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MABD116

Anti-Dux4 Antibody, clone 9A12

clone 9A12, from mouse

Synonim(y):

double homeobox protein 4, Double homeobox protein 10, Double homeobox protein 4/10, Dux-4

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Gabaryty przesyłkiSKUDostępnośćCena netto
100 μL

Przewidywany termin wysyłki18 maja 2026zKuehne + Nagel Sp. z o.o.

1990,00 zł

Informacje o tej pozycji

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
9A12, monoclonal
Application:
EMSA, ICC, IP, WB
Citations:
6

1990,00 zł


Przewidywany termin wysyłki18 maja 2026Szczegóły


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biological source

mouse

Quality Level

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

9A12, monoclonal

species reactivity

human

technique(s)

electrophoretic mobility shift assay: suitable, immunocytochemistry: suitable, immunoprecipitation (IP): suitable, western blot: suitable

isotype

IgG1κ

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... DUX4(100288687)

General description

Dux4 is a homeodomain protein with a similar protein sequence to Pax3 and Pax7. Defects in Dux4 may be the cause of facioscapulohumeral muscular dystrophy (FSHD). FSHD is characterized by weakness of the muscles of the face, upper-arm and shoulder girdle. Ectopic expression of Dux4 in skeletal muscle activates the expression of stem cell and germline genes, and, when overexpressed in somatic cells, Dux4 can ultimately lead to cell death.
~58 kDa observed

Immunogen

Epitope: domain of: C-Terminal region
recombinant protein corresponding to the domain of: C-Terminal region of Human Dux4.

Application

Detect Dux4 using this mouse monoclonal antibody, Anti-Dux4 Antibody, clone 9A12 validated for use in western blotting, ICC, Electrophoretic Mobility Shift Assay & IP.
Research Category
Stem Cell Research

Stem Cell Research
Research Sub Category
Muscle Physiology

Developmental Signaling
This antibody has been shown to work in immunocytochemistry applications (Dixit et al. 2007). This antibody has been shown to work in electrophoretic mobility shift assays (Dixit et al. 2007). This antibody has been shown to work in immunoprecipitation applications (Anseau et al., 2009).

Physical form

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG1κ supernatant 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

Control
Human skeletal muscle tissue lysate.
Evaluated by Western Blot in a human skeletal muscle tissue lysate. Western Blot Analysis: A 1:250 dilution of this antibody detected Dux4 in a human skeletal muscle tissue lysate.

Other Notes

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

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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Ta pozycja
SAB5200019SAB4500659MABE331
Gene Information

human ... DUX4(100288687)

Gene Information

human ... DUX4(22947)

Gene Information

human ... DLX4(1748)

Gene Information

human ... MDM2(4193)
mouse ... Mdm2(17246)

clone

9A12, monoclonal

clone

P2B1, monoclonal

clone

polyclonal

clone

4B2C1.11, monoclonal

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

species reactivity

human

species reactivity

human

species reactivity

human

species reactivity

human, mouse

biological source

mouse

biological source

mouse

biological source

rabbit

biological source

mouse

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

affinity isolated antibody

antibody form

purified immunoglobulin


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Klasa składowania

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów



Thuy-Hang Nguyen et al.
International journal of molecular sciences, 25(6) (2024-03-28)
FacioScapuloHumeral muscular Dystrophy (FSHD) is one of the most prevalent inherited muscle disorders and is linked to the inappropriate expression of the DUX4 transcription factor in skeletal muscles. The deregulated molecular network causing FSHD muscle dysfunction and pathology is not
Eugénie Ansseau et al.
Genes, 8(3) (2017-03-10)
FacioScapuloHumeral muscular Dystrophy (FSHD) is one of the most prevalent hereditary myopathies and is generally characterized by progressive muscle atrophy affecting the face, scapular fixators; upper arms and distal lower legs. The FSHD locus maps to a macrosatellite D4Z4 repeat
Louise A Moyle et al.
eLife, 5 (2016-11-15)
Facioscapulohumeral muscular dystrophy (FSHD) involves sporadic expression of DUX4, which inhibits myogenesis and is pro-apoptotic. To identify target genes, we over-expressed DUX4 in myoblasts and found that the receptor tyrosine kinase Ret was significantly up-regulated, suggesting a role in FSHD.



Numer pozycji handlu globalnego

SKUNUMER GTIN
MABD11604053252931703

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