Apoptosis Western Blot Cocktail (pro/p17-caspase-3,cleaved PARP1,muscle actin) (ab136812)
概述
-
产品名称
Apoptosis Western Blot Cocktail (pro/p17-caspase-3,cleaved PARP1,muscle actin) -
种属反应性
与反应: Human
不与反应: Mouse, Rat -
产品概述
Cocktail of primary antibodies to detect apoptosis biomarkers caspase 3 and PARP, along with loading control muscle actin (42 kDa). The caspase 3 antibody (rabbit monoclonal) detects both the 32 kDa pro-caspase 3 as well as the p17 subunit of active caspase 3 generated by cleavage of the pro-caspase 3 at Asp175. The PARP antibody (mouse monoclonal) detects only the apoptosis-specific 89 kDa PARP fragment (cleaved-PARP) generated from the full length PARP by active caspases. Since the primary antibodies used are both mouse and rabbit, a secondary antibodies cocktail of GAM-HRP and GAR-HRP is provided.
-
说明
The Apoptosis western blot cocktail (ab136812) is designed to study the induction of apoptosis in response to various stimuli. The two main components of this cocktail are monoclonal antibodies specific to caspase 3 and PARP. Caspase 3 is one of the executioner caspases activated by proteolytic cleavage during apoptosis. The rabbit caspase 3 antibody of this cocktail detects both the 32 kDa pro-caspase 3 as well as the p17 subunit of the active caspase 3 generated by cleavage of the pro-caspase 3 at Asp175. Thus the induction of apoptosis can be followed by a decrease of the pro-caspase 3 or by an increase of the p17 caspase 3. Monitoring the changes in the pro-caspase 3 is particularly advantageous, since the proportion of caspase activation can be determined from the reduction of the pro-form from analysis of control and stimulated samples. Poly [ADP-ribose] polymerase 1 (PARP) is a DNA repair enzyme that is cleaved during apoptosis by activated caspases. The mouse PARP antibody of this cocktail detects only the apoptosis-specific 89 kDa PARP fragment (cleaved-PARP). This antibody does not react with the full-length PARP. Combined, these two antibodies provide biomarkers of apoptosis. The rabbit muscle actin antibody is provided as a loading control for sample to sample normalization. Since the primary antibodies are both mouse and rabbit, the cocktail of HRP-conjugated goat anti-rabbit and anti-mouse secondary antibodies is provided for convenience. The targets are easily resolved by Western blot given their different molecular weights.
-
经测试应用
适用于: WBmore details
性能
-
存放说明
Store at +4°C. Please refer to protocols. -
组件 200 µl 100X HRP Conjugated Secondary Antibody Cocktail 1 x 500µl 250X Primary Antibody Cocktail 1 x 200µl -
研究领域
-
别名
- ACTA1
- Actin, alpha skeletal muscle
- ADP-ribosyltransferase diphtheria toxin-like 1
see all -
数据库链接
- Entrez Gene: 58 Human
- Entrez Gene: 142 Human
- Entrez Gene: 836 Human
- Omim: 173870 Human
- Omim: 102610 Human
- Omim: 600636 Human
- SwissProt: P42574 Human
- SwissProt: P09874 Human
see all
相关产品
-
Related Products
应用
The Abpromise guarantee
Abpromise™承诺保证使用ab136812于以下的经测试应用
“应用说明”部分 下显示的仅为推荐的起始稀释度;实际最佳的稀释度/浓度应由使用者检定。
应用 | Ab评论 | 说明 |
---|---|---|
WB |
Use at an assay dependent concentration.
1/250 dilution for primary antibodies 1/100 dilution for secondary antibodies Suggested dilution buffer: 5% milk/PBS+0.05% Tween 20 |
说明 |
---|
WB
Use at an assay dependent concentration. 1/250 dilution for primary antibodies 1/100 dilution for secondary antibodies Suggested dilution buffer: 5% milk/PBS+0.05% Tween 20 |
图片
-
Lane 1: Jurkat cells, untreated
Lane 2: Jurkat cells treated with anti-FAS for 2 hours
Lane 3: Jurkat cells treated with anti-FAS for 4 hours
Lane 4: Jurkat cells treated with anti-FAS for 6 hours
All lysates at 20 µg/lane
Primary antibodies
All lanes: 250X Primary Antibodies Cocktail, 1/250 dilution.
Secondary antibodies
All lanes: 100X HRP-Conjugated Secondary Antibodies Cocktail (ab136812), 1/100 dilution. -
Lanes 1, 3, 5, 7: (ab136806) HeLa, vehicle treated
Lanes 2, 4, 6, 8: (ab136806) HeLa, 1 µM staurosporine (ab120056), 4 hours
All lysates at 20 µg per lane.
Primary antibodies
Lanes 1, 2: Cleaved PARP
Lanes 3, 4: Actin
Lanes 5, 6: Caspase 3
Lanes 7, 8: ab136812 250X Primary Antibodies Cocktail, 1/250 dilution
Secondary antibodies
All lanes: ab136812 100X HRP-Conjugated Secondary Antibodies Cocktail, 1/100 dilution.
实验方案
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
数据表及文件
-
SDS download
-
Datasheet download
文献 (30)
ab136812 被引用在 30 文献中.
- Bortot B et al. Advanced photodynamic therapy with an engineered M13 phage targeting EGFR: Mitochondrial localization and autophagy induction in ovarian cancer cell lines. Free Radic Biol Med 179:242-251 (2022). PubMed: 34808331
- Lee A et al. Synergism of a novel MCL‑1 downregulator, acriflavine, with navitoclax (ABT‑263) in triple‑negative breast cancer, lung adenocarcinoma and glioblastoma multiforme. Int J Oncol 60:N/A (2022). PubMed: 34913076
- Friedman B et al. Adenosine A2A receptor signaling promotes FoxO associated autophagy in chondrocytes. Sci Rep 11:968 (2021). PubMed: 33441836
- Park HS et al. Human BM-MSC secretome enhances human granulosa cell proliferation and steroidogenesis and restores ovarian function in primary ovarian insufficiency mouse model. Sci Rep 11:4525 (2021). PubMed: 33633319
- Yamakawa H et al. Growth Inhibitory Effects of Ester Derivatives of Menahydroquinone-4, the Reduced Form of Vitamin K2(20), on All-Trans Retinoic Acid-Resistant HL60 Cell Line. Pharmaceutics 13:N/A (2021). PubMed: 34065416