Alexa Fluor® 488荧光Anti-Cleaved PARP1抗体[4B5BD2] (ab170171)
Key features and details
- Alexa Fluor® 488 Mouse monoclonal [4B5BD2] to Cleaved PARP1
- Suitable for: ICC, Flow Cyt (Intra)
- Reacts with: Human
- Conjugation: Alexa Fluor® 488. Ex: 495nm, Em: 519nm
- Isotype: IgG1
Related conjugates and formulations
概述
-
产品名称
Alexa Fluor® 488荧光Anti-Cleaved PARP1抗体[4B5BD2]
参阅全部 Cleaved PARP1 一抗 -
描述
Alexa Fluor® 488荧光小鼠单克隆抗体[4B5BD2] to Cleaved PARP1 -
宿主
Mouse -
偶联物
Alexa Fluor® 488. Ex: 495nm, Em: 519nm -
经测试应用
适用于: ICC, Flow Cyt (Intra)more details -
种属反应性
与反应: Human
预测可用于: Chinese hamster不与反应: Mouse, Rat, Cow -
免疫原
Synthetic peptide within Human Cleaved PARP1 aa 200-300 (N terminal). The exact sequence is proprietary.
Database link: P09874 -
阳性对照
- HeLa cells treated with 1 µM staurosporine for 4 hours.
-
常规说明
Alexa Fluor® is a registered trademark of Molecular Probes, Inc, a Thermo Fisher Scientific Company. The Alexa Fluor® dye included in this product is provided under an intellectual property license from Life Technologies Corporation. As this product contains the Alexa Fluor® dye, the purchase of this product conveys to the buyer the non-transferable right to use the purchased product and components of the product only in research conducted by the buyer (whether the buyer is an academic or for-profit entity). As this product contains the Alexa Fluor® dye the sale of this product is expressly conditioned on the buyer not using the product or its components, or any materials made using the product or its components, in any activity to generate revenue, which may include, but is not limited to use of the product or its components: in manufacturing; (ii) to provide a service, information, or data in return for payment (iii) for therapeutic, diagnostic or prophylactic purposes; or (iv) for resale, regardless of whether they are sold for use in research. For information on purchasing a license to this product for purposes other than research, contact Life Technologies Corporation, 5781 Van Allen Way, Carlsbad, CA 92008 USA or outlicensing@thermofisher.com.
The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.
If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As
Product was previously marketed under the MitoSciences sub-brand.
性能
-
形式
Liquid -
存放说明
Shipped at 4°C. Store at +4°C. Avoid freeze / thaw cycle. Stable for 12 months at -20°C. Store In the Dark. -
存储溶液
Preservative: 0.02% Sodium azide
Constituents: 30% Glycerol (glycerin, glycerine), 1% BSA, 68% PBS -
Concentration information loading...
-
纯度
Ammonium Sulphate Precipitation -
克隆
单克隆 -
克隆编号
4B5BD2 -
同种型
IgG1 -
研究领域
相关产品
-
Alternative Versions
-
Isotype control
-
Related Products
应用
The Abpromise guarantee
Abpromise™承诺保证使用ab170171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 |
---|---|---|
ICC |
Use a concentration of 1 µg/ml.
Use Antigen Retrieval Buffer (100 mM Tris, 5% urea, pH 9.5) at 95°C for 10 min to boost signal. |
|
Flow Cyt (Intra) |
Use a concentration of 1 µg/ml.
ab171463 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody. |
说明 |
---|
ICC
Use a concentration of 1 µg/ml. Use Antigen Retrieval Buffer (100 mM Tris, 5% urea, pH 9.5) at 95°C for 10 min to boost signal. |
Flow Cyt (Intra)
Use a concentration of 1 µg/ml. ab171463 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody. |
靶标
-
功能
Involved in the base excision repair (BER) pathway, by catalyzing the poly(ADP-ribosyl)ation of a limited number of acceptor proteins involved in chromatin architecture and in DNA metabolism. This modification follows DNA damages and appears as an obligatory step in a detection/signaling pathway leading to the reparation of DNA strand breaks. Mediates the poly(ADP-ribosyl)ation of APLF and CHFR. Positively regulates the transcription of MTUS1 and negatively regulates the transcription of MTUS2/TIP150. With EEF1A1 and TXK, forms a complex that acts as a T-helper 1 (Th1) cell-specific transcription factor and binds the promoter of IFN-gamma to directly regulate its transcription, and is thus involved importantly in Th1 cytokine production. Required for PARP9 and DTX3L recruitment to DNA damage sites. PARP1-dependent PARP9-DTX3L-mediated ubiquitination promotes the rapid and specific recruitment of 53BP1/TP53BP1, UIMC1/RAP80, and BRCA1 to DNA damage sites. -
序列相似性
Contains 1 BRCT domain.
Contains 1 PARP alpha-helical domain.
Contains 1 PARP catalytic domain.
Contains 2 PARP-type zinc fingers. -
翻译后修饰
Phosphorylated by PRKDC and TXK.
Poly-ADP-ribosylated by PARP2. Poly-ADP-ribosylation mediates the recruitment of CHD1L to DNA damage sites.
S-nitrosylated, leading to inhibit transcription regulation activity. -
细胞定位
Nucleus. Nucleus, nucleolus. Localizes at sites of DNA damage. - Information by UniProt
-
数据库链接
- Entrez Gene: 100689463 Chinese hamster
- Entrez Gene: 142 Human
- Omim: 173870 Human
- SwissProt: Q9R152 Chinese hamster
- SwissProt: P09874 Human
- Unigene: 177766 Human
-
别名
- ADP ribosyltransferase diphtheria toxin like 1 antibody
- ADP ribosyltransferase NAD(+) antibody
- ADP-ribosyltransferase diphtheria toxin-like 1 antibody
see all
图片
-
Immunocytochemistry with anti-cleaved PARP1 antibody conjugated to Alexa Fluor® 488.
HeLa cells were vehicle-treated (panels A-C) or treated with 1 µM staurosporine for 4 hours (panels D-F), then fixed. Cells were treated with antigen retrieval buffer (100 mM Tris, 5% urea, pH 9.5) for 10 minutes at 95°C, then permeabilized and blocked. Cells were incubated with 1 µg/mL of the cleaved PARP1 antibody conjugated to Alexa Fluor® 488, then co-stained with the DNA stain DAPI. Images of DAPI signals (A and D), anti-cleaved PARP1 signal (B and E), and overlays of DAPI (artificially colored red for better contrast) and anti-cleaved PARP1 (colored green) images (C and F) are shown.
-
Flow cytometry with anti-cleaved PARP1 antibody conjugated to Alexa Fluor® 488.
Flow cytometric analysis was performed on HeLa vehicle-treated cells and on HeLa cells treated with 1 µM staurosporine for 4 hours. Cells were fixed with paraformaldehyde and permeablized with methanol. HeLa vehicle-treated cells were stained with 1 µg/mL of the cleaved PARP1 antibody conjugated to Alexa488 (blue) or a negative, nonreactive Alexa Fluor® 488-conjugated control antibody (black). HeLa staurosporine-treated cells were stained with 1 µg/mL of the cleaved PARP1 antibody conjugated to Alexa Fluor® 488 (yellow) or a negative, nonreactive Alexa Fluor® 488-conjugated control antibody (red). 1% BSA in PBS was used as the blocking reagent for all blocking and antibody incubation steps.
实验方案
数据表及文件
-
SDS download
-
Datasheet download
文献 (0)
ab170171 尚未被引用在任何文献中。