Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
- KO Validated
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Rabbit Recombinant Monoclonal beta Catenin antibody. Carrier free. Suitable for IHC-P, ICC/IF, IP, Dot, WB and reacts with Rat, Mouse, Human, Synthetic peptide - Human samples.
View Alternative Names
CTNNB, OK/SW-cl.35, PRO2286, CTNNB1, Catenin beta-1, Beta-catenin
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (AB278503)
This data was developed using ab246504, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human ovarian cancer tissue labelling beta Catenin non-phospho S37/T42 with ab246504 at 1/2000 dilution (0.2705 μg/ml) followed by a ready to use Leica DS9800 (Bond™ Polymer Refine Detection). Positive staining on human ovarian cancer. The section was incubated with ab246504 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Leica DS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (AB278503)
This data was developed using ab246504, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human colon tissue labelling beta Catenin non-phospho S37/T41 with ab246504 at 1/2000 dilution (0.2705 μg/ml) followed by a ready to use Leica DS9800 (Bond™ Polymer Refine Detection). Positive staining on human colon. The section was incubated with ab246504 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Leica DS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (AB278503)
This data was developed using ab246504, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded (A) Wild-type HAP1 (human chronic myelogenous leukemia near-haploid cell) cell pellet and (B) CTNNB1 KO HAP1 cell pellet labelling beta Catenin non-phospho S37/T45 with ab246504 at 1/2000 dilution (0.2705 μg/ml) followed by a ready to use Leica DS9800 (Bond® Polymer Refine Detection). Positive staining on (A) Wild-type HAP1 (human chronic myelogenous leukemia near-haploid cell) cell pellet. No staining on (B) CTNNB1 KO HAP1 cell pellet. The section was incubated with ab246504 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Leica DS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (AB278503)
This data was developed using ab246504 , the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized CTNNB1 KO HAP1 (CTNNB1 knockout human chronic myelogenous leukemia near-haploid cell line) cells labelling beta Catenin non-phospho S37/T44 with ab246504 at 1/100 (5.4 μg/ml) dilution, followed by ab150077 antibody at 1/1000 (2 μg/ml) dilution (Green). Confocal image showing membranous staining in parental HAP1 cell line, and staining in the CTNNB1 KO HAP1 cell line. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). ab195889 was used to counterstain tubulin at 1/200 (2.5 μg/ml) dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150077 at 1/1000 (2 μg/ml) dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (AB278503)
This data was developed using ab246504, the same antibody clone in a different buffer formulation.
beta Catenin (non-phospho S37/T41) was immunoprecipitated from 0.35 mg HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate 10 ug with ab246504 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab246504 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate 10 ug
Lane 2 : ab246504 IP in HeLa whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab246504 in HeLa whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 3 seconds
All lanes:
Immunoprecipitation - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] (<a href='/en-us/products/primary-antibodies/beta-catenin-non-phospho-s37-t41-antibody-epr23969-131-ab246504'>ab246504</a>)
Predicted band size: 85 kDa
Observed band size: 95 kDa
false
Exposure time: 3s
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (AB278503)
This data was developed using ab246504, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-101 permeabilized NIH/3T3 (mouse embryonic fibroblast) cells labelling beta Catenin non-phospho S37/T45 with ab246504 at 1/100 (5.4 μg/ml) dilution, followed by ab150077 antibody at 1/1000 (2 μg/ml) dilution (Green). Confocal image showing membranous and cytoplasmic staining in NIH/3T3 cell line. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). ab195889 was used to counterstain tubulin at 1/200 (2.5 μg/ml) dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150078 at 1/1000 (2 μg/ml) dilution.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (AB278503)
This data was developed using ab246504, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat colon tissue labelling beta Catenin non-phospho S37/T44 with ab246504 at 1/2000 dilution (0.2705 μg/ml) followed by a ready to use Leica DS9800 (Bond™ Polymer Refine Detection). Positive staining on rat colon. The section was incubated with ab246504 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Leica DS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (AB278503)
This data was developed using ab246504, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse colon tissue labelling beta Catenin non-phospho S37/T43 with ab246504 at 1/2000 dilution (0.2705 μg/ml) followed by a ready to use Leica DS9800 (Bond™ Polymer Refine Detection). Positive staining on mouse colon. The section was incubated with ab246504 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Leica DS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
- WB
Lab
Western blot - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (AB278503)
False colour image of Western blot : Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] staining at 1/1000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab246504 was shown to bind specifically to beta Catenin non-phospho(active) S37/T41. A band was observed at 90 kDa in wild-type HepG2 cell lysates with no signal observed at this size in CTNNB1 knockout cell line. To generate this image, wild-type and CTNNB1 knockout HepG2 cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 5 % milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) at 1/20000 dilution.
All lanes:
Western blot - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] (<a href='/en-us/products/primary-antibodies/beta-catenin-non-phospho-s37-t41-antibody-epr23969-131-ab246504'>ab246504</a>) at 1/1000 dilution
Lane 1:
Wild-type HepG2 cell lysate at 20 µg
Lane 2:
CTNNB1 knockout HepG2 cell lysate at 20 µg
Lane 2:
Western blot - Human CTNNB1 (beta Catenin) knockout Hep G2 cell line (<a href='/en-us/products/cell-lines/human-ctnnb1-beta-catenin-knockout-hep-g2-cell-line-ab277911'>ab277911</a>)
Lane 3:
HeLa cell lysate at 20 µg
Lane 4:
A431 cell lysate at 20 µg
Predicted band size: 85 kDa
Observed band size: 90 kDa
false
- WB
Lab
Western blot - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (AB278503)
This data was developed using ab246504, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Exposure time 92 seconds
An extra band around 45 kDa was observed.
All lanes:
Western blot - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] (<a href='/en-us/products/primary-antibodies/beta-catenin-non-phospho-s37-t41-antibody-epr23969-131-ab246504'>ab246504</a>) at 1/1000 dilution
Lane 1:
HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
HCT 116 (human colorectal carcinoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
LLC1 (mouse lung carcinoma ) whole cell lysate at 20 µg
Lane 4:
C6 (rat glial tumor glial cell) whole cell 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
Predicted band size: 85 kDa
Observed band size: 95 kDa
false
- WB
Lab
Western blot - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (AB278503)
This data was developed using ab246504, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : Intercept® (TBS) Blocking Buffer diluted with an equal volume of 0.1% TBST
The molecular weight observed is consistent with what has been described in the literature (PMID : 16288032).
Lanes 1-4 : Merged signal (red and green). Green - ab246504 observed at 92 kDa. Red - loading control ab8245 (Mouse monoclonal [6C5] to GAPDH) observed at 36 kDa.
Lanes 1-2 : ab246504 Anti-beta Catenin (non-phospho S37/T41) antibody [EPR23969-131] was shown to specifically react with beta Catenin in wild-type HeLa cells. Loss of signal was observed when knockout cell line ab255352 (knockout cell lysate ab263756) was used.
Lanes 3-4 : ab246504 Anti-beta Catenin (non-phospho S37/T41) antibody [EPR23969-131] was shown to specifically react with beta Catenin in wild-type HAP1 cells. Loss of signal was observed when knockout sample was used.
Wild-type and beta Catenin knockout samples were subjected to SDS-PAGE. ab246504 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated overnight at 4°C at 1 in 1000 dilution and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (ab216776) secondary antibodies at 1 in 10000 dilution for 1 hour at room temperature before imaging.
An extra band around 45 kDa was observed.
All lanes:
Western blot - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (ab278503) at 1/1000 dilution
Lane 1:
Wild-type HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
CTNNB1 (beta Catenin) knockout HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
Wild-type HAP1 (human chronic myelogenous leukemia near-haploid cell) whole cell lysate at 20 µg
Lane 4:
CTNNB1 (beta Catenin) knockout HAP1 (human chronic myelogenous leukemia near-haploid cell) whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG H&L (IRDye® 800CW) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-800cw-preadsorbed-ab216773'>ab216773</a>) and Goat Anti-Mouse IgG H&L (IRDye® 680RD) (<a href='/en-us/products/secondary-antibodies/goat-mouse-igg-h-l-irdye-680rd-preadsorbed-ab216776'>ab216776</a>) at 1/10000 dilution
Predicted band size: 85 kDa
Observed band size: 95 kDa
false
- WB
Lab
Western blot - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (AB278503)
This data was developed using ab246504, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
An extra band around 45 kDa was observed.
Exposure time : 3 minutes
All lanes:
Western blot - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] (<a href='/en-us/products/primary-antibodies/beta-catenin-non-phospho-s37-t41-antibody-epr23969-131-ab246504'>ab246504</a>) at 1/1000 dilution
Lane 1:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 2:
PC-12 (rat adrenal gland pheochromocytoma ) whole cell 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
Predicted band size: 85 kDa
Observed band size: 95 kDa
false
Exposure time: 3min
- Dot
Supplier Data
Dot Blot - Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131] - BSA and Azide free (AB278503)
This data was developed using ab246504, the same antibody clone in a different buffer formulation.
Dot blot analysis of beta Catenin (non-phospho S37/T41) using ab246504 at 1 : 1000 (0.541 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution.
Lane 1 : beta Catenin non-phospho-Ser33/Ser37/Thr41 peptide (aa 29-44)
Lane 2 : beta Catenin non-phospho-Ser33/Ser37/Thr41 peptide (aa 31-47)
Lane 3 : beta Catenin phospho-Ser33 non-phospho-Ser37/Thr41 peptide (aa 29-44)
Lane 4 : beta Catenin phospho-Ser37 non-phospho-Ser33/Thr41peptide (aa 29-44)
Lane 5 : beta Catenin phospho-Thr41 non-phospho-Ser33/Ser37 peptide (aa 29-47)
Lane 6 : beta Catenin phospho-Ser33/Ser37 non-phospho-Thr41 peptide (aa 29-47)
Lane 7 : beta Catenin phospho-Ser33/Thr41 non-phospho-Ser37 peptide (aa 29-47)
Lane 8 : beta Catenin phospho-Ser37/Thr41non-phospho-Ser33 peptide (aa 29-47)
Lane 9 : beta Catenin phospho-Ser33/Ser37/Thr41peptide (aa 29-47)
Exposure time : 81 seconds
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Related conjugates and formulations (8)
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Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131]
-
617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131]
-
519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131]
-
660 APC
APC Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131]
-
665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131]
-
578 PE
PE Anti-beta Catenin non-phospho S37/T41 antibody [EPR23969-131]
-
775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-beta Catenin non-phospho(active) S37/T41 antibody [EPR23969-131]
Reactivity data
Product details
ab278503 is the carrier-free version of ab246504.
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.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Beta-catenin non-phospho S37/T41 affects cellular behavior by modulating gene expression. It acts as a core component of the Wnt signaling pathway particularly in the regulation of gene transcription. In this pathway beta-catenin associates with transcription factors such as TCF/LEF to regulate target gene expression involved in processes like cell proliferation and differentiation. Unphosphorylated beta-catenin binds with protein complexes that regulate adhesion to ensure proper communication between cells.
Pathways
Beta-catenin non-phospho S37/T41 plays a pivotal role in the Wnt pathway a critical regulator of cell fate decisions. Within this context beta-catenin's stabilization and nuclear activity are vital for the pathway's transcriptional output. It works closely with proteins like APC (adenomatous polyposis coli) and Axin which act as regulators of its phosphorylation. Additionally beta-catenin interacts with E-cadherin at the cell membrane within the adherens junctions contributing to cell-cell adhesion processes.
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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