Human BCL2L2 knockout HeLa cell lysate
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Human BCL2L2 knockout HeLa cell lysate suitable for Sanger seq, WB. View our extensive range of validated lysates from normal and diseased human, mouse and rat tissue.
View Alternative Names
Apoptosis regulator Bcl-W, B2CL2_HUMAN, BCL 2 Like 2, BCL W, Bcl 2 like 2 protein, Bcl-2-like protein 2, Bcl2-L-2, KIAA0271, PPP1R51, Protein phosphatase 1 regulatory subunit 51
- WB
Lab
Western blot - Human BCL2L2 knockout HeLa cell lysate (AB258325)
False colour image of Western blot : Anti-BCL2L2 antibody staining at 1/500 dilution, shown in green; loading control ab7291 (Mouse anti-Alpha Tubulin [DM1A]) staining at 1/20000 dilution, shown in red. In Western blot, the antibody was shown to bind specifically to BCL2L2. A band was observed at 17 kDa in wild-type HeLa cell lysates with no signal observed at this size in BCL2L2 knockout cell line ab265368 (knockout cell lysate ab258325). To generate this image, wild-type and BCL2L2 knockout HeLa cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in fluorescent western blot (TBS-based) blocking solution 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.
All lanes:
Anti-BCL2L2 antibody at 1/500 dilution
Lane 1:
Wild-type HeLa cell lysate at 40 µg
Lane 2:
Western blot - Human BCL2L2 knockout HeLa cell line (<a href='/en-us/products/cell-lines/human-bcl2l2-knockout-hela-cell-line-ab265368'>ab265368</a>)
Lane 2:
Western blot - Human BCL2L2 knockout HeLa cell lysate (ab258325)
Lane 2:
BCL2L2 knockout HeLa cell lysate at 40 µg
Lane 3:
HepG2 cell lysate
Lane 4:
MOLT-4 cell lysate at 40 µg
Secondary
Lanes 1 - 4:
Western blot - Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-800cw-preadsorbed-ab216773'>ab216773</a>) at 1/20000 dilution
Lanes 1 - 4:
Western blot - Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-mouse-igg-h-l-irdye-680rd-preadsorbed-ab216776'>ab216776</a>) at 1/20000 dilution
Observed band size: 17 kDa
false
- WB
Lab
Western blot - Human BCL2L2 knockout HeLa cell lysate (AB258325)
Lane 1 : Wild-type HeLa cell lysate 40 μg
Lane 2 : BCL2L2 knockout HeLa cell lysate 40 μg
Lane 3 : HepG2 cell lysate 40 μg
Lane 4 : MOLT-4 cell lysate 40 μg
False colour image of Western blot : Anti-BCL2L2 antibody staining at 1/500 dilution, shown in green; loading control ab7291 (Mouse anti-Alpha Tubulin [DM1A]) staining at 1/20000 dilution, shown in red. In Western blot, the antibody was shown to bind specifically to BCL2L2. A band was observed at 17 kDa in wild-type HeLa cell lysates with no signal observed at this size in BCL2L2 knockout cell line ab265368 (knockout cell lysate ab258325). To generate this image, wild-type and BCL2L2 knockout HeLa cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in fluorescent western blot (TBS-based) blocking solution 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.
All lanes:
anti-BCL2L2 antibody at 1/500 dilution
Lane 1:
Wild-type HeLa cell lysate at 40 µg
Lane 2:
BCL2L2 knockout HeLa cell lysate at 40 µg
Lane 2:
Western blot - Human BCL2L2 knockout HeLa cell line (<a href='/en-us/products/cell-lines/human-bcl2l2-knockout-hela-cell-line-ab265368'>ab265368</a>)
Lane 3:
HepG2 cell lysate at 40 µg
Lane 4:
MOLT-4 cell lysate at 40 µg
false
- Sanger seq
Unknown
Sanger Sequencing - Human BCL2L2 knockout HeLa cell lysate (AB258325)
Allele-1 : 1 bp insertion in exon3
- Sanger seq
Unknown
Sanger Sequencing - Human BCL2L2 knockout HeLa cell lysate (AB258325)
Allele-2 : Insertion of the selection cassette in exon3
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, 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.
What's included?
Properties and storage information
Gene name
Gene editing type
Gene editing method
Knockout validation
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
The function of Bcl-w involves its role in promoting cell survival. It is part of a complex network of interactions within the Bcl-2 family. This protein family includes both pro-apoptotic and anti-apoptotic proteins and Bcl-w helps maintain the balance by impeding apoptosis. The protein localizes to the mitochondrial outer membrane where it sequesters pro-apoptotic members such as Bax and Bak preventing the release of cytochrome c an essential step in the apoptosis process.
Pathways
The Bcl-w protein integrates into the intrinsic mitochondrial apoptosis pathway. It interacts closely with other Bcl-2 family proteins to ensure cellular homeostasis. Important pathways involving Bcl-w include the mitochondrial or intrinsic apoptosis pathway and the PI3K/AKT signaling pathway both of which regulate cell survival. Related proteins include Bcl-2 Bcl-XL Bax and Bak. These proteins collectively modulate the apoptosis signaling and therefore influence cell fate decisions within tissues where Bcl-w is expressed.
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 protocols
- Visit the General protocols
- Visit the Troubleshooting
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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