人H2A.X (phospho S139) In-Cell ELISA试剂盒(IR)
Human H2A.X (phospho S139) In-Cell ELISA Kit (IR)
Be the first to review this product! Submit a review
|
(3 Publications)
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Human H2A.X (phospho S139) In-Cell ELISA Kit (IR) (AB131382)
Specificity of H2A.X (phospho S139) antibodies demonstrated by immunocytochemistry. The primary antibody used in this assay kit was validated by staining HeLa cells treated with 10 μM Camptothecin or vehicle for 4 hours and imaged by fluorescent microscopy. Note the absence of H2A.X (phospho S139) in the untreated cells.
- In-Cell ELISA
Supplier Data
In-Cell ELISA - Human H2A.X (phospho S139) In-Cell ELISA Kit (IR) (AB131382)
Sample experiment using ab131382 on HeLa cells following drug treatment : H2A.X (phospho S139) readout. HeLa cells were treated for 4 hours with dose titrations of Camptothecin, Etoposide and Staurosporin. The dashed grey line indicates the vehicle control signal.
- WB
Supplier Data
Western blot - Human H2A.X (phospho S139) In-Cell ELISA Kit (IR) (AB131382)
Antibody specificity demonstrated by Western Blot Analysis. Whole cell lysates from Jurkat cells were analyzed by western blot with the H2A.X (phospho S139) antibody used in this assay kit.
false
- WB
Supplier Data
Western blot - Human H2A.X (phospho S139) In-Cell ELISA Kit (IR) (AB131382)
Antibody specificity demonstrated by Western Blot Analysis : H2A.X (phospho S139) is phospho-specific. Jurkat cells were stimulated with UV light exposure to induce H2A.X (phospho S139) and then the UV treated lysate was treated with lambda protein phosphatase. Top panel : H2A.X (phospho S139) is induced by UV treatment and the western blot band is sensitive to phosphatase treatment. Lower panel : In contrast, total H2A.X (ab124781) levels are not sensitive to phosphatase treatment.
false
反应性数据
产品详情
The H2A.X (phospho S139) Human In-Cell ELISA Kit (IR) (ab131382) is designed to study the induction of DNA damage in response to various stimuli. A rabbit monoclonal antibody specific to H2A.X phospho S139 is used in this high-throughput duplexing plate-based assay. H2A.X (phospho S139) is a reliable readout for double-stranded DNA breaks.
Plates are available in our ICE (In-Cell ELISA) Support Pack (ab111542) which can be bought seperately.
In-Cell ELISA (ICE) technology is used to perform quantitative immunocytochemistry of cultured cells with a near-infrared fluorescent dye-labeled detector antibody. The technique generates quantitative data with specificity similar to western blotting, but with much greater quantitative precision and higher throughput due to the greater dynamic range and linearity of direct fluorescence detection and the ability to run up to 96 samples in parallel.
This method rapidly fixes the cells in situ, stabilizing the in vivo levels of proteins and their posttranslational modifications, and thus essentially eliminates changes during sample handling, such as preparation of protein extracts. Finally, the H2A.X (phospho S139) signal can be normalized to cell amount, measured by the provided Janus Green whole-cell stain, to further increase the assay precision.
This product is designed for LI-COR® Odyssey® or Aerius® infrared imaging systems.
REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.
精确度
规格
性能和储存信息
运输条件
推荐的短期储存条件
推荐的长期储存条件
储存信息
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
H2A.X pSer139 serves as an indicator of DNA repair processes and contributes to maintaining genomic stability. When DNA damage occurs H2A.X rapidly phosphorylates and forms part of a complex including other repair proteins like MDC1 and 53BP1 marking regions for DNA repair machinery. By localizing with damaged DNA H2A.X pSer139 helps prevent genome instability by coordinating repair responses such as homologous recombination and non-homologous end joining.
Pathways
H2A.X pSer139 plays a significant role in the DNA damage response (DDR) and cell cycle checkpoint pathways. Within the ATM/ATR signaling pathway phosphorylation of H2A.X is an early step triggering cellular checkpoint controls and DNA repair. Proteins like ATM a kinase activated by DNA damage interact with H2A.X pSer139 phosphorylating it to initiate recruitment of repair complexes. Furthermore H2A.X pSer139 links with CHK2 a protein kinase in the DDR pathway helping regulate the cell cycle in response to DNA damage.
靶点信息
文献 (3)
Recent publications for all applications. Explore the full list and refine your search
Current issues in molecular biology 45:7915-7932 PubMed37886943
2023
Applications
Unspecified application
Species
Unspecified reactive species
Scientific reports 9:14135 PubMed31575977
2019
Applications
Unspecified application
Species
Unspecified reactive species
Molecular cancer therapeutics 13:2817-26 PubMed25253786
2014
Applications
Unspecified application
Species
Unspecified reactive species
Abcam Product Promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com