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N8664

Anti-NONO (C-terminal) antibody produced in rabbit

~1.0 mg/mL, affinity isolated antibody, buffered aqueous solution

Synonym(e):

Anti-NMT55, Anti-NRB54, Anti-Non-pou domain-containing octamer-binding protein, Anti-Nuclear RNA-binding protein, 54-KD, Anti-p54nrb

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PackungsgrößeSKUVerfügbarkeitPreis
200 μL
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€ 557,00

Über diesen Artikel

NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
polyclonal
Application:
IF, IP, WB
Citations:
11

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biological source

rabbit

Quality Level

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

mol wt

antigen ~55 kDa

species reactivity

human

concentration

~1.0 mg/mL

technique(s)

immunoprecipitation (IP): 2.5-5 μg using HeLa cell lysates, indirect immunofluorescence: 2-5 μg/mL using paraformaldehyde fixed HeLa cells, western blot: 1-2 μg/mL using NIH-3T3 cell lysates

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... NONO(4841)

General description

Non-POU domain containing octamer binding (NONO) is ubiquitously expressed and comprises of two tandem RNP-type RNA- recognition motifs and a putative helix-turn-helix domain followed by a highly charged region. It is enriched in paraspeckles, a nucleoplasmic compartment and relocalizes to cap structures at the nucleolar periphery when transcription is inhibited.
Non-POU domain containing octamer binding protein (NONO) is part of the Drosophila behavior/human splicing (DBHS) protein family. It has a molecular weight of 54kDa and the gene encoding it is localized on human chromosome Xq13.1.

Application

Anti-NONO (C-terminal) antibody produced in rabbit has been used in immunoblotting and immunofluorescence.
Anti-NONO (N-terminal) antibody produced in rabbit has been used in immunoprecipitation.

Biochem/physiol Actions

NONO (also termed as p54nrb) is a nuclear protein implicated in numerous processes including transcription, pre-mRNA processing, nuclear retention of edited RNA and DNA relaxation. NONO was suspected to be involved in pre-mRNA splicing. Later it was found that NONO and PSF mediate different functions depending on their intracellular location.
Non-POU domain containing octamer binding protein (NONO) modulates transcription. Loss-of-function of the protein has been linked to human intellectual disability. The protein also has a role in synaptic transcription and regulation of the circadian clock. NONO also has a function in DNA damage response.

Physical form

Solution in 0.01 M phos­phate buffered saline, pH 7.4, containing 15 mM sodium azide.

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
SAB4200155Y0396HPA054094
antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

Quality Level

200

Quality Level

-

Quality Level

200

Quality Level

100

biological source

rabbit

biological source

rabbit

biological source

rabbit

biological source

rabbit

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

technique(s)

immunoprecipitation (IP): 2.5-5 μg using HeLa cell lysates, western blot: 1-2 μg/mL using NIH-3T3 cell lysates, indirect immunofluorescence: 2-5 μg/mL using paraformaldehyde fixed HeLa cells

technique(s)

immunoprecipitation (IP): 5.0-10 μg, indirect immunofluorescence: 1.25-2.5 μg/mL using fixed HEK-293T cells, western blot: 1-2 μg/mL using HeLa cell lysates

technique(s)

immunoprecipitation (IP): 5-10 μg using HEK-293T cell lysates, indirect immunofluorescence: 2-5 μg/mL using paraformaldehyde-fixed NIH-3T3 cells, western blot: 0.5-1 μg/mL using PC12 cell lysates

technique(s)

immunoblotting: 0.04-0.4 μg/mL, immunofluorescence: 0.25-2 μg/mL, immunohistochemistry: 1:1000-1:2500

clone

polyclonal

clone

polyclonal

clone

polyclonal

clone

polyclonal


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Lagerklasse

10 - Combustible liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable



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Verwandter Inhalt


Prefrontal cortex shotgun proteome analysis reveals
altered calcium homeostasis and immune system
imbalance in schizophrenia
Daniel Martins-de-Souza
European Journal of Anaesthesiology. Supplement (2009)
Promoter-Dependent Translation Controlled by p54nrb and hnRNPM during Myoblast Differentiation
Nader A
PLoS ONE (2015)
A crystallographic study of human NONO (p54nrb): overcoming pathological problems with purification, data collection and noncrystallographic symmetry
Knott GJ, et al.
Acta crystallographica. Section D, Structural biology, 761-761 (2016)



Global Trade Item Number

SKUGTIN
N8664-200UL04061838032089

Questions

  1. Can I get information about the epitope (exact C-terminal region) that was used to generate this antibody? Thanks

    1 answer
    1. The immunogen is a synthetic peptide corresponding to a sequence at the C-terminal of human NONO (GeneID: 4841) conjugated to KLH. The exact immunogen sequence is proprietary.

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