Anti-hnRNP U/p120 antibody [3G6]
4
(7 Reviews)
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(34 Publications)
Mouse Monoclonal hnRNP U/p120 antibody. Suitable for Flow Cyt, WB, IHC-P and reacts with Human samples. Cited in 34 publications. Immunogen corresponding to Native Full Length Protein corresponding to Human HNRNPU.
View Alternative Names
C1orf199, HNRPU, SAFA, U21.1, HNRNPU, Heterogeneous nuclear ribonucleoprotein U, hnRNP U, GRIP120, Nuclear p120 ribonucleoprotein, Scaffold-attachment factor A, p120, pp120, SAF-A
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-hnRNP U/p120 antibody [3G6] (AB10297)
ab10297 (4 μg/ml)) staining hnRNP U/p120 in human cerebellum using an automated system (DAKO Autostainer Plus). Using this protocol there is strong nuclear staining of Purkinje cells neurons.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 minutes. They were then blocked with a protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 minutes and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
- Flow Cyt
Unknown
Flow Cytometry - Anti-hnRNP U/p120 antibody [3G6] (AB10297)
Overlay histogram showing HeLa (human epithelial cell line from cervix adenocarcinoma) cells stained with ab10297 (red line). The cells were fixed with 100% methanol (5 minutes) and then permeabilized with 0.1% PBS-Tween for 20 minutes. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab10297, 1 μg/1x106 cells) for 30 minutes at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 minutes at 22°C. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2μg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HeLa cells fixed with 4% paraformaldehyde (10 minutes)/permeabilized in 0.1% PBS-Tween used under the same conditions.
- WB
Unknown
Western blot - Anti-hnRNP U/p120 antibody [3G6] (AB10297)
This correlates with the information published in the reference Dreyfuss, G. et. al.
All lanes:
Western blot - Anti-hnRNP U/p120 antibody [3G6] (ab10297) at 1/1000 dilution
Lane 1:
Cytoplasmic fraction of HeLa (human epithelial cell line from cervix adenocarcinoma) lysate
Lane 2:
Nuclear fraction of HeLa (human epithelial cell line from cervix adenocarcinoma) lysate
Predicted band size: 91 kDa
Observed band size: 120 kDa
false
- WB
AbReview7134****
Western blot - Anti-hnRNP U/p120 antibody [3G6] (AB10297)
All lanes:
Western blot - Anti-hnRNP U/p120 antibody [3G6] (ab10297) at 1/5000 dilution
All lanes:
HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen) whole cell lysate at 100 µg
Secondary
All lanes:
HRP conjugated sheep anti-mouse IgG
Predicted band size: 91 kDa
Observed band size: 120 kDa,60 kDa,80 kDa
true
Exposure time: 1min
This image is courtesy of an Abreview submitted by Dr Stoil Dmitrov
Reactivity data
Properties and storage information
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Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
HnRNP U plays a significant role in organizing chromatin architecture and facilitating transcription regulation. It often associates with other hnRNPs to form ribonucleoprotein complexes which are central in RNA metabolism. Importantly hnRNP U's capacity to interact with chromatin allows it to participate in chromatin remodeling which is necessary for processes such as embryonic development and cellular differentiation. It modifies the transcriptional landscape by influencing the accessibility of transcription factors to their DNA targets.
Pathways
HnRNP U integrates into pathways controlling gene expression and RNA processing. It is notably involved in pathways such as signal transduction and DNA damage response. This protein associates with the transcription machinery influencing the expression of genes responsive to cellular stress and proliferation signals. It interacts with proteins like p53 in the DNA damage response pathway which suggests a role in maintaining genomic stability by coordinating chromatin remodeling and transcription in response to stress.
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Target data
Publications (34)
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The American journal of pathology 194:13-29 PubMed37923250
2023
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JCI insight 8: PubMed36883566
2023
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Journal of cell science 135: PubMed34888666
2022
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Mammalian genome : official journal of the International Mammalian Genome Society 33:366-381 PubMed34859278
2021
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Molecular cell 81:3509-3525.e5 PubMed34320406
2021
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Molecular cell 81:2944-2959.e10 PubMed34166609
2021
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The Journal of cell biology 219: PubMed33053167
2020
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Cell 183:76-93.e22 PubMed32931733
2020
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Journal of extracellular vesicles 9:1786967 PubMed32944175
2020
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Journal of hematology & oncology 13:24 PubMed32216806
2020
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Product promise
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