Anti-beta Catenin (phospho S552) antibody [EPR28411-7]
- 20ul selling size
- RabMAb
- Recombinant
- KO Validated
- Lab Essentials
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Rabbit Recombinant Monoclonal beta Catenin phospho S552 antibody. Suitable for WB, Dot, IP and reacts with Human, Mouse, Synthetic peptide - Human samples.
View Alternative Names
CTNNB, OK/SW-cl.35, PRO2286, CTNNB1, Catenin beta-1, Beta-catenin
- IP
Supplier Data
Immunoprecipitation - Anti-beta Catenin (phospho S552) antibody [EPR28411-7] (AB314502)
beta Catenin (phospho S552) was immunoprecipitated from 0.35 mg SK-N-MC (human brain epithelial cell) treated with 100 μM forskolin for 30 minutes whole cell lysate with ab314502 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab314502 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : SK-N-MC (human brain epithelial cell) treated with 100 μM forskolin for 30 minutes whole cell lysate
Lane 2 : ab314502 IP in SK-N-MC (human brain epithelial cell) treated with 100 μM forskolin for 30 minutes whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab314502 in SK-N-MC treated with 100 μM forskolin for 30 minutes whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
All lanes:
Immunoprecipitation - Anti-beta Catenin (phospho S552) antibody [EPR28411-7] (ab314502) at 1/30 dilution
All lanes:
SK-N-MC (human brain epithelial cell) treated with 100 ?M forskolin for 30 minutes whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 145s
- WB
Supplier Data
Western blot - Anti-beta Catenin (phospho S552) antibody [EPR28411-7] (AB314502)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 30806153).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
In Western blot, Anti-Catenin beta-1 antibody - Total protein control (ab32572) staining at 1/1000 dilution.
All lanes:
Western blot - Anti-beta Catenin (phospho S552) antibody [EPR28411-7] (ab314502) at 1/1000 dilution
Lane 1:
Untreated SK-N-MC (human brain epithelial cell) whole cell lysate (untreated membrane) at 20 µg
Lane 2:
SK-N-MC treated with 100 uM forskolin for 30 minutes whole cell lysate (untreated membrane) at 20 µg
Lane 3:
SK-N-MC treated with 100 uM forskolin for 30 minutes whole cell lysate (Lambda phosphatase treated membrane) at 20 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 1/100000 dilution
Observed band size: 85 kDa,90 kDa,36 kDa
false
Exposure time: 15s
- WB
Supplier Data
Western blot - Anti-beta Catenin (phospho S552) antibody [EPR28411-7] (AB314502)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 30806153).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
In Western blot, Anti-Catenin beta-1 antibody - Total protein control (ab32572) staining at 1/1000 dilution.
All lanes:
Western blot - Anti-beta Catenin (phospho S552) antibody [EPR28411-7] (ab314502) at 1/1000 dilution
Lane 1:
SW480 (human colorectal adenocarcinoma epithelial cell) whole cell lysate (untreated membrane) at 20 µg
Lane 2:
SW480 whole cell lysate (Lambda phosphatase membrane) at 20 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 1/100000 dilution
Observed band size: 85 kDa,90 kDa,36 kDa
true
Exposure time: 136s
- WB
Supplier Data
Western blot - Anti-beta Catenin (phospho S552) antibody [EPR28411-7] (AB314502)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 30806153).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-beta Catenin (phospho S552) antibody [EPR28411-7] (ab314502) at 1/1000 dilution
All lanes:
Mouse brain tissue lysate at 20 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 1/100000 dilution
Observed band size: 85 kDa,90 kDa,36 kDa
false
Exposure time: 59s
- WB
Supplier Data
Western blot - Anti-beta Catenin (phospho S552) antibody [EPR28411-7] (AB314502)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 30806153).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
In Western blot, Anti-Catenin beta-1 antibody - Total protein control (ab32572) staining at 1/1000 dilution.
All lanes:
Western blot - Anti-beta Catenin (phospho S552) antibody [EPR28411-7] (ab314502) at 1/1000 dilution
Lane 1:
NIH/3T3 (mouse embryonic fibroblast) starved for 24 hours whole cell lysate (untreated membrane) at 20 µg
Lane 2:
NIH/3T3 starved for 24 hours, then treated with 100 uM forskolin for 20 minutes whole cell lysate (untreated membrane) at 20 µg
Lane 3:
NIH/3T3 starved for 24 hours, then treated with 100 uM forskolin for 20 minutes whole cell lysate (Lambda phosphatase treated membrane) at 20 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 1/100000 dilution
Observed band size: 85 kDa,90 kDa,36 kDa
false
Exposure time: 103s
- Dot
Supplier Data
Dot Blot - Anti-beta Catenin (phospho S552) antibody [EPR28411-7] (AB314502)
Dot blot analysis of beta Catenin (phospho S552) using ab314502 at 1 : 1000 (0.496 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution.
Exposure time : 180 seconds.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
This antibody does not cross-react with non-phospho gamma Catenin peptide covering aa 534-548.
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 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
This protein plays roles in both cell adhesion and the regulation of gene expression. Beta Catenin is a critical component of the Wnt signaling pathway where it can form complexes with other proteins to influence gene transcription. In the absence of Wnt signaling beta Catenin levels are low due to its degradation. However when the pathway is active it accumulates in the cytoplasm and eventually translocates to the nucleus where it interacts with TCF/LEF transcription factors to regulate the expression of target genes.
Pathways
Beta Catenin plays a central role in the Wnt signaling pathway and influences cell fate decisions and cellular proliferation. It acts in concert with proteins such as Dishevelled (DVL) and Axin to coordinate these important biological processes. In the absence of Wnt signaling proteins such as APC and GSK-3β are responsible for beta Catenin degradation keeping its cellular levels in check. Beta Catenin’s interaction with transcription factors in the nucleus makes it pivotal in the regulation of cell and tissue homeostasis.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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