Human BRPF1 (Peregrin) knockout HEK-293T cell lysate
Be the first to review this product! Submit a review
|
(0 Publication)
BRPF1 KO cell lysate available now. KO validated by Western blot. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, Homozygous: 34 bp deletion in exon 2.
View Alternative Names
BR140, BRPF1_HUMAN, Bromodomain and PHD finger containing 1, Bromodomain and PHD finger-containing protein 1, Peregrin, Protein Br140, bromodomain-containing protein, 140kD
- WB
Lab
Western blot - Human BRPF1 (Peregrin) knockout HEK-293T cell lysate (AB258795)
Lane 1 : Wild-type HEK-293T cell lysate 20 μg
Lane 2 : BRPF1 knockout HEK-293T cell lysate 20 μg
Lane 3 : BRPF1 knockout HEK-293T cell lysate 20 μg
Lane 4 : Empty
Lane 5 : PC-3 cell lysate 20 μg
Lane 6 : HepG2 cell lysate 20 μg
False colour image of Western blot : Anti-Peregrin/BRPF1 antibody [EPR24069-57] staining at 1/500 dilution, shown in green; Mouse anti-Alpha Tubulin [DM1A] (ab7291) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab259840 was shown to bind specifically to Peregrin/BRPF1. A band was observed at 120 kDa in wild-type HEK-293T cell lysates with no signal observed at this size in BRPF1 knockout cell line ab266549 (knockout cell lysate ab258795). To generate this image, wild-type and BRPF1 knockout HEK-293T cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 5 % 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 (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) at 1/20000 dilution.
Lanes 1, 2, 3, 5 and 6:
Western blot - Anti-Peregrin/BRPF1 antibody [EPR24069-57] (<a href='/en-us/products/primary-antibodies/peregrin-brpf1-antibody-epr24069-57-ab259840'>ab259840</a>) at 1/500 dilution
Lane 4:
Western blot - Anti-Peregrin/BRPF1 antibody [EPR24069-57] (<a href='/en-us/products/primary-antibodies/peregrin-brpf1-antibody-epr24069-57-ab259840'>ab259840</a>)
Lane 1:
Wild-type HEK-293T cell lysate at 20 µg
Lanes 2 - 3:
BRPF1 knockout HEK-293T cell lysate at 20 µg
Lane 2:
Western blot - Human BRPF1 (Peregrin) knockout HEK-293T cell line (<a href='/en-us/products/cell-lines/human-brpf1-peregrin-knockout-hek-293t-cell-line-ab266549'>ab266549</a>)
Lane 4:
Empty
Lane 5:
PC-3 cell lysate at 20 µg
Lane 6:
HepG2 cell lysate at 20 µg
Predicted band size: 137 kDa
Observed band size: 120 kDa
false
- WB
Lab
Western blot - Human BRPF1 (Peregrin) knockout HEK-293T cell lysate (AB258795)
False colour image of Western blot : Anti-Peregrin/BRPF1 antibody - N-terminal staining at 1/500 dilution shown in green; Mouse anti-Alpha Tubulin [DM1A] (ab7291) loading control staining at 1/20000 dilution shown in red. In Western blot ab226909 was shown to bind specifically to Peregrin/BRPF1. A band was observed at 160 145 and 138 kDa in wild-type HEK-293T cell lysates with no signal observed at this size in BRPF1 knockout cell line ab266549 (knockout cell lysate ab258795). To generate this image wild-type and BRPF1 knockout HEK-293T 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 °. 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 (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) at 1/20000 dilution.
Observed bands - 160 145 and 138 kDa
All lanes:
Western blot - Anti-Peregrin/BRPF1 antibody - N-terminal (<a href='/en-us/products/primary-antibodies/peregrin-brpf1-antibody-n-terminal-ab226909'>ab226909</a>) at 1/500 dilution
Lane 1:
Wild-type HEK-293T cell lysate at 20 µg
Lane 2:
BRPF1 knockout HEK-293T cell lysate at 20 µg
Lane 2:
Western blot - Human BRPF1 (Peregrin) knockout HEK-293T cell lysate (ab258795)
Lane 2:
Western blot - Human BRPF1 (Peregrin) knockout HEK-293T cell line (<a href='/en-us/products/cell-lines/human-brpf1-peregrin-knockout-hek-293t-cell-line-ab266549'>ab266549</a>)
Lane 3:
PC-3 cell lysate at 20 µg
Lane 4:
HepG2 cell lysate at 20 µg
Predicted band size: 137 kDa
false
- Sanger seq
Unknown
Sanger Sequencing - Human BRPF1 (Peregrin) knockout HEK-293T cell lysate (AB258795)
Homozygous : 34 bp deletion in exon 2
Reactivity data
Product details
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 and ERS Genomics Limited, and is developed with patented technology. For full details of the limited use licenses and relevant patents please refer to our limited use license and patent pages.
What's included?
Properties and storage information
Gene name
Gene editing type
Gene editing method
Knockout validation
Zygosity
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Peregrin/BRPF1 is a part of the MOZ/MORF complex which is important for acetylating histone H3 at lysine 23 influencing transcriptional activation. This action aids in transcription regulation and chromatin remodeling facilitating access of transcription factors to DNA. By participating in these processes Peregrin/BRPF1 helps maintain proper gene expression patterns essential for normal cell function and development.
Pathways
BRPF1 has roles in processes like the cell cycle and embryonic development pathways because its histone acetylation influences gene expression. It interacts with other acetyltransferases such as EP300 and CREBBP which play key roles in transcription regulation and chromatin remodeling within these pathways. These interactions highlight BRPF1's critical involvement in coordinating cellular events and developmental processes.
Quality control
STR analysis
CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX
Cell culture
Biosafety level
EU: 2 US: 2
Adherent/suspension
Adherent
Gender
Female
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