人PPP2R5E knockout HeLa cell裂解物
Human PPP2R5E knockout HeLa cell lysate
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PPP2R5E KO cell lysate available now. KO validated by Western blot. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, 1 bp deletion in exon2 and Insertion of the selection cassette in exon2.
查看别名
2A5E_HUMAN, Epsilon isoform of regulatory subunit B56 protein phosphatase 2A, PP2A B subunit B' epsilon, PP2A B subunit B' epsilon isoform, PP2A B subunit B56 epsilon, PP2A B subunit B56 epsilon isoform, PP2A B subunit PR61 epsilon, PP2A B subunit PR61 epsilon isoform, PP2A B subunit R5 epsilon, PP2A B subunit R5 epsilon isoform, PP2A B subunit isoform B''-epsilon, PP2A B subunit isoform B'-epsilon, PP2A B subunit isoform B56-epsilon, PP2A B subunit isoform PR61-epsilon, PP2A B subunit isoform R5-epsilon, PPP2R5E, Protein phosphatase 2 regulatory subunit B (B56) epsilon isoform, Protein phosphatase 2 regulatory subunit B' epsilon, Protein phosphatase 2 regulatory subunit B' epsilon isoform, Regulatory subunit B of protein phosphatase 2 epsilon isoform, Serine/threonine protein phosphatase 2A 56 kDa regulatory subunit epsilon, Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit epsilon isoform
- WB
Lab
Western blot - Human PPP2R5E knockout HeLa cell lysate (AB258135)
Lane 1 : Wild-type HeLa cell lysate (20 μg)
Lane 2 : PPP2R5E knockout HeLa cell lysate (20 μg)
Lane 3 : HEK-293 cell lysate (20 μg)
Lane 4 : Daudi cell lysate (20 μg)
Lanes 1-4 : Merged signal (red and green). Green - ab198290 observed at 55 kDa. Red - loading control ab8245 observed at 37 kDa.
ab198290 Anti-PPP2R5E antibody [EPR17146] was shown to specifically react with PPP2R5E in wild-type HeLa cells. Loss of signal was observed when knockout cell line ab265637 (knockout cell lysate ab258135) was used. Wild-type and PPP2R5E knockout samples were subjected to SDS-PAGE. ab198290 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 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-PPP2R5E antibody [EPR17146] (<a href='/products/primary-antibodies/ppp2r5e-antibody-epr17146-ab198290'>ab198290</a>) at 1/1000 dilution
Lane 1:
Wild-type HeLa cell lysate at 20 µg
Lane 2:
PPP2R5E knockout HeLa cell lysate at 20 µg
Lane 2:
Western blot - Human PPP2R5E knockout HeLa cell line (<a href='/products/cell-lines/human-ppp2r5e-knockout-hela-cell-line-ab265637'>ab265637</a>)
Lane 3:
HEK-293 cell lysate at 20 µg
Lane 4:
Daudi cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-800cw-preadsorbed-ab216773'>ab216773</a>) at 1/20000 dilution
Predicted band size: 55 kDa
Observed band size: 55 kDa
false
- WB
Lab
Western blot - Human PPP2R5E knockout HeLa cell lysate (AB258135)
Lane 1 : Wild-type HeLa cell lysate (20 μg)
Lane 2 : PPP2R5E knockout HeLa cell lysate (20 μg)
Lane 3 : HEK-293 cell lysate (20 μg)
Lane 4 : Daudi cell lysate (20 μg)
Lanes 1-4 : Merged signal (red and green). Green - ab198500 observed at 55 kDa. Red - loading control ab8245 observed at 37 kDa.
ab198500 Recombinant Anti-PPP2R5E antibody [EPR17147] - C-terminal was shown to specifically react with PPP2R5E in wild-type HeLa cells. Loss of signal was observed when knockout cell line ab265637 (knockout cell lysate ab258135) was used. Wild-type and PPP2R5E knockout samples were subjected to SDS-PAGE. ab198500 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated overnight at 4°C at 1 in 5000 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 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-PPP2R5E antibody [EPR17147] - C-terminal (<a href='/products/primary-antibodies/ppp2r5e-antibody-epr17147-c-terminal-ab198500'>ab198500</a>) at 1/5000 dilution
Lane 1:
Wild-type HeLa cell lysate at 20 µg
Lane 2:
PPP2R5E knockout HeLa cell lysate at 20 µg
Lane 2:
Western blot - Human PPP2R5E knockout HeLa cell line (<a href='/products/cell-lines/human-ppp2r5e-knockout-hela-cell-line-ab265637'>ab265637</a>)
Lane 3:
HEK-293T cell lysate at 20 µg
Lane 4:
Daudi cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-800cw-preadsorbed-ab216773'>ab216773</a>) at 1/20000 dilution
Predicted band size: 55 kDa
Observed band size: 55 kDa
false
- Sanger seq
Unknown
Sanger Sequencing - Human PPP2R5E knockout HeLa cell lysate (AB258135)
Allele-2 : Insertion of the selection cassette in exon2
- Sanger seq
Unknown
Sanger Sequencing - Human PPP2R5E knockout HeLa cell lysate (AB258135)
Allele-1 : 1 bp deletion in exon2
反应性数据
产品详情
Knockout cell lysate achieved by CRISPR/Cas9.
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.
Lysate preparation: Our lysates are made using RIPA buffer to which we add a protease inhibitor cocktail and phosphatase inhibitor cocktail (ratio: 300:100:10). This means that the protein of interest is denatured. If you require a native form of the protein please use the live cell version. Please refer to our lysis protocol for further details on how our lysates are prepared.
User storage instructions: Lyophilizate may be stored at 4°C. After reconstitution, store at -20°C for short-term storage or -80°C for long-term storage.
This product is subject to limited use licenses from The Broad Institute, ERS Genomics Limited and Sigma-Aldrich Co. LLC, and is developed with patented technology. For full details of the licenses and patents please refer to our limited use license and patent pages.
规格
性能和储存信息
基因名称
基因编辑类型
基因编辑方法
敲除验证
运输条件
推荐的短期储存条件
推荐的长期储存条件
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
PPP2R5E plays a role in regulating cell growth and division. It is a part of the PP2A holoenzyme complex acting as a critical modulatory component. By associating with the PP2A core enzyme PPP2R5E contributes to the dephosphorylation process of many substrates. These substrates are vital for maintaining cellular functions such as signal transduction and cell cycle progression.
Pathways
PPP2R5E takes part in cell signaling and apoptotic pathways. It has substantial involvement in the MAPK signaling pathway where it modulates the activity of related kinases. PPP2R5E interacts with proteins like RAF1 influencing the pathway's function. Additionally it also participates in the Wnt signaling pathway where its regulatory role impacts cellular differentiation and proliferation.
质量控制
STR 分析
CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX
细胞培养
生物安全等级
EU: 2 US: 2
贴壁/悬浮
Adherent
性别
Female
Abcam Product Promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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