Rabbit Polyclonal Staufen/STAU1 antibody. Suitable for IP, WB, IHC-P, ICC/IF and reacts with Human samples. Cited in 25 publications.
View Alternative Names
STAU, STAU1, Double-stranded RNA-binding protein Staufen homolog 1
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-Staufen/STAU1 antibody (AB73478)
ICC/IF image of ab73478 stained HeLa cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab73478, 5µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM. This antibody also gave a positive result in 100% methanol fixed (5 min) MCF7 cells at 5µg/ml.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Staufen/STAU1 antibody (AB73478)
IHC image of Staufen/STAU1 staining in Human Cervical Cancer FFPE section, performed on a BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab73478, 5μg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX
- IP
Unknown
Immunoprecipitation - Anti-Staufen/STAU1 antibody (AB73478)
Staufen/STAU1 was immunoprecipitated using 0.5mg SW480 whole cell extract, 5μg of Rabbit polyclonal to Staufen/STAU1 and 50μl of protein G magnetic beads (+). No antibody was added to the control (-).
The antibody was incubated under agitation with Protein G beads for 10min, SW480 whole cell extract lysate diluted in RIPA buffer was added to each sample and incubated for a further 10min under agitation.
Proteins were eluted by addition of 40μl SDS loading buffer and incubated for 10min at 70oC; 10μl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab73478.
Secondary : Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697)..
Band : 63kDa : Staufen/STAU1; non specific - 75kDa : We are unsure as to the identity of this extra band.
All lanes:
Immunoprecipitation - Anti-Staufen/STAU1 antibody (ab73478)
Predicted band size: 63 kDa
false
- WB
Project
Western blot - Anti-Staufen/STAU1 antibody (AB73478)
All lanes:
Western blot - Anti-Staufen/STAU1 antibody (ab73478) at 1 µg/mL
Lane 1:
SK N BE (Human neuroblastoma) Whole Cell Lysate at 10 µg
Lane 2:
SW480 (Human colon adenocarcinoma cell line) Whole Cell Lysate at 10 µg
Secondary
All lanes:
Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution
Predicted band size: 63 kDa
Observed band size: 63 kDa,95 kDa
true
Exposure time: 3min
Reactivity data
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Staufen1 participates in mRNA transport and localization within cells especially neurons. It forms part of a ribonucleoprotein complex which is involved in the movement of mRNA to distinct subcellular sites facilitating localized protein synthesis. This function is critical for the development and maintenance of cellular structures especially in cells with polarized functions such as neurons where precise protein localization is necessary for synaptic function and plasticity.
Pathways
Staufen1 is essential in processes related to mRNA decay and translation regulation. It is actively involved in the nonsense-mediated mRNA decay pathway ensuring the quality control of mRNA transcripts and preventing the synthesis of defective proteins. Additionally STAU1 interacts with proteins such as UPF1 an important player in this mRNA surveillance mechanism highlighting its role in ensuring accurate protein translation and cellular health.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Publications (25)
Recent publications for all applications. Explore the full list and refine your search
Cell death & disease 15:599 PubMed39155279
2024
Applications
Unspecified application
Species
Unspecified reactive species
Genes & development 38:294-307 PubMed38688681
2024
Applications
Unspecified application
Species
Unspecified reactive species
Molecular and cellular biology 44:43-56 PubMed38347726
2024
Applications
Unspecified application
Species
Unspecified reactive species
Science advances 8:eabo5578 PubMed36170367
2022
Applications
Unspecified application
Species
Unspecified reactive species
International journal of molecular sciences 23: PubMed35008641
2021
Applications
Unspecified application
Species
Unspecified reactive species
Adipocyte 10:350-360 PubMed34224297
2021
Applications
Unspecified application
Species
Unspecified reactive species
BMC cancer 21:120 PubMed33541283
2021
Applications
Unspecified application
Species
Unspecified reactive species
Frontiers in aging neuroscience 12:578719 PubMed33024434
2020
Applications
Unspecified application
Species
Unspecified reactive species
Journal of leukocyte biology 109:593-603 PubMed32829531
2020
Applications
Unspecified application
Species
Unspecified reactive species
Neurochemistry international 139:104808 PubMed32711020
2020
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com