Anti-NONO (N-terminal) antibody produced in rabbit
SIGMA/N8789 - ~1.0 mg/mL, affinity isolated antibody, buffered aqueous solution
Synonym: Anti-NMT55; Anti-NRB54; Anti-Non-pou domain-containing octamer-binding protein; Anti-p54nrb
Product Type: Chemical
Immunofluorescence Predominant Nuclear localization of NONO in HeLa cells. Cells were fixed and stained with 5 μg/mL Rabbit Anti-NONO (N-terminal) (Cat. No. N8789) followed by Goat Anti-Rabbit, Cye3 conjugate. The cells were counterstained with DAPI (blue) to stain nuclei. (x40 magnification).
Immunoprecipitation Rabbit Anti-NONO (N-terminal) (Cat. No. N8789) and Rabbit Anti-NONO (C-Terminal) (Cat. No. N8664) were used to immunoprecipitate human NONO from HeLa cell lysate. Detection antibody: Anti-NONO (C-terminal) (Cat. No. N8664). Lanes 1. IP antibody: 2.5 μg Anti-NONO (N-terminal) 2. IP antibody: 5 μg Anti-NONO (N-terminal) 3. IP antibody: 2.5 μg Anti-NONO (C-terminal) 4. IP antibody: 5 μg Anti-NONO (C-terminal) 5. Negative control: Anti-NONO (N-terminal) IP without cell lysate 6. Negative control: Anti-NONO (C-terminal) IP without cell lysate 7. Negative control: Anti-NONO (N-terminal) IB without IP antibody 8. Negative control: Anti-NONO (C-terminal) IB without IP antibody 9. Immunoblotting positive control: total HeLa cell lysate blot with Anti-NONO (N-terminal) 10. Immunoblotting positive control: total HeLa cell lysate blot with Anti-NONO (N-terminal)
Immunoblotting Lysates of various cell lines were separated on SDS-PAGE and probed with 2 μg/mL Rabbit Anti-NONO (N-terminal) (Cat. No. N8789). The antibody was developed with Goat Anti-Rabbit IgG (Cat. No. A0545) Peroxidase conjugate and a chemiluminescence substrate. Lanes 1. HEK-293T cells over expressing human NONO; 2. HeLa; 3. NIH-3T3; 4. A431
| antibody form | affinity isolated antibody |
| antibody product type | primary antibodies |
| biological source | rabbit |
| clone | polyclonal |
| concentration | ~1.0 mg/mL |
| conjugate | unconjugated |
| form | buffered aqueous solution |
| mol wt | antigen ~55 kDa |
| Quality Level | 200  |
| shipped in | dry ice |
| species reactivity | human |
| storage temp. | −20°C |
| target post-translational modification | unmodified |
| 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 lysate | |
| UniProt accession no. | Q15233  |
| Application: | Anti-NONO (N-terminal) antibody produced in rabbit has been used in immunoprecipitation, immunoblotting. It may be used for immunofluorescence. |
| Biochem/physiol Actions: | 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. |
| Biochem/physiol Actions: | Non-POU Domain-Containing Octamer-Binding Protein (NONO) is a nuclear protein implicated in numerous processes including transcription, pre-mRNA processing, nuclear retention of edited RNA, and DNA relaxation. NONO is phosphorylated on multiple sites during mitosis and is a target of the peptidylprolyl isomerase (Pin1). |
| 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. |
| General description: | 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. |
| General description: | Non-POU Domain-Containing Octamer-Binding Protein (NONO) is ubiquitously expressed and is composed 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. |
| Physical form: | Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide. |
| RIDADR | NONH for all modes of transport |
| WGK Germany | nwg |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Storage Temp. | −20°C |
| UNSPSC | 12352203 |