxia can result in preeclampsia, a hypertensive disorder of pregnancy. Herein, we characterized the role and regulation of miR-1246, which is markedly induced during human syncytiotrophoblast differentiation. miR-1246 targets GSK3β and
Ubiquitin-dependent recruitment of the Bloom syndrome helicase upon replication stress is required to suppress homologous recombination.
Tikoo, S; Madhavan, V; Hussain, M; Miller, ES; Arora, P; Zlatanou, A; Modi, P; Townsend et al.
The Embo Journal null
T Sullivan et al.
The Journal of cell biology, 147(5), 913-920 (1999-12-01)
The nuclear lamina is a protein meshwork lining the nucleoplasmic face of the inner nuclear membrane and represents an important determinant of interphase nuclear architecture. Its major components are the A- and B-type lamins. Whereas B-type lamins are found in
Angelika Oehmig et al.
BMC genomics, 9, 441-441 (2008-09-26)
The identification of novel drug targets by assessing gene functions is most conveniently achieved by high-throughput loss-of-function RNA interference screening. There is a growing need to employ primary cells in such screenings, since they reflect the physiological situation more closely

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