Anti-p53 抗体 [PAb 240]
Anti-p53 antibody [PAb 240]
- KO Validated
- Lab Essentials
- 了解详情
4
(56 Reviews)
|
(530 Publications)
Anti-p53 antibody [PAb 240] (ab26) is a mouse monoclonal antibody detecting p53 in Western Blot, IP, ICC/IF. Suitable for Human, Mouse.
- KO validated for confirmed specificity
- Over 400 publications
- Trusted since 1998
查看别名
P53, Trp53, Tp53, Cellular tumor antigen p53, Tumor suppressor p53
- WB
Supplier Data
Western blot - Anti-p53 antibody [PAb 240] (AB26)
Lanes 1-6 : Merged (red and green) signal.
ab26 was shown to specifically react with p53 in wild type HCT116 cells treated with irinotecan. No band was observed in p53 knockout HCT116 cells. Wild-type and p53 knockout samples, positive and negative controls were subjected to SDS-PAGE. ab26 and ab181602 (loading control to GAPDH) were diluted 5 μg/mL and 1/10,000 respectively and incubated overnight at 4°C. Blots were developed with goat anti-rabbit IgG (H + L) and goat anti-mouse IgG (H + L) secondary antibodies at 1/10,000 dilution for 1 h at room temperature before imaging.
Wild-type and p53 knockout HCT116 cell lysates were kindly provided by a collaborator.
All lanes:
Western blot - Anti-p53 antibody [PAb 240] (ab26) at 5 µg/mL
Lane 1:
Wild-type HCT116 cell lysate at 30 µg
Lane 2:
Wild-type HCT116 + irinotecan (10 µM, 24 hours) cell lysate at 30 µg
Lane 3:
p53 knockout HCT116 cell lysate at 30 µg
Lane 4:
p53 knockout HCT116 + irinotecan (10 µM, 24 hours) cell lysate at 30 µg
Lane 5:
A431 cell lysate (positive control) at 20 µg
Lane 6:
Saos-2 cell lysate (negative control) at 20 µg
Predicted band size: 43 kDa
Observed band size: 53 kDa
false
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-p53 antibody [PAb 240] (AB26)
ab26 stained in A431 cells. Cells were fixed with 4% paraformaldehyde (10min) at room temperature and incubated with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% triton for 1h at room temperature to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with ab26 at 1μg/ml and ab6046 (Rabbit polyclonal to beta tubulin) at 1ug/ml overnight at +4°C. The secondary antibodies were ab150177 (colored green) used at 1 ug/ml and ab150087 (pseudo-colored red) used at 2ug/ml for 1hour at room temperature. DAPI was used to stain the cell nuclei (colored blue) at a concentration of 1.43μM for 1hour at room temperature.
- IP
AbReview41852****
Immunoprecipitation - Anti-p53 antibody [PAb 240] (AB26)
p53 was immunoprecipitated from 7x106 HCT116 (human colon carcinoma cell line) cells with ab26 at 1/150 dilution. Western blot was performed from the immunoprecipitate using anti-p53 antibody. Donkey Anti-Mouse IgG H&L (Alexa Fluor® 750) preadsorbed (ab175739) was used as secondary antibody at 1/5000 dilution.
Lane 1 : HCT116 whole cell lysate 10 μg (Input).
Lane 2 : ab207799 IP in etoposide treated HCT116 whole cell lysate.
Lane 3 : ab207799 IP in etoposide treated HCT116 p53-/- whole cell lysate (negative control).
All lanes:
Anti p53 antibody
Secondary
All lanes:
Immunoprecipitation - Donkey Anti-Mouse IgG H&L (Alexa Fluor® 750) preadsorbed (<a href='/products/secondary-antibodies/donkey-mouse-igg-h-l-alexa-fluor-750-preadsorbed-ab175739'>ab175739</a>) at 1/5000 dilution
Predicted band size: 43 kDa
false
- WB
AbReview11453****
Western blot - Anti-p53 antibody [PAb 240] (AB26)
All lanes:
Western blot - Anti-p53 antibody [PAb 240] (ab26) at 1/2000 dilution
Lane 1:
Human breast cancer cell-line, MCF7 cells (p53 WT), whole cell lysate at 20 µg
Lane 2:
Human breast cancer cell-line, MDA231 cells (p53 Mutant), whole cell lysate at 20 µg
Secondary
All lanes:
HRP conjugated donkey anti-mouse antibody at 1/5000 dilution
Predicted band size: 43 kDa
Observed band size: 53 kDa,72 kDa
true
Exposure time: 10s
This image is courtesy of an Abreview submitted by Dr Cherie Blenkiron
- WB
Project10191****
Western blot - Anti-p53 antibody [PAb 240] (AB26)
All lanes:
Western blot - Anti-p53 antibody [PAb 240] (ab26) at 5 µg/mL
Lane 1:
HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 20 µg
Lane 2:
Hela Whole Cell Lysate - Bleomycin Treated (40U/ml) at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Mouse IgG H&L (HRP) preadsorbed (<a href='/products/secondary-antibodies/goat-mouse-igg-h-l-hrp-preadsorbed-ab97040'>ab97040</a>) at 1/5000 dilution
Predicted band size: 43 kDa
true
Exposure time: 4min
- WB
Lab
Western blot - Anti-p53 antibody [PAb 240] (AB26)
Lanes 1-2 : 1% BSA blocking buffer
Lanes 3-4 : 3% Milk blocking buffer
We recommend using 3% milk as the blocking agent for Western blot.
Lanes 1 - 2:
Western blot - Anti-p53 antibody [PAb 240] (ab26) at 1 µg/mL
Lanes 3 - 4:
Western blot - Anti-p53 antibody [PAb 240] (ab26) at 5 µg/mL
All lanes:
HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 20 µg
Secondary
All lanes:
Goat polyclonal to Mouse IgG - H&L - Pre-Adsorbed (HRP) at 1/5000 dilution
Predicted band size: 43 kDa
true
Exposure time: 4min
- WB
Lab
Western blot - Anti-p53 antibody [PAb 240] (AB26)
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 2% Bovine Serum Albumin before being incubated with ab26 overnight at 4°C. Antibody binding was detected using an anti-mouse HRP secondary antibody (ab97040), and visualised using ECL development solution ab133406.
All lanes:
Western blot - Anti-p53 antibody [PAb 240] (ab26) at 1 µg/mL
All lanes:
HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Mouse IgG H&L (HRP) preadsorbed (<a href='/products/secondary-antibodies/goat-mouse-igg-h-l-hrp-preadsorbed-ab97040'>ab97040</a>) at 1/50000 dilution
Predicted band size: 43 kDa
Observed band size: 53 kDa
true
Exposure time: 8min
- WB
Unknown
Western blot - Anti-p53 antibody [PAb 240] (AB26)
Primary : All Lanes : Anti-p53 antibody (ab26) at 5 μg/mL. Lane 1 : MW marker. Lane 2 : NIH/3T3 cells treated with vehicle for 24 hours. Lane 3 : NIH/3T3 cells treated with 1 μM doxorubicin for 24 hours Secondary : All Lanes : HRP-conjugated VeriBlot anti-Mouse IgG (ab131368) 1 : 1000. Lysates at 20 μg/lane. Performed under denaturing conditions. Developed using ECL technique. Blocking buffer : 5% milk in PBS.
All lanes:
Western blot - Anti-p53 antibody [PAb 240] (ab26)
Predicted band size: 43 kDa
false
反应性数据
产品详情
ab26 has been knockout validated in Western blot. The expected band was seen in wild type HCT116 cells treated with the DNA damaging agent irinotecan and no band was seen in TP53 knockout HCT116 cells.
Product Specifications
Anti-p53 antibody [PAb 240] (ab26) is a mouse monoclonal antibody and is validated for use in ICC/IF, IP, WB in human, mouse samples.
Anti-p53 antibody [PAb 240] (ab26) specifically detects p53 (UniProt ID: P04637; Molecular weight: 44kDa) and is sold in 100 µg selling sizes.
Quality and Validation
Abcam's high quality validation processes ensure Anti-p53 antibody [PAb 240] (ab26) has high sensitivity and specificity.
The specificity of Anti-p53 antibody [PAb 240] (ab26) has been confirmed by testing in knockout samples.
Anti-p53 antibody [PAb 240] (ab26) has been cited over 403 times in peer reviewed journals and is trusted by the scientific community.
Anti-p53 antibody [PAb 240] (ab26) has 54 independent reviews from customers.
Related Products
Conjugation-ready, carrier free format available for antibody clone PAb 240 - ab185238.
Want a custom formulation?
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com
性能和储存信息
形式
纯化工艺
存储溶液
运输条件
推荐的短期储存时间
推荐的短期储存条件
推荐的长期储存条件
分装信息
储存信息
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
P53 functions to control cell division and apoptosis serving as a guardian of the genome by preventing mutation accumulation. It does not form part of a larger complex under normal conditions but interacts with various other molecules to execute its functions. p53 can activate or suppress the transcription of numerous genes involved in cell cycle arrest DNA repair and programmed cell death allowing it to halt the progression of damaged cells and trigger repair mechanisms or eliminate those that cannot be repaired.
Pathways
P53 acts within several key biological pathways such as the p53 signaling pathway and the intrinsic apoptotic pathway. Its activity involves interaction with proteins like MDM2 which regulates p53 through ubiquitin-mediated degradation and ATM kinase which phosphorylates p53 in response to DNA damage. These interactions ensure appropriate cellular responses during stress and are vital for maintaining homeostasis.
产品实验方案
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靶点信息
文献 (530)
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