Anti-KMT6 / EZH2 antibody [EPR20108] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
- 각 태그의 뜻
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(2 제품이 사용된 논문 )
- IP
Supplier Data
Immunoprecipitation - Anti-KMT6 / EZH2 antibody [EPR20108] - BSA and Azide free (AB240992)
KMT6 / EZH2 was immunoprecipitated from 0.35 mg of HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate with ab191250 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab191250 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/10000 dilution.
Lane 1 : HeLa whole cell lysate 10 μg (Input).
Lane 2 : ab191250 IP in HeLa whole cell lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab191250 in HeLa whole cell lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 3 minutes.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab191250).
All lanes:
Immunoprecipitation - Anti-KMT6 / EZH2 antibody [EPR20108] - ChIP Grade (<a href='/ko/products/primary-antibodies/kmt6-ezh2-antibody-epr20108-chip-grade-ab191250'>ab191250</a>)
Predicted band size: 85 kDa
false
- WB
Supplier Data
Western blot - Anti-KMT6 / EZH2 antibody [EPR20108] - BSA and Azide free (AB240992)
Merged signal (red and green). Green - ab191250 observed at 93 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab191250 was shown to specifically recognize KMT6/EZH2 in wild-type HAP1 cells along with additional cross-reactive bands. No band was observed when KMT6/EZH2 knockout samples were examined. Wild-type and KMT6/EZH2 knockout samples were subjected to SDS-PAGE. ab191250 and ab8245 (loading control to GAPDH) were diluted at 1/1000 and 1/10,000 respectively and incubated overnight at 4°C. 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 1/10,000 dilution for 1 hour at room temperature before imaging.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab191250).
All lanes:
Western blot - Anti-KMT6 / EZH2 antibody [EPR20108] - ChIP Grade (<a href='/ko/products/primary-antibodies/kmt6-ezh2-antibody-epr20108-chip-grade-ab191250'>ab191250</a>) at 1/1000 dilution
Lane 1:
Wild-type HAP1 cell lysate at 20 µg
Lane 2:
KMT6 / EZH2 knockout HAP1 cell lysate at 20 µg
Lane 3:
HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate at 20 µg
Lane 4:
MCF7 (human breast adenocarcinoma cell line) whole cell lysate at 20 µg
Predicted band size: 85 kDa
Observed band size: 90 kDa
false
- WB
Lab
Western blot - Anti-KMT6 / EZH2 antibody [EPR20108] - BSA and Azide free (AB240992)
False colour image of Western blot : Anti-KMT6 / EZH2 antibody [EPR20108] - ChIP Grade staining at 1/1000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab191250 was shown to bind specifically to KMT6 / EZH2. A band was observed at 90 kDa in wild-type MCF7 cell lysates with no signal observed at this size in ezh2 CRISPR-Cas9 edited cell line ab281611 (CRISPR-Cas9 edited cell lysate ab282963). The band observed in the CRISPR-Cas9 edited lysate lane below 90 kDa is likely to represent a truncated form of KMT6 / EZH2. This has not been investigated further and the functional properties of the gene product have not been determined. To generate this image, wild-type and ezh2 CRISPR-Cas9 edited MCF7 cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3 % milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution.
All lanes:
Western blot - Anti-KMT6 / EZH2 antibody [EPR20108] - ChIP Grade (<a href='/ko/products/primary-antibodies/kmt6-ezh2-antibody-epr20108-chip-grade-ab191250'>ab191250</a>) at 1/1000 dilution
Lane 1:
Wild-type MCF7 cell lysate at 20 µg
Lane 2:
ezh2 CRISPR-Cas9 edited MCF7 cell lysate at 20 µg
Lane 3:
HEK-293 cell lysate at 20 µg
Lane 4:
Mouse Testis cell lysate at 20 µg
Observed band size: 90 kDa
false
관련 conjugated 항체와 다양한 조성의 항체 (1)
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Anti-KMT6 / EZH2 antibody [EPR20108] - ChIP Grade
Reactivity 정보
제품 세부 정보
ab240992 is the carrier-free version of ab191250.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
특성 및 보관 정보
제형
Purification 테크닉
보관 버퍼
배송 시 보관 조건
적절한 단기 보관 조건
적절한 장기 보관 조건
보관 정보
추가 정보
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
EZH2 plays a central role in regulating gene expression during development and differentiation. It is a core component of the PRC2 complex which includes other proteins such as EED and SUZ12. Through its catalytic activity EZH2 contributes to the maintenance of the transcriptionally repressed state of genes influencing processes such as cell identity and proliferation. In many cell types EZH2-mediated gene silencing is necessary for normal development and dysregulation can lead to aberrant cellular processes.
Pathways
EZH2 participates in key regulatory networks notably the Wnt signaling pathway and the p53 pathway. Within the Wnt pathway EZH2's activity contributes to controlling gene expression that influences cellular differentiation and proliferation. Meanwhile interaction with the p53 pathway can impact the cellular response to stress and DNA damage highlighting EZH2’s regulatory dimension. Other proteins like β-catenin in the Wnt pathway interact with EZH2 reflecting its integration in these complex signaling networks.
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타겟 정보
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제품이 사용된 논문 (2)
Recent publications for all applications. Explore the 전체 목록 and refine your search
Respiratory research 25:119 PubMed38459541
2024
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Molecular therapy. Nucleic acids 24:1012-1023 PubMed34141456
2021
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Product promise
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