Anti-Staufen/STAU1 antibody [EPR7966]
- 20ul selling size
- RabMAb
- Recombinant
- What is this?
5
(2 Reviews)
|
(2 Publications)
Rabbit Recombinant Monoclonal Staufen/STAU1 antibody. Suitable for WB, ICC/IF, Flow Cyt (Intra) and reacts with Rat, Human, Mouse samples. Cited in 2 publications.
View Alternative Names
STAU, STAU1, Double-stranded RNA-binding protein Staufen homolog 1
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-Staufen/STAU1 antibody [EPR7966] (AB137100)
Immunofluorescent analysis of HepG2 cells labelling Staufen/STAU1 with ab137100 at 1/250 dilution.
This image was generated using the unpurified version of the product.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-Staufen/STAU1 antibody [EPR7966] (AB137100)
Overlay histogram showing SHSY-5Y cells stained with ab137100 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Tween for 20 min. 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 (ab137100, 1/10000 dilution) for 30 min at 22°C. The secondary antibody used was Alexa Fluor® 488 goat anti-rabbit IgG (H&L) (ab150077) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (0.1μg/1x106 cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter. This antibody gave a positive signal in SHSY-5Y cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.
This image was generated using the unpurified version of the product.
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-Staufen/STAU1 antibody [EPR7966] (AB137100)
Immunofluorescent analysis of HeLa cells labelling Staufen/STAU1 with ab137100 at 1/250 dilution.
This image was generated using the unpurified version of the product.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-Staufen/STAU1 antibody [EPR7966] (AB137100)
Intracellular Flow Cytometry analysis of SH-SY5Y (Human neuroblastoma epithelial cell) cells labeling Staufen/STAU1 with Purified ab137100 at 1/50 dilution (10μg/ml) (red). Cells were fixed with 4% Paraformaldehyde. A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) secondary antibody was used at 1/2000. Isotype control - Rabbit monoclonal IgG (Black). Unlabeled control - Cell without incubation with primary antibody and secondary antibody (Blue).
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-Staufen/STAU1 antibody [EPR7966] (AB137100)
Immunocytochemistry/ Immunofluorescence analysis of Jurkat (Human T cell leukemia T lymphocyte) cells labeling Staufen/STAU1 with Purified ab137100 at 1 : 100 dilution (5.1 μg/ml). Cells were fixed in 4% Paraformaldehyde and permeabilized with 0.1% tritonX-100. Cells were counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) 1 : 200 (2.5 μg/ml). Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) was used as the secondary antibody at 1 : 1000 (2 μg/ml) dilution. DAPI nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.
- WB
Unknown
Western blot - Anti-Staufen/STAU1 antibody [EPR7966] (AB137100)
This image was generated using the unpurified version of the product.
All lanes:
Western blot - Anti-Staufen/STAU1 antibody [EPR7966] (ab137100) at 1/1000 dilution
Lane 1:
Jurkat cell lysate at 10 µg
Lane 2:
K562 cell lysate at 10 µg
Lane 3:
HepG2 cell lysate at 10 µg
Secondary
All lanes:
Goat anti-rabbit HRP at 1/2000 dilution
Predicted band size: 63 kDa
Observed band size: 55 kDa
false
- WB
Lab
Western blot - Anti-Staufen/STAU1 antibody [EPR7966] (AB137100)
All lanes:
Western blot - Anti-Staufen/STAU1 antibody [EPR7966] (ab137100) at 1/1000 dilution
Lane 1:
HepG2 (Human hepatocellular carcinoma epithelial cell) whole cell lysates at 20 µg
Lane 2:
HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysates at 20 µg
Lane 3:
Mouse brain lysates at 20 µg
Lane 4:
NIH/3T3 (Mouse embryonic fibroblast) whole cell lysates at 20 µg
Lane 5:
Neuro-2a (Mouse neuroblastoma neuroblast) whole cell lysates at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Predicted band size: 63 kDa
Observed band size: 55 kDa,63 kDa
false
- WB
Lab
Western blot - Anti-Staufen/STAU1 antibody [EPR7966] (AB137100)
All lanes:
Western blot - Anti-Staufen/STAU1 antibody [EPR7966] (ab137100) at 1/1000 dilution
All lanes:
Rat heart lysates at 15 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 63 kDa
Observed band size: 55 kDa,63 kDa
false
Related conjugates and formulations (1)
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Anti-Staufen/STAU1 antibody [EPR7966] - BSA and Azide free
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
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 (2)
Recent publications for all applications. Explore the full list and refine your search
Nucleic acids research 52:12021-12038 PubMed39217468
2024
Applications
Unspecified application
Species
Unspecified reactive species
Molecular & cellular proteomics : MCP 15:506-22 PubMed26598648
2015
Applications
ICC/IF
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